Expression of PTPRO in the interneurons of adult mouse olfactory bulb

PTPRO is a receptor‐type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III‐like domains in its extracellular region. In the chick, PTPRO mRNA has been shown to be particularly abundant in embryonic brain, and PTPRO is implic...

Full description

Saved in:
Bibliographic Details
Published inJournal of comparative neurology (1911) Vol. 518; no. 2; pp. 119 - 136
Main Authors Kotani, Takenori, Murata, Yoji, Ohnishi, Hiroshi, Mori, Munemasa, Kusakari, Shinya, Saito, Yasuyuki, Okazawa, Hideki, Bixby, John L., Matozaki, Takashi
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.01.2010
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
Abstract PTPRO is a receptor‐type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III‐like domains in its extracellular region. In the chick, PTPRO mRNA has been shown to be particularly abundant in embryonic brain, and PTPRO is implicated in axon growth and guidance during embryonic development. However, the temporal and spatial expression of PTPRO protein in the mammalian CNS, particularly in the juvenile and adult mammalian brain, has not been evaluated in any detail. By immunohistofluorescence analysis with a monoclonal antibody to PTPRO, we show that PTPRO is widely expressed throughout the mouse brain from embryonic day 16 to postnatal day 1, while expression is largely confined to the olfactory bulb (OB) and olfactory tubercle in the adult brain. In the OB, PTPRO protein is expressed predominantly in the external plexiform layer, the granule cell layer, and the glomerular layer (GL). In these regions, expression of PTPRO is predominant in interneurons such as γ‐aminobutyric acid (GABA)‐ergic or calretinin (CR)‐positive granule cells. In addition, PTPRO is expressed in GABAergic, CR‐positive, tyrosine hydroxylase‐positive, or neurocalcin‐positive periglomerular cells in the GL. Costaining of PTPRO with other neuronal markers suggests that PTPRO is likely to be localized to the dendrites or dendritic spines of these olfactory interneurons. Thus, PTPRO might participate in regulation of dendritic morphology or synapse formation of interneurons in the adult mouse OB. J. Comp. Neurol. 518:119–136, 2010. © 2009 Wiley‐Liss, Inc.
AbstractList PTPRO is a receptor-type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III-like domains in its extracellular region. In the chick, PTPRO mRNA has been shown to be particularly abundant in embryonic brain, and PTPRO is implicated in axon growth and guidance during embryonic development. However, the temporal and spatial expression of PTPRO protein in the mammalian CNS, particularly in the juvenile and adult mammalian brain, has not been evaluated in any detail. By immunohistofluorescence analysis with a monoclonal antibody to PTPRO, we show that PTPRO is widely expressed throughout the mouse brain from embryonic day 16 to postnatal day 1, while expression is largely confined to the olfactory bulb (OB) and olfactory tubercle in the adult brain. In the OB, PTPRO protein is expressed predominantly in the external plexiform layer, the granule cell layer, and the glomerular layer (GL). In these regions, expression of PTPRO is predominant in interneurons such as gamma-aminobutyric acid (GABA)-ergic or calretinin (CR)-positive granule cells. In addition, PTPRO is expressed in GABAergic, CR-positive, tyrosine hydroxylase-positive, or neurocalcin-positive periglomerular cells in the GL. Costaining of PTPRO with other neuronal markers suggests that PTPRO is likely to be localized to the dendrites or dendritic spines of these olfactory interneurons. Thus, PTPRO might participate in regulation of dendritic morphology or synapse formation of interneurons in the adult mouse OB.
PTPRO is a receptor‐type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III‐like domains in its extracellular region. In the chick, PTPRO mRNA has been shown to be particularly abundant in embryonic brain, and PTPRO is implicated in axon growth and guidance during embryonic development. However, the temporal and spatial expression of PTPRO protein in the mammalian CNS, particularly in the juvenile and adult mammalian brain, has not been evaluated in any detail. By immunohistofluorescence analysis with a monoclonal antibody to PTPRO, we show that PTPRO is widely expressed throughout the mouse brain from embryonic day 16 to postnatal day 1, while expression is largely confined to the olfactory bulb (OB) and olfactory tubercle in the adult brain. In the OB, PTPRO protein is expressed predominantly in the external plexiform layer, the granule cell layer, and the glomerular layer (GL). In these regions, expression of PTPRO is predominant in interneurons such as γ‐aminobutyric acid (GABA)‐ergic or calretinin (CR)‐positive granule cells. In addition, PTPRO is expressed in GABAergic, CR‐positive, tyrosine hydroxylase‐positive, or neurocalcin‐positive periglomerular cells in the GL. Costaining of PTPRO with other neuronal markers suggests that PTPRO is likely to be localized to the dendrites or dendritic spines of these olfactory interneurons. Thus, PTPRO might participate in regulation of dendritic morphology or synapse formation of interneurons in the adult mouse OB. J. Comp. Neurol. 518:119–136, 2010. © 2009 Wiley‐Liss, Inc.
Abstract PTPRO is a receptor‐type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III‐like domains in its extracellular region. In the chick, PTPRO mRNA has been shown to be particularly abundant in embryonic brain, and PTPRO is implicated in axon growth and guidance during embryonic development. However, the temporal and spatial expression of PTPRO protein in the mammalian CNS, particularly in the juvenile and adult mammalian brain, has not been evaluated in any detail. By immunohistofluorescence analysis with a monoclonal antibody to PTPRO, we show that PTPRO is widely expressed throughout the mouse brain from embryonic day 16 to postnatal day 1, while expression is largely confined to the olfactory bulb (OB) and olfactory tubercle in the adult brain. In the OB, PTPRO protein is expressed predominantly in the external plexiform layer, the granule cell layer, and the glomerular layer (GL). In these regions, expression of PTPRO is predominant in interneurons such as γ‐aminobutyric acid (GABA)‐ergic or calretinin (CR)‐positive granule cells. In addition, PTPRO is expressed in GABAergic, CR‐positive, tyrosine hydroxylase‐positive, or neurocalcin‐positive periglomerular cells in the GL. Costaining of PTPRO with other neuronal markers suggests that PTPRO is likely to be localized to the dendrites or dendritic spines of these olfactory interneurons. Thus, PTPRO might participate in regulation of dendritic morphology or synapse formation of interneurons in the adult mouse OB. J. Comp. Neurol. 518:119–136, 2010. © 2009 Wiley‐Liss, Inc.
PTPRO is a receptor-type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III-like domains in its extracellular region. In the chick, PTPRO mRNA has been shown to be particularly abundant in embryonic brain, and PTPRO is implicated in axon growth and guidance during embryonic development. However, the temporal and spatial expression of PTPRO protein in the mammalian CNS, particularly in the juvenile and adult mammalian brain, has not been evaluated in any detail. By immunohistofluorescence analysis with a monoclonal antibody to PTPRO, we show that PTPRO is widely expressed throughout the mouse brain from embryonic day 16 to postnatal day 1, while expression is largely confined to the olfactory bulb (OB) and olfactory tubercle in the adult brain. In the OB, PTPRO protein is expressed predominantly in the external plexiform layer, the granule cell layer, and the glomerular layer (GL). In these regions, expression of PTPRO is predominant in interneurons such as [gamma]-aminobutyric acid (GABA)-ergic or calretinin (CR)-positive granule cells. In addition, PTPRO is expressed in GABAergic, CR-positive, tyrosine hydroxylase-positive, or neurocalcin-positive periglomerular cells in the GL. Costaining of PTPRO with other neuronal markers suggests that PTPRO is likely to be localized to the dendrites or dendritic spines of these olfactory interneurons. Thus, PTPRO might participate in regulation of dendritic morphology or synapse formation of interneurons in the adult mouse OB. J. Comp. Neurol. 518:119-136, 2010. © 2009 Wiley-Liss, Inc.
PTPRO is a receptor-type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III-like domains in its extracellular region. In the chick, PTPRO mRNA has been shown to be particularly abundant in embryonic brain, and PTPRO is implicated in axon growth and guidance during embryonic development. However, the temporal and spatial expression of PTPRO protein in the mammalian CNS, particularly in the juvenile and adult mammalian brain, has not been evaluated in any detail. By immunohistofluorescence analysis with a monoclonal antibody to PTPRO, we show that PTPRO is widely expressed throughout the mouse brain from embryonic day 16 to postnatal day 1, while expression is largely confined to the olfactory bulb (OB) and olfactory tubercle in the adult brain. In the OB, PTPRO protein is expressed predominantly in the external plexiform layer, the granule cell layer, and the glomerular layer (GL). In these regions, expression of PTPRO is predominant in interneurons such as γ-aminobutyric acid (GABA)-ergic or calretinin (CR)-positive granule cells. In addition, PTPRO is expressed in GABAergic, CR-positive, tyrosine hydroxylase-positive, or neurocalcin-positive periglomerular cells in the GL. Costaining of PTPRO with other neuronal markers suggests that PTPRO is likely to be localized to the dendrites or dendritic spines of these olfactory interneurons. Thus, PTPRO might participate in regulation of dendritic morphology or synapse formation of interneurons in the adult mouse OB.
PTPRO is a receptor-type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III-like domains in its extracellular region. In the chick, PTPRO mRNA has been shown to be particularly abundant in embryonic brain, and PTPRO is implicated in axon growth and guidance during embryonic development. However, the temporal and spatial expression of PTPRO protein in the mammalian CNS, particularly in the juvenile and adult mammalian brain, has not been evaluated in any detail. By immunohistofluorescence analysis with a monoclonal antibody to PTPRO, we show that PTPRO is widely expressed throughout the mouse brain from embryonic day 16 to postnatal day 1, while expression is largely confined to the olfactory bulb (OB) and olfactory tubercle in the adult brain. In the OB, PTPRO protein is expressed predominantly in the external plexiform layer, the granule cell layer, and the glomerular layer (GL). In these regions, expression of PTPRO is predominant in interneurons such as -aminobutyric acid (GABA)-ergic or calretinin (CR)-positive granule cells. In addition, PTPRO is expressed in GABAergic, CR-positive, tyrosine hydroxylase-positive, or neurocalcin-positive periglomerular cells in the GL. Costaining of PTPRO with other neuronal markers suggests that PTPRO is likely to be localized to the dendrites or dendritic spines of these olfactory interneurons. Thus, PTPRO might participate in regulation of dendritic morphology or synapse formation of interneurons in the adult mouse OB. J. Comp. Neurol. 518:119-136, 2010.
Author Murata, Yoji
Saito, Yasuyuki
Kotani, Takenori
Bixby, John L.
Ohnishi, Hiroshi
Okazawa, Hideki
Mori, Munemasa
Kusakari, Shinya
Matozaki, Takashi
AuthorAffiliation 1 Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
2 Department of Molecular and Cellular Pharmacology, and Neuroscience Program, The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Lois Pope LIFE Center, Miami, Florida 33136
AuthorAffiliation_xml – name: 2 Department of Molecular and Cellular Pharmacology, and Neuroscience Program, The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Lois Pope LIFE Center, Miami, Florida 33136
– name: 1 Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
Author_xml – sequence: 1
  givenname: Takenori
  surname: Kotani
  fullname: Kotani, Takenori
  organization: Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
– sequence: 2
  givenname: Yoji
  surname: Murata
  fullname: Murata, Yoji
  organization: Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
– sequence: 3
  givenname: Hiroshi
  surname: Ohnishi
  fullname: Ohnishi, Hiroshi
  organization: Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
– sequence: 4
  givenname: Munemasa
  surname: Mori
  fullname: Mori, Munemasa
  organization: Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
– sequence: 5
  givenname: Shinya
  surname: Kusakari
  fullname: Kusakari, Shinya
  organization: Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
– sequence: 6
  givenname: Yasuyuki
  surname: Saito
  fullname: Saito, Yasuyuki
  organization: Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
– sequence: 7
  givenname: Hideki
  surname: Okazawa
  fullname: Okazawa, Hideki
  organization: Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
– sequence: 8
  givenname: John L.
  surname: Bixby
  fullname: Bixby, John L.
  organization: Department of Molecular and Cellular Pharmacology, and Neuroscience Program, The Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Lois Pope LIFE Center, Miami, Florida 33136
– sequence: 9
  givenname: Takashi
  surname: Matozaki
  fullname: Matozaki, Takashi
  email: matozaki@showa.gunma-u.ac.jp
  organization: Laboratory of Biosignal Sciences, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Gunma 371-8512, Japan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/19924828$$D View this record in MEDLINE/PubMed
BookMark eNqFkUtvEzEURi1URNPCgj-ARmKBWEzr92ODVEJoQVVaQRHsLI9zh06Z2MGegebf4zahPCTE6i6-c498_e2hnRADIPSY4AOCMT30AQ4opczcQxOCjayNlmQHTUpGamOk2kV7OV9hjI1h-gHaJcZQrqmeoNnsepUg5y6GKrbV-cX5u7OqC9VwCWUMkAKMKYZ8E7rF2A_VMo4Zqti3zg8xratm7JuH6H7r-gyPtnMffXg9u5ie1Kdnx2-mR6e1F0qbmlFMWSsVZwIDAUUWUtCm0UJqLRxRzji2oEJ7pRgHzqV3mhjVAmu951SwffRi412NzRIWHsKQXG9XqVu6tLbRdfbPJHSX9nP8ZplhTGldBM-2ghS_jpAHu-yyh753AcpdVgkuBGUY_59knEiJb8mnf5FXcUyh_IMlWkoqiZG8UM83lE8x5wTt3asJtjct2tKivW2xsE9-P_MXua2tAIcb4HvXw_rfJjudz34q681Glwe4vttw6YuViilhP86PLXs1Ny8_nby179kPjDC12w
CitedBy_id crossref_primary_10_1016_j_cellsig_2010_07_001
crossref_primary_10_1016_j_jpsychires_2011_11_001
crossref_primary_10_1007_s00018_013_1259_7
crossref_primary_10_3389_fnana_2022_1097467
crossref_primary_10_1016_j_bbadis_2024_167141
crossref_primary_10_1016_j_bbrc_2018_03_064
crossref_primary_10_1111_ejn_15075
crossref_primary_10_3389_fgene_2022_825974
crossref_primary_10_1016_j_aanat_2021_151881
crossref_primary_10_3390_ani12091079
crossref_primary_10_1523_JNEUROSCI_0729_17_2017
crossref_primary_10_1074_jbc_M113_529503
crossref_primary_10_1111_j_1365_2443_2010_01398_x
crossref_primary_10_1523_JNEUROSCI_4707_12_2013
crossref_primary_10_1172_jci_insight_166306
Cites_doi 10.1016/j.pnpbp.2004.05.025
10.1038/nn1697
10.1523/JNEUROSCI.14-03-01834.1994
10.1007/s00018-003-3123-7
10.1523/JNEUROSCI.4531-04.2005
10.1523/JNEUROSCI.3981-06.2006
10.1096/fj.05-4826fje
10.1016/S0925-4773(98)00119-1
10.1083/jcb.200106025
10.1083/jcb.200306033
10.1016/S0168-0102(98)00002-9
10.1038/79162
10.1006/bbrc.2000.3584
10.1016/j.tins.2005.03.005
10.1002/neu.10284
10.1128/MCB.21.21.7117-7136.2001
10.1016/j.semcdb.2006.04.006
10.1002/(SICI)1097-4695(199904)39:1<81::AID-NEU7>3.0.CO;2-K
10.1101/gad.1256405
10.1111/j.1471-4159.2008.05416.x
10.1002/cne.21909
10.1002/cne.20437
10.1002/cne.20896
10.1111/j.1365-2443.2008.01270.x
10.1016/j.tcb.2008.07.002
10.1097/01.ASN.0000130167.30769.55
10.1083/jcb.200809151
10.1007/s11068-005-8355-z
10.1002/cne.20758
10.1016/j.cell.2004.05.018
10.1002/jnr.10457
10.1042/bj3160515
10.1074/jbc.M400950200
10.1385/JMN:29:3:241
10.1083/jcb.200105019
10.1128/MCB.20.13.4791-4805.2000
10.1016/S0021-9258(17)32113-0
10.1042/bj3210865
10.1523/JNEUROSCI.1633-07.2007
10.1523/JNEUROSCI.5625-07.2008
10.1523/JNEUROSCI.2870-06.2007
10.1002/cne.10532
10.1016/j.brainresrev.2006.04.006
10.1016/j.conb.2008.04.001
10.1172/JCI7236
10.1093/oxfordjournals.jbchem.a003205
10.1016/S0165-3806(00)00136-X
10.1242/dev.116.1.201
10.1016/j.tcb.2007.06.006
10.1182/blood.V94.7.2403.419k39_2403_2413
10.1002/cne.10371
10.1016/S0092-8674(01)00314-2
10.1002/dneu.20389
10.1002/cne.21205
10.1002/(SICI)1097-4695(199611)31:3<309::AID-NEU4>3.0.CO;2-E
10.1074/jbc.270.45.27339
10.1016/0304-3940(96)12640-9
ContentType Journal Article
Copyright Copyright © 2009 Wiley‐Liss, Inc.
Copyright © 2009 Wiley-Liss, Inc.
2009 Wiley-Liss, Inc. 2009
Copyright_xml – notice: Copyright © 2009 Wiley‐Liss, Inc.
– notice: Copyright © 2009 Wiley-Liss, Inc.
– notice: 2009 Wiley-Liss, Inc. 2009
DBID BSCLL
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7QR
7TK
8FD
FR3
K9.
P64
7X8
5PM
DOI 10.1002/cne.22239
DatabaseName Istex
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
Chemoreception Abstracts
Neurosciences Abstracts
Technology Research Database
Engineering Research Database
ProQuest Health & Medical Complete (Alumni)
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
ProQuest Health & Medical Complete (Alumni)
Chemoreception Abstracts
Engineering Research Database
Technology Research Database
Neurosciences Abstracts
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
DatabaseTitleList MEDLINE

CrossRef
ProQuest Health & Medical Complete (Alumni)

Chemoreception Abstracts
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Zoology
EISSN 1096-9861
EndPage 136
ExternalDocumentID 4312893141
10_1002_cne_22239
19924828
CNE22239
ark_67375_WNG_3DN9BXHJ_S
Genre article
Research Support, Non-U.S. Gov't
Journal Article
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: National Institutes of Health
  funderid: NS38920
– fundername: The Ministry of Education, Culture, Sports, Science, and Technology of Japan
  funderid: 20370044; 1979025
– fundername: NINDS NIH HHS
  grantid: NS38920
– fundername: NINDS NIH HHS
  grantid: R01 NS038920
– fundername: National Institute of Neurological Disorders and Stroke : NINDS
  grantid: R01 NS038920 || NS
GroupedDBID ---
-DZ
-~X
.3N
.GA
.Y3
05W
0R~
10A
123
1L6
1OB
1OC
1ZS
31~
33P
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
5RE
5VS
66C
702
79B
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABIJN
ABIVO
ABJNI
ABOCM
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFS
ACIWK
ACPOU
ACPRK
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
AEEZP
AEIGN
AEIMD
AELAQ
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFNX
AFFPM
AFGKR
AFPWT
AFZJQ
AHBTC
AHMBA
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ASPBG
ATUGU
AUFTA
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BSCLL
BY8
C45
CS3
D-E
D-F
DCZOG
DPXWK
DR1
DR2
DRFUL
DRSTM
DU5
EBS
EJD
F00
F01
F04
F5P
FEDTE
G-S
G.N
GNP
GODZA
H.T
H.X
HBH
HF~
HGLYW
HHY
HHZ
HVGLF
HZ~
IX1
J0M
JPC
KQQ
L7B
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OVD
P2P
P2W
P2X
P4D
PALCI
PQQKQ
Q.N
Q11
QB0
QRW
R.K
ROL
RWD
RWI
RX1
RYL
SUPJJ
TEORI
UB1
V2E
W8V
W99
WBKPD
WIB
WIH
WIK
WJL
WNSPC
WOHZO
WQJ
WRC
WUP
WXSBR
WYISQ
XG1
XV2
YQT
ZZTAW
~IA
~WT
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7QR
7TK
8FD
FR3
K9.
P64
7X8
5PM
ID FETCH-LOGICAL-c5789-32023f674350e1e71d652bb856885a17a9a3d258c7734e446ca8197fe3fcc4253
IEDL.DBID DR2
ISSN 0021-9967
IngestDate Tue Sep 17 21:18:19 EDT 2024
Fri Aug 16 02:35:18 EDT 2024
Fri Aug 16 04:11:04 EDT 2024
Thu Oct 10 18:37:45 EDT 2024
Fri Aug 23 03:41:18 EDT 2024
Sat Sep 28 07:45:55 EDT 2024
Sat Aug 24 00:53:42 EDT 2024
Wed Oct 30 10:04:00 EDT 2024
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 2
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c5789-32023f674350e1e71d652bb856885a17a9a3d258c7734e446ca8197fe3fcc4253
Notes The Ministry of Education, Culture, Sports, Science, and Technology of Japan - No. 20370044; No. 1979025
istex:C26F7E5D05FA5A4BC5ED9EE9DA267CD362120419
ark:/67375/WNG-3DN9BXHJ-S
ArticleID:CNE22239
National Institutes of Health - No. NS38920
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Article-2
ObjectType-Feature-1
OpenAccessLink https://europepmc.org/articles/pmc3933788?pdf=render
PMID 19924828
PQID 1866261964
PQPubID 1006438
PageCount 18
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_3933788
proquest_miscellaneous_754552300
proquest_miscellaneous_734166000
proquest_journals_1866261964
crossref_primary_10_1002_cne_22239
pubmed_primary_19924828
wiley_primary_10_1002_cne_22239_CNE22239
istex_primary_ark_67375_WNG_3DN9BXHJ_S
PublicationCentury 2000
PublicationDate 15 January 2010
PublicationDateYYYYMMDD 2010-01-15
PublicationDate_xml – month: 01
  year: 2010
  text: 15 January 2010
  day: 15
PublicationDecade 2010
PublicationPlace Hoboken
PublicationPlace_xml – name: Hoboken
– name: United States
– name: New York
PublicationTitle Journal of comparative neurology (1911)
PublicationTitleAlternate J. Comp. Neurol
PublicationYear 2010
Publisher Wiley Subscription Services, Inc., A Wiley Company
Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc., A Wiley Company
– name: Wiley Subscription Services, Inc
References Pixley FJ, Lee PS, Dominguez MG, Einstein DB, Stanley ER. 1995. A heteromorphic protein-tyrosine phosphatase, PTPϕ, is regulated by CSF-1 in macrophages. J Biol Chem 270: 27339-27347.
De Marchis S, Bovetti S, Carletti B, Hsieh YC, Garzotto D, Peretto P, Fasolo A, Puche AC, Rossi F. 2007. Generation of distinct types of periglomerular olfactory bulb interneurons during development and in adult mice: implication for intrinsic properties of the subventricular zone progenitor population. J Neurosci 27: 657-664.
Wharram BL, Goyal M, Gillespie PJ, Wiggins JE, Kershaw DB, Holzman LB, Dysko RC, Saunders TL, Samuelson LC, Wiggins RC. 2000. Altered podocyte structure in GLEPP1 (Ptpro)-deficient mice associated with hypertension and low glomerular filtration rate. J Clin Invest 106: 1281-1290.
Goldshmit Y, McLenachan S, Turnley A. 2006. Roles of Eph receptors and ephrins in the normal and damaged adult CNS. Brain Res Rev 52: 327-345.
Yang DH, Goyal M, Sharif K, Kershaw D, Thomas P, Dysko R, Wiggins R. 1996. Glomerular epithelial protein 1 and podocalyxin-like protein 1 in inflammatory glomerular disease (crescentic nephritis) in rabbit and man. Lab Invest 74: 571-584.
Egger V, Urban NN. 2006. Dynamic connectivity in the mitral cell-granule cell microcircuit. Semin Cell Dev Biol 17: 424-432.
Teng J, Takei Y, Harada A, Nakata T, Chen J, Hirokawa N. 2001. Synergistic effects of MAP2 and MAP1B knockout in neuronal migration, dendritic outgrowth, and microtubule organization. J Cell Biol 155: 65-76.
Inoue E, Deguchi-Tawarada M, Togawa A, Matsui C, Arita K, Katahira-Tayama S, Sato T, Yamauchi E, Oda Y, Takai Y. 2009. Synaptic activity prompts γ-secretase-mediated cleavage of EphA4 and dendritic spine formation. J Cell Biol 185: 551-564.
Stepanek L, Stoker AW, Stoeckli E, Bixby JL. 2005. Receptor tyrosine phosphatases guide vertebrate motor axons during development. J Neurosci 25: 3813-3823.
Whitman MC, Greer CA. 2007a. Adult-generated neurons exhibit diverse developmental fates. Dev Neurobiol 67: 1079-1093.
Huynh DP, Figueroa K, Hoang N, Pulst SM. 2000. Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human. Nat Genet 26: 44-50.
Lamprianou S, Harroch S. 2006. Receptor protein tyrosine phosphatase from stem cells to mature glial cells of the central nervous system. J Mol Neurosci 29: 241-255.
Penzes P, Cahill ME, Jones KA, Srivastava DP. 2008. Convergent CaMK and RacGEF signals control dendritic structure and function. Trends Cell Biol 18: 405-413.
Kosaka K, Toida K, Aika Y, Kosaka T. 1998. How simple is the organization of the olfactory glomerulus? The heterogeneity of so-called periglomerular cells. Neurosci Res 30: 101-110.
Singec I, Knoth R, Ditter M, Hagemeyer CE, Rosenbrock H, Frotscher M, Volk B. 2002. Synaptic vesicle protein synaptoporin is differently expressed by subpopulations of mouse hippocampal neurons. J Comp Neurol 452: 139-153.
Kim JH, Lee JA, Song YM, Park CH, Hwang SJ, Kim YS, Kaang BK, Son H. 2006. Overexpression of calbindin-D28K in hippocampal progenitor cells increases neuronal differentiation and neurite outgrowth. FASEB J 20: 109-111.
Paul S, Lombroso PJ. 2003. Receptor and nonreceptor protein tyrosine phosphatases in the nervous system. Cell Mol Life Sci 60: 2465-2482.
Thomas PE, Wharram BL, Goyal M, Wiggins JE, Holzman LB, Wiggins RC. 1994. GLEPP1, a renal glomerular epithelial cell (podocyte) membrane protein-tyrosine phosphatase. Identification, molecular cloning, and characterization in rabbit. J Biol Chem 269: 19953-19962.
Benzing T. 2004. Signaling at the slit diaphragm. J Am Soc Nephrol 15: 1382-1391.
Binns KL, Taylor PP, Sicheri F, Pawson T, Holland SJ. 2000. Phosphorylation of tyrosine residues in the kinase domain and juxtamembrane region regulates the biological and catalytic activities of Eph receptors. Mol Cell Biol 20: 4791-4805.
Dehmelt L, Halpain S. 2004. Actin and microtubules in neurite initiation: are MAPs the missing link? J Neurobiol 58: 18-33.
Fuentes-Santamaria V, Alvarado JC, Taylor AR, Brunso-Bechtold JK, Henkel CK. 2005. Quantitative changes in calretinin immunostaining in the cochlear nuclei after unilateral cochlear removal in young ferrets. J Comp Neurol 483: 458-475.
Whitman MC, Greer CA. 2007b. Synaptic integration of adult-generated olfactory bulb granule cells: basal axodendritic centrifugal input precedes apical dendrodendritic local circuits. J Neurosci 27: 9951-9961.
Trowern AR, Laight R, MacLean N, Mann DA. 1996. Detection of neuron-specific protein gene product (PGP) 9.5 in the rat and zebrafish using anti-human PGP9.5 antibodies. Neurosci Lett 210: 21-24.
Beltran PJ, Bixby JL, Masters BA. 2003. Expression of PTPRO during mouse development suggests involvement in axonogenesis and differentiation of NT-3- and NGF-dependent neurons. J Comp Neurol 456: 384-395.
Bouvier D, Corera AT, Tremblay ME, Riad M, Chagnon M, Murai KK, Pasquale EB, Fon EA, Doucet G. 2008. Pre-synaptic and post-synaptic localization of EphA4 and EphB2 in adult mouse forebrain. J Neurochem 106: 682-695.
Fong AY, Stornetta RL, Foley CM, Potts JT. 2005. Immunohistochemical localization of GAD67-expressing neurons and processes in the rat brainstem: subregional distribution in the nucleus tractus solitarius. J Comp Neurol 493: 274-290.
Mullen RJ, Buck CR, Smith AM. 1992. NeuN, a neuronal specific nuclear protein in vertebrates. Development 116: 201-211.
Wang R, St John PL, Wiggins RC, Abrahamson DR. 1999. 32 molecular cloning and expression of glomerular epithelial protein 1 (GLEPP1) in developing mouse kidney. J Histochem Cytochem 47: 1650.
Lledo PM, Saghatelyan A. 2005. Integrating new neurons into the adult olfactory bulb: joining the network, life-death decisions, and the effects of sensory experience. Trends Neurosci 28: 248-254.
Faul C, Asanuma K, Yanagida-Asanuma E, Kim K, Mundel P. 2007. Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton. Trends Cell Biol 17: 428-437.
Govek EE, Newey SE, Van Aelst L. 2005. The role of the Rho GTPases in neuronal development. Genes Dev 19: 1-49.
Imamura F, Nagao H, Naritsuka H, Murata Y, Taniguchi H, Mori K. 2006. A leucine-rich repeat membrane protein, 5T4, is expressed by a subtype of granule cells with dendritic arbors in specific strata of the mouse olfactory bulb. J Comp Neurol 495: 754-768.
Parrish-Aungst S, Shipley MT, Erdelyi F, Szabo G, Puche AC. 2007. Quantitative analysis of neuronal diversity in the mouse olfactory bulb. J Comp Neurol 501: 825-836.
Aguiar RC, Yakushijin Y, Kharbanda S, Tiwari S, Freeman GJ, Shipp MA. 1999. PTPROt: an alternatively spliced and developmentally regulated B-lymphoid phosphatase that promotes G0/G1 arrest. Blood 94: 2403-2413.
Duan X, Kang E, Liu CY, Ming GL, Song H. 2008. Development of neural stem cell in the adult brain. Curr Opin Neurobiol 18: 108-115.
Esclapez M, Tillakaratne NJ, Kaufman DL, Tobin AJ, Houser CR. 1994. Comparative localization of two forms of glutamic acid decarboxylase and their mRNAs in rat brain supports the concept of functional differences between the forms. J Neurosci 14: 1834-1855.
Burette AC, Strehler EE, Weinberg RJ. 2009. "Fast" plasma membrane calcium pump PMCA2a concentrates in GABAergic terminals in the adult rat brain. J Comp Neurol 512: 500-513.
Henkemeyer M, Itkis OS, Ngo M, Hickmott PW, Ethell IM. 2003. Multiple EphB receptor tyrosine kinases shape dendritic spines in the hippocampus. J Cell Biol 163: 1313-1326.
Negishi M, Katoh H. 2002. Rho family GTPases as key regulators for neuronal network formation. J Biochem 132: 157-166.
Shintani T, Ihara M, Sakuta H, Takahashi H, Watakabe I, Noda M. 2006. Eph receptors are negatively controlled by protein tyrosine phosphatase receptor type O. Nat Neurosci 9: 761-769.
Hayashi A, Ohnishi H, Okazawa H, Nakazawa S, Ikeda H, Motegi S, Aoki N, Kimura S, Mikuni M, Matozaki T. 2004. Positive regulation of phagocytosis by SIRPβ and its signaling mechanism in macrophages. J Biol Chem 279: 29450-29460.
Wu LW, Baylink DJ, Lau KH. 1996. Molecular cloning and expression of a unique rabbit osteoclastic phosphotyrosyl phosphatase. Biochem J 316: 515-523.
Huot J. 2004. Ephrin signaling in axon guidance. Prog Neuropsychopharmacol Biol Psychiatry 28: 813-818.
Batista-Brito R, Close J, Machold R, Fishell G. 2008. The distinct temporal origins of olfactory bulb interneuron subtypes. J Neurosci 28: 3966-3975.
Shamah SM, Lin MZ, Goldberg JL, Estrach S, Sahin M, Hu L, Bazalakova M, Neve RL, Corfas G, Debant A, Greenberg ME. 2001. EphA receptors regulate growth cone dynamics through the novel guanine nucleotide exchange factor ephexin. Cell 105: 233-244.
Murata T, Ohnishi H, Okazawa H, Murata Y, Kusakari S, Hayashi Y, Miyashita M, Itoh H, Oldenborg PA, Furuya N, Matozaki T. 2006. CD47 promotes neuronal development through Src- and FRG/Vav2-mediated activation of Rac and Cdc42. J Neurosci 26: 12397-12407.
Tomemori T, Seki N, Suzuki Y, Shimizu T, Nagata H, Konno A, Shirasawa T. 2000. Isolation and characterization of murine orthologue of PTP-BK. Biochem Biophys Res Commun 276: 974-981.
Sadakata H, Okazawa H, Sato T, Supriatna Y, Ohnishi H, Kusakari S, Murata Y, Ito T, Nishiyama U, Minegishi T, Harada A, Matozaki T. 2009. SAP-1 is a microvillus-specific protein tyrosine phosphatase that modulates intestinal tumorigenesis. Genes Cells 14: 295-308.
Tagawa M, Shirasawa T, Yahagi Y, Tomoda T, Kuroyanagi H, Fujimura S, Sakiyama S, Maruyama N. 1997. Identification of a receptor-type protein tyrosine phosphatase expressed in postmitotic maturing neurons: its structure and expression in the central nervous system. Biochem J 321: 865-871.
Liebl DJ, Morris CJ, Henkemeyer M, Parada LF. 2003. mRNA expression of ephrins and Eph receptor tyrosine kinases in the neonatal and adult mouse central nervous system. J Neurosci Res 71: 7-22.
Schaapveld RQ, Schepens JT, Bächner D, Attema J, Wieringa B, Jap PH, Hendriks WJ. 1998. Developmental expression of the cell adhesion molecule-like protein tyrosine phosphatases LAR, RPTPδ and
2005; 493
2007; 501
2004; 28
1999; 47
2007a; 67
2006; 495
1996; 74
2008; 106
2005; 28
2007b; 27
1996; 31
2009; 512
2001; 105
2005; 25
2009; 14
2006; 20
1994; 269
2008; 28
2006; 26
1992; 116
2006; 29
1996; 210
1999; 94
2005; 34
2007; 27
2003; 163
2007; 17
2006; 52
2000; 26
2002; 132
2008; 18
2006; 17
2006; 9
2002; 452
2000; 20
2000; 276
2003; 456
2003; 71
2001; 126
1995; 270
2001; 21
2001; 155
2001; 154
2005; 19
2004; 279
2005; 483
2004; 58
1999; 39
2000; 106
2004; 15
1997; 321
1994; 14
2009; 185
1998; 30
2003; 60
2004; 117
1998; 77
1996; 316
1483388 - Development. 1992 Sep;116(1):201-11
12532410 - J Comp Neurol. 2003 Feb 17;456(4):384-95
10973246 - Nat Genet. 2000 Sep;26(1):44-50
16506198 - J Comp Neurol. 2006 Apr 20;495(6):754-68
8910789 - J Neurobiol. 1996 Nov;31(3):309-24
17085782 - J Mol Neurosci. 2006;29(3):241-55
16680165 - Nat Neurosci. 2006 Jun;9(6):761-9
17565001 - Dev Neurobiol. 2007 Jul;67(8):1079-93
15829633 - J Neurosci. 2005 Apr 13;25(15):3813-23
8762182 - Neurosci Lett. 1996 May 24;210(1):21-4
14625689 - Cell Mol Life Sci. 2003 Nov;60(11):2465-82
12478610 - J Neurosci Res. 2003 Jan 1;71(1):7-22
17234597 - J Neurosci. 2007 Jan 17;27(3):657-64
8687395 - Biochem J. 1996 Jun 1;316 ( Pt 2):515-23
16889994 - Semin Cell Dev Biol. 2006 Aug;17(4):424-32
11514594 - J Cell Biol. 2001 Aug 20;154(4):867-78
8126575 - J Neurosci. 1994 Mar;14(3 Pt 2):1834-55
17135401 - J Neurosci. 2006 Nov 29;26(48):12397-407
11172885 - Brain Res Dev Brain Res. 2001 Jan 31;126(1):43-56
19170756 - Genes Cells. 2009 Mar;14(3):295-308
18701290 - Trends Cell Biol. 2008 Sep;18(9):405-13
11336673 - Cell. 2001 Apr 20;105(2):233-44
10848605 - Mol Cell Biol. 2000 Jul;20(13):4791-805
18410519 - J Neurochem. 2008 Jul;106(2):682-95
18514504 - Curr Opin Neurobiol. 2008 Feb;18(1):108-15
15363605 - Prog Neuropsychopharmacol Biol Psychiatry. 2004 Aug;28(5):813-8
7519601 - J Biol Chem. 1994 Aug 5;269(31):19953-62
15866199 - Trends Neurosci. 2005 May;28(5):248-54
7592997 - J Biol Chem. 1995 Nov 10;270(45):27339-47
15700274 - J Comp Neurol. 2005 Mar 21;483(4):458-75
18400896 - J Neurosci. 2008 Apr 9;28(15):3966-75
14598367 - J Neurobiol. 2004 Jan;58(1):18-33
11027578 - Biochem Biophys Res Commun. 2000 Oct 5;276(3):974-81
16278289 - FASEB J. 2006 Jan;20(1):109-11
15123631 - J Biol Chem. 2004 Jul 9;279(28):29450-60
15153549 - J Am Soc Nephrol. 2004 Jun;15(6):1382-91
10567479 - J Histochem Cytochem. 1999 Dec;47(12):1650
15630019 - Genes Dev. 2005 Jan 1;19(1):1-49
17311323 - J Comp Neurol. 2007 Apr 20;501(6):825-36
12271488 - J Comp Neurol. 2002 Oct 14;452(2):139-53
9579643 - Neurosci Res. 1998 Feb;30(2):101-10
8600307 - Lab Invest. 1996 Mar;74(3):571-84
10498613 - Blood. 1999 Oct 1;94(7):2403-13
16841165 - J Neurocytol. 2005 Sep;34(3-5):217-40
19414612 - J Cell Biol. 2009 May 4;185(3):551-64
9032477 - Biochem J. 1997 Feb 1;321 ( Pt 3):865-71
15186772 - Cell. 2004 Jun 11;117(6):699-711
11086029 - J Clin Invest. 2000 Nov;106(10):1281-90
19025983 - J Comp Neurol. 2009 Feb 1;512(4):500-13
11585896 - Mol Cell Biol. 2001 Nov;21(21):7117-36
14691139 - J Cell Biol. 2003 Dec 22;163(6):1313-26
17804239 - Trends Cell Biol. 2007 Sep;17(9):428-37
16255028 - J Comp Neurol. 2005 Dec 12;493(2):274-90
17855609 - J Neurosci. 2007 Sep 12;27(37):9951-61
9784606 - Mech Dev. 1998 Sep;77(1):59-62
16774788 - Brain Res Rev. 2006 Sep;52(2):327-45
10213455 - J Neurobiol. 1999 Apr;39(1):81-96
12153710 - J Biochem. 2002 Aug;132(2):157-66
11581286 - J Cell Biol. 2001 Oct 1;155(1):65-76
e_1_2_6_53_1
e_1_2_6_32_1
e_1_2_6_30_1
Wang R (e_1_2_6_54_1) 1999; 47
e_1_2_6_19_1
e_1_2_6_13_1
e_1_2_6_36_1
e_1_2_6_59_1
e_1_2_6_11_1
e_1_2_6_34_1
e_1_2_6_17_1
e_1_2_6_55_1
e_1_2_6_15_1
e_1_2_6_38_1
e_1_2_6_57_1
e_1_2_6_43_1
e_1_2_6_20_1
e_1_2_6_41_1
Thomas PE (e_1_2_6_51_1) 1994; 269
e_1_2_6_9_1
e_1_2_6_5_1
e_1_2_6_7_1
e_1_2_6_24_1
e_1_2_6_49_1
e_1_2_6_3_1
e_1_2_6_22_1
e_1_2_6_28_1
e_1_2_6_45_1
e_1_2_6_26_1
e_1_2_6_47_1
e_1_2_6_52_1
e_1_2_6_10_1
e_1_2_6_31_1
e_1_2_6_50_1
e_1_2_6_14_1
e_1_2_6_35_1
e_1_2_6_12_1
e_1_2_6_33_1
e_1_2_6_18_1
e_1_2_6_39_1
e_1_2_6_56_1
e_1_2_6_16_1
e_1_2_6_37_1
e_1_2_6_58_1
e_1_2_6_42_1
Yang DH (e_1_2_6_60_1) 1996; 74
e_1_2_6_21_1
e_1_2_6_40_1
e_1_2_6_8_1
e_1_2_6_4_1
e_1_2_6_6_1
Aguiar RC (e_1_2_6_2_1) 1999; 94
e_1_2_6_25_1
e_1_2_6_48_1
e_1_2_6_23_1
e_1_2_6_29_1
e_1_2_6_44_1
e_1_2_6_27_1
e_1_2_6_46_1
References_xml – volume: 28
  start-page: 813
  year: 2004
  end-page: 818
  article-title: Ephrin signaling in axon guidance
  publication-title: Prog Neuropsychopharmacol Biol Psychiatry
– volume: 77
  start-page: 59
  year: 1998
  end-page: 62
  article-title: Developmental expression of the cell adhesion molecule‐like protein tyrosine phosphatases LAR, RPTPδ and RPTPσ in the mouse
  publication-title: Mech Dev
– volume: 52
  start-page: 327
  year: 2006
  end-page: 345
  article-title: Roles of Eph receptors and ephrins in the normal and damaged adult CNS
  publication-title: Brain Res Rev
– volume: 71
  start-page: 7
  year: 2003
  end-page: 22
  article-title: mRNA expression of ephrins and Eph receptor tyrosine kinases in the neonatal and adult mouse central nervous system
  publication-title: J Neurosci Res
– volume: 321
  start-page: 865
  year: 1997
  end-page: 871
  article-title: Identification of a receptor‐type protein tyrosine phosphatase expressed in postmitotic maturing neurons: its structure and expression in the central nervous system
  publication-title: Biochem J
– volume: 116
  start-page: 201
  year: 1992
  end-page: 211
  article-title: NeuN, a neuronal specific nuclear protein in vertebrates
  publication-title: Development
– volume: 27
  start-page: 9951
  year: 2007b
  end-page: 9961
  article-title: Synaptic integration of adult‐generated olfactory bulb granule cells: basal axodendritic centrifugal input precedes apical dendrodendritic local circuits
  publication-title: J Neurosci
– volume: 276
  start-page: 974
  year: 2000
  end-page: 981
  article-title: Isolation and characterization of murine orthologue of PTP‐BK
  publication-title: Biochem Biophys Res Commun
– volume: 47
  start-page: 1650
  year: 1999
  article-title: 32 molecular cloning and expression of glomerular epithelial protein 1 (GLEPP1) in developing mouse kidney
  publication-title: J Histochem Cytochem
– volume: 279
  start-page: 29450
  year: 2004
  end-page: 29460
  article-title: Positive regulation of phagocytosis by SIRPβ and its signaling mechanism in macrophages
  publication-title: J Biol Chem
– volume: 501
  start-page: 825
  year: 2007
  end-page: 836
  article-title: Quantitative analysis of neuronal diversity in the mouse olfactory bulb
  publication-title: J Comp Neurol
– volume: 126
  start-page: 43
  year: 2001
  end-page: 56
  article-title: EphB2 and two of its ligands have dynamic protein expression patterns in the developing olfactory system
  publication-title: Brain Res Dev Brain Res
– volume: 452
  start-page: 139
  year: 2002
  end-page: 153
  article-title: Synaptic vesicle protein synaptoporin is differently expressed by subpopulations of mouse hippocampal neurons
  publication-title: J Comp Neurol
– volume: 163
  start-page: 1313
  year: 2003
  end-page: 1326
  article-title: Multiple EphB receptor tyrosine kinases shape dendritic spines in the hippocampus
  publication-title: J Cell Biol
– volume: 483
  start-page: 458
  year: 2005
  end-page: 475
  article-title: Quantitative changes in calretinin immunostaining in the cochlear nuclei after unilateral cochlear removal in young ferrets
  publication-title: J Comp Neurol
– volume: 15
  start-page: 1382
  year: 2004
  end-page: 1391
  article-title: Signaling at the slit diaphragm
  publication-title: J Am Soc Nephrol
– volume: 132
  start-page: 157
  year: 2002
  end-page: 166
  article-title: Rho family GTPases as key regulators for neuronal network formation
  publication-title: J Biochem
– volume: 106
  start-page: 682
  year: 2008
  end-page: 695
  article-title: Pre‐synaptic and post‐synaptic localization of EphA4 and EphB2 in adult mouse forebrain
  publication-title: J Neurochem
– volume: 512
  start-page: 500
  year: 2009
  end-page: 513
  article-title: “Fast” plasma membrane calcium pump PMCA2a concentrates in GABAergic terminals in the adult rat brain
  publication-title: J Comp Neurol
– volume: 58
  start-page: 18
  year: 2004
  end-page: 33
  article-title: Actin and microtubules in neurite initiation: are MAPs the missing link?
  publication-title: J Neurobiol
– volume: 74
  start-page: 571
  year: 1996
  end-page: 584
  article-title: Glomerular epithelial protein 1 and podocalyxin‐like protein 1 in inflammatory glomerular disease (crescentic nephritis) in rabbit and man
  publication-title: Lab Invest
– volume: 28
  start-page: 3966
  year: 2008
  end-page: 3975
  article-title: The distinct temporal origins of olfactory bulb interneuron subtypes
  publication-title: J Neurosci
– volume: 210
  start-page: 21
  year: 1996
  end-page: 24
  article-title: Detection of neuron‐specific protein gene product (PGP) 9.5 in the rat and zebrafish using anti‐human PGP9.5 antibodies
  publication-title: Neurosci Lett
– volume: 26
  start-page: 12397
  year: 2006
  end-page: 12407
  article-title: CD47 promotes neuronal development through Src‐ and FRG/Vav2‐mediated activation of Rac and Cdc42
  publication-title: J Neurosci
– volume: 106
  start-page: 1281
  year: 2000
  end-page: 1290
  article-title: Altered podocyte structure in GLEPP1 (Ptpro)‐deficient mice associated with hypertension and low glomerular filtration rate
  publication-title: J Clin Invest
– volume: 18
  start-page: 405
  year: 2008
  end-page: 413
  article-title: Convergent CaMK and RacGEF signals control dendritic structure and function
  publication-title: Trends Cell Biol
– volume: 270
  start-page: 27339
  year: 1995
  end-page: 27347
  article-title: A heteromorphic protein‐tyrosine phosphatase, PTPϕ, is regulated by CSF‐1 in macrophages
  publication-title: J Biol Chem
– volume: 9
  start-page: 761
  year: 2006
  end-page: 769
  article-title: Eph receptors are negatively controlled by protein tyrosine phosphatase receptor type O
  publication-title: Nat Neurosci
– volume: 185
  start-page: 551
  year: 2009
  end-page: 564
  article-title: Synaptic activity prompts γ‐secretase‐mediated cleavage of EphA4 and dendritic spine formation
  publication-title: J Cell Biol
– volume: 30
  start-page: 101
  year: 1998
  end-page: 110
  article-title: How simple is the organization of the olfactory glomerulus? The heterogeneity of so‐called periglomerular cells
  publication-title: Neurosci Res
– volume: 60
  start-page: 2465
  year: 2003
  end-page: 2482
  article-title: Receptor and nonreceptor protein tyrosine phosphatases in the nervous system
  publication-title: Cell Mol Life Sci
– volume: 17
  start-page: 428
  year: 2007
  end-page: 437
  article-title: Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton
  publication-title: Trends Cell Biol
– volume: 29
  start-page: 241
  year: 2006
  end-page: 255
  article-title: Receptor protein tyrosine phosphatase from stem cells to mature glial cells of the central nervous system
  publication-title: J Mol Neurosci
– volume: 20
  start-page: 4791
  year: 2000
  end-page: 4805
  article-title: Phosphorylation of tyrosine residues in the kinase domain and juxtamembrane region regulates the biological and catalytic activities of Eph receptors
  publication-title: Mol Cell Biol
– volume: 154
  start-page: 867
  year: 2001
  end-page: 878
  article-title: CRYP‐2/cPTPRO is a neurite inhibitory repulsive guidance cue for retinal neurons in vitro
  publication-title: J Cell Biol
– volume: 31
  start-page: 309
  year: 1996
  end-page: 324
  article-title: CRYP‐2: a receptor‐type tyrosine phosphatase selectively expressed by developing vertebrate neurons
  publication-title: J Neurobiol
– volume: 316
  start-page: 515
  year: 1996
  end-page: 523
  article-title: Molecular cloning and expression of a unique rabbit osteoclastic phosphotyrosyl phosphatase
  publication-title: Biochem J
– volume: 26
  start-page: 44
  year: 2000
  end-page: 50
  article-title: Nuclear localization or inclusion body formation of ataxin‐2 are not necessary for SCA2 pathogenesis in mouse or human
  publication-title: Nat Genet
– volume: 20
  start-page: 109
  year: 2006
  end-page: 111
  article-title: Overexpression of calbindin‐D28K in hippocampal progenitor cells increases neuronal differentiation and neurite outgrowth
  publication-title: FASEB J
– volume: 17
  start-page: 424
  year: 2006
  end-page: 432
  article-title: Dynamic connectivity in the mitral cell–granule cell microcircuit
  publication-title: Semin Cell Dev Biol
– volume: 155
  start-page: 65
  year: 2001
  end-page: 76
  article-title: Synergistic effects of MAP2 and MAP1B knockout in neuronal migration, dendritic outgrowth, and microtubule organization
  publication-title: J Cell Biol
– volume: 94
  start-page: 2403
  year: 1999
  end-page: 2413
  article-title: PTPROt: an alternatively spliced and developmentally regulated B‐lymphoid phosphatase that promotes G0/G1 arrest
  publication-title: Blood
– volume: 67
  start-page: 1079
  year: 2007a
  end-page: 1093
  article-title: Adult‐generated neurons exhibit diverse developmental fates
  publication-title: Dev Neurobiol
– volume: 25
  start-page: 3813
  year: 2005
  end-page: 3823
  article-title: Receptor tyrosine phosphatases guide vertebrate motor axons during development
  publication-title: J Neurosci
– volume: 493
  start-page: 274
  year: 2005
  end-page: 290
  article-title: Immunohistochemical localization of GAD67‐expressing neurons and processes in the rat brainstem: subregional distribution in the nucleus tractus solitarius
  publication-title: J Comp Neurol
– volume: 456
  start-page: 384
  year: 2003
  end-page: 395
  article-title: Expression of PTPRO during mouse development suggests involvement in axonogenesis and differentiation of NT‐3‐ and NGF‐dependent neurons
  publication-title: J Comp Neurol
– volume: 28
  start-page: 248
  year: 2005
  end-page: 254
  article-title: Integrating new neurons into the adult olfactory bulb: joining the network, life‐death decisions, and the effects of sensory experience
  publication-title: Trends Neurosci
– volume: 269
  start-page: 19953
  year: 1994
  end-page: 19962
  article-title: GLEPP1, a renal glomerular epithelial cell (podocyte) membrane protein‐tyrosine phosphatase. Identification, molecular cloning, and characterization in rabbit
  publication-title: J Biol Chem
– volume: 19
  start-page: 1
  year: 2005
  end-page: 49
  article-title: The role of the Rho GTPases in neuronal development
  publication-title: Genes Dev
– volume: 14
  start-page: 1834
  year: 1994
  end-page: 1855
  article-title: Comparative localization of two forms of glutamic acid decarboxylase and their mRNAs in rat brain supports the concept of functional differences between the forms
  publication-title: J Neurosci
– volume: 495
  start-page: 754
  year: 2006
  end-page: 768
  article-title: A leucine‐rich repeat membrane protein, 5T4, is expressed by a subtype of granule cells with dendritic arbors in specific strata of the mouse olfactory bulb
  publication-title: J Comp Neurol
– volume: 27
  start-page: 657
  year: 2007
  end-page: 664
  article-title: Generation of distinct types of periglomerular olfactory bulb interneurons during development and in adult mice: implication for intrinsic properties of the subventricular zone progenitor population
  publication-title: J Neurosci
– volume: 14
  start-page: 295
  year: 2009
  end-page: 308
  article-title: SAP‐1 is a microvillus‐specific protein tyrosine phosphatase that modulates intestinal tumorigenesis
  publication-title: Genes Cells
– volume: 105
  start-page: 233
  year: 2001
  end-page: 244
  article-title: EphA receptors regulate growth cone dynamics through the novel guanine nucleotide exchange factor ephexin
  publication-title: Cell
– volume: 34
  start-page: 217
  year: 2005
  end-page: 240
  article-title: Olfactory epithelia differentially express neuronal markers
  publication-title: J Neurocytol
– volume: 21
  start-page: 7117
  year: 2001
  end-page: 7136
  article-title: Structural and evolutionary relationships among protein tyrosine phosphatase domains
  publication-title: Mol Cell Biol
– volume: 18
  start-page: 108
  year: 2008
  end-page: 115
  article-title: Development of neural stem cell in the adult brain
  publication-title: Curr Opin Neurobiol
– volume: 39
  start-page: 81
  year: 1999
  end-page: 96
  article-title: Expression of receptor tyrosine phosphatases during development of the retinotectal projection of the chick
  publication-title: J Neurobiol
– volume: 117
  start-page: 699
  year: 2004
  end-page: 711
  article-title: Protein tyrosine phosphatases in the human genome
  publication-title: Cell
– ident: e_1_2_6_24_1
  doi: 10.1016/j.pnpbp.2004.05.025
– ident: e_1_2_6_44_1
  doi: 10.1038/nn1697
– ident: e_1_2_6_16_1
  doi: 10.1523/JNEUROSCI.14-03-01834.1994
– ident: e_1_2_6_38_1
  doi: 10.1007/s00018-003-3123-7
– ident: e_1_2_6_48_1
  doi: 10.1523/JNEUROSCI.4531-04.2005
– ident: e_1_2_6_35_1
  doi: 10.1523/JNEUROSCI.3981-06.2006
– ident: e_1_2_6_28_1
  doi: 10.1096/fj.05-4826fje
– ident: e_1_2_6_42_1
  doi: 10.1016/S0925-4773(98)00119-1
– ident: e_1_2_6_50_1
  doi: 10.1083/jcb.200106025
– ident: e_1_2_6_23_1
  doi: 10.1083/jcb.200306033
– ident: e_1_2_6_29_1
  doi: 10.1016/S0168-0102(98)00002-9
– ident: e_1_2_6_25_1
  doi: 10.1038/79162
– ident: e_1_2_6_52_1
  doi: 10.1006/bbrc.2000.3584
– ident: e_1_2_6_33_1
  doi: 10.1016/j.tins.2005.03.005
– ident: e_1_2_6_13_1
  doi: 10.1002/neu.10284
– ident: e_1_2_6_4_1
  doi: 10.1128/MCB.21.21.7117-7136.2001
– ident: e_1_2_6_15_1
  doi: 10.1016/j.semcdb.2006.04.006
– ident: e_1_2_6_31_1
  doi: 10.1002/(SICI)1097-4695(199904)39:1<81::AID-NEU7>3.0.CO;2-K
– volume: 74
  start-page: 571
  year: 1996
  ident: e_1_2_6_60_1
  article-title: Glomerular epithelial protein 1 and podocalyxin‐like protein 1 in inflammatory glomerular disease (crescentic nephritis) in rabbit and man
  publication-title: Lab Invest
  contributor:
    fullname: Yang DH
– ident: e_1_2_6_21_1
  doi: 10.1101/gad.1256405
– ident: e_1_2_6_10_1
  doi: 10.1111/j.1471-4159.2008.05416.x
– ident: e_1_2_6_11_1
  doi: 10.1002/cne.21909
– ident: e_1_2_6_19_1
  doi: 10.1002/cne.20437
– ident: e_1_2_6_26_1
  doi: 10.1002/cne.20896
– ident: e_1_2_6_41_1
  doi: 10.1111/j.1365-2443.2008.01270.x
– ident: e_1_2_6_39_1
  doi: 10.1016/j.tcb.2008.07.002
– volume: 47
  start-page: 1650
  year: 1999
  ident: e_1_2_6_54_1
  article-title: 32 molecular cloning and expression of glomerular epithelial protein 1 (GLEPP1) in developing mouse kidney
  publication-title: J Histochem Cytochem
  contributor:
    fullname: Wang R
– ident: e_1_2_6_7_1
  doi: 10.1097/01.ASN.0000130167.30769.55
– ident: e_1_2_6_27_1
  doi: 10.1083/jcb.200809151
– ident: e_1_2_6_55_1
  doi: 10.1007/s11068-005-8355-z
– ident: e_1_2_6_18_1
  doi: 10.1002/cne.20758
– ident: e_1_2_6_3_1
  doi: 10.1016/j.cell.2004.05.018
– ident: e_1_2_6_32_1
  doi: 10.1002/jnr.10457
– ident: e_1_2_6_59_1
  doi: 10.1042/bj3160515
– ident: e_1_2_6_22_1
  doi: 10.1074/jbc.M400950200
– ident: e_1_2_6_30_1
  doi: 10.1385/JMN:29:3:241
– ident: e_1_2_6_47_1
  doi: 10.1083/jcb.200105019
– ident: e_1_2_6_8_1
  doi: 10.1128/MCB.20.13.4791-4805.2000
– volume: 269
  start-page: 19953
  year: 1994
  ident: e_1_2_6_51_1
  article-title: GLEPP1, a renal glomerular epithelial cell (podocyte) membrane protein‐tyrosine phosphatase. Identification, molecular cloning, and characterization in rabbit
  publication-title: J Biol Chem
  doi: 10.1016/S0021-9258(17)32113-0
  contributor:
    fullname: Thomas PE
– ident: e_1_2_6_49_1
  doi: 10.1042/bj3210865
– ident: e_1_2_6_58_1
  doi: 10.1523/JNEUROSCI.1633-07.2007
– ident: e_1_2_6_5_1
  doi: 10.1523/JNEUROSCI.5625-07.2008
– ident: e_1_2_6_12_1
  doi: 10.1523/JNEUROSCI.2870-06.2007
– ident: e_1_2_6_6_1
  doi: 10.1002/cne.10532
– ident: e_1_2_6_20_1
  doi: 10.1016/j.brainresrev.2006.04.006
– ident: e_1_2_6_14_1
  doi: 10.1016/j.conb.2008.04.001
– ident: e_1_2_6_56_1
  doi: 10.1172/JCI7236
– ident: e_1_2_6_36_1
  doi: 10.1093/oxfordjournals.jbchem.a003205
– ident: e_1_2_6_46_1
  doi: 10.1016/S0165-3806(00)00136-X
– ident: e_1_2_6_34_1
  doi: 10.1242/dev.116.1.201
– ident: e_1_2_6_17_1
  doi: 10.1016/j.tcb.2007.06.006
– volume: 94
  start-page: 2403
  year: 1999
  ident: e_1_2_6_2_1
  article-title: PTPROt: an alternatively spliced and developmentally regulated B‐lymphoid phosphatase that promotes G0/G1 arrest
  publication-title: Blood
  doi: 10.1182/blood.V94.7.2403.419k39_2403_2413
  contributor:
    fullname: Aguiar RC
– ident: e_1_2_6_45_1
  doi: 10.1002/cne.10371
– ident: e_1_2_6_43_1
  doi: 10.1016/S0092-8674(01)00314-2
– ident: e_1_2_6_57_1
  doi: 10.1002/dneu.20389
– ident: e_1_2_6_37_1
  doi: 10.1002/cne.21205
– ident: e_1_2_6_9_1
  doi: 10.1002/(SICI)1097-4695(199611)31:3<309::AID-NEU4>3.0.CO;2-E
– ident: e_1_2_6_40_1
  doi: 10.1074/jbc.270.45.27339
– ident: e_1_2_6_53_1
  doi: 10.1016/0304-3940(96)12640-9
SSID ssj0009938
Score 2.083472
Snippet PTPRO is a receptor‐type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III‐like...
PTPRO is a receptor-type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type III-like...
Abstract PTPRO is a receptor‐type protein tyrosine phosphatase (PTP) with a single catalytic domain in its cytoplasmic region and multiple fibronectin type...
SourceID pubmedcentral
proquest
crossref
pubmed
wiley
istex
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 119
SubjectTerms Animals
Antibodies, Monoclonal - chemistry
Biomarkers
Cells, Cultured
CNS
Female
Fluorescent Antibody Technique
gamma-Aminobutyric Acid - metabolism
granule cells
Indicators and Reagents
Interneurons - metabolism
localization
Male
maturation
Mice
Mice, Inbred C57BL
Olfactory Bulb - cytology
Olfactory Bulb - metabolism
periglomerular cells
Plasmids - genetics
Pregnancy
Receptor, EphA4 - metabolism
Receptor-Like Protein Tyrosine Phosphatases, Class 3 - biosynthesis
Receptor-Like Protein Tyrosine Phosphatases, Class 3 - genetics
Receptor-Like Protein Tyrosine Phosphatases, Class 3 - isolation & purification
receptor-type tyrosine phosphatase
Transfection
Title Expression of PTPRO in the interneurons of adult mouse olfactory bulb
URI https://api.istex.fr/ark:/67375/WNG-3DN9BXHJ-S/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcne.22239
https://www.ncbi.nlm.nih.gov/pubmed/19924828
https://www.proquest.com/docview/1866261964
https://search.proquest.com/docview/734166000
https://search.proquest.com/docview/754552300
https://pubmed.ncbi.nlm.nih.gov/PMC3933788
Volume 518
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3daxQxEB9KRfDF74_VKkFEfNnrZrNJNvik7dWj4Flqi4cIIclm8WjZk94dVP96M9nbPc8vxLeFTGAzmcn8Mpn8AvBMZqrKilqknss6LbhkqcmcSCtqKu9sCNkWT3TfjsXotDic8MkWvOzuwrT8EH3CDT0jrtfo4MbOd9ekoa7xAwxueHmPMonlXPvHa-qoEHfbVRhLEJSQHatQlu_2PTdi0RVU6-XvgOav9ZI_4tgYiA5uwKduCG39ydlgubAD9-0ndsf_HONNuL4CqORVa1G3YMs3t-Hqx1lMv9-B4fByVTrbkFlNjk6Ojt-RaUMCjiTTmF1Eto9mjo2R24NgbsGT2Xn7ss9XYpfn9i6cHgxP9kbp6imG1AWXVml8Zb3GCws889RLWgmeW1tyUZbcUGmUYVXOSyclK3zYYjoToIasPaudC8sCuwfbzazxD4BkNTU-t1XoIwpVCVVIz1nmjOAVLVWVwNNuUvSXlnFDt9zKuQ760FEfCTyP09VLmIszLFGTXH8Yv9Fsf6xeT0aH-n0CO9186pV3zjWS_OHOURQJkL45-BUelpjGB73oMA4qAhrM_iIS0Ccm1YPI_dZA1j-swr42bGYTkBum0wsgq_dmSzP9HNm9mWLI8Z_Ai2gZf9aB3hsP48fDfxd9BNfa8geaUr4D24uLpX8cUNXCPonu8x06qxx4
link.rule.ids 230,315,783,787,888,1378,27937,27938,46307,46731
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwED-NTYi98A0LDLAQQrykS-LYjiVeYOsoYwvT6LQKCVmO44hqU4q2Vhr89ficJqV8CfEWyWcpPt_Pdz6ffwZ4JiJZRmnFQ8tEFaZM0FBHhodlrEtrCueyCzzRPcj54DjdG7HRCrxs78I0_BBdwg2R4ddrBDgmpLcWrKGmtj30bvIKrDm4U4TlztGCPMp53mYdxiIEyUXLKxQlW13XJW-0hoq9_F2o-WvF5I-RrHdFuzfgUzuIpgLltDebFj3z7Sd-x_8d5U24Po9RyavGqG7Biq1vw9WPE5-BvwP9_uW8erYmk4ocDg-P3pNxTVwoScY-wYiEH_UFNnp6D4LpBUsmZ83jPl9JMTsr7sLxbn-4PQjnrzGExqFahv6h9QrvLLDIxlbEJWdJUWSMZxnTsdBS0zJhmRGCptbtMo120YaoLK2McSsDvQer9aS2G0CiKtY2KUrXh6ey5DIVltHIaM7KOJNlAE_bWVFfGtIN1dArJ8rpQ3l9BPDcz1cnoc9PsUpNMHWSv1F0J5evR4M99SGAzXZC1RygFwp5_nDzyNMASNfsoIXnJbq2Ti_KjSPmLiCM_iLiAlDMqzuR-42FLH5Yuq2t288GIJZspxNAYu_llnr82RN8U0mR5j-AF940_qwDtZ33_ceDfxd9AtcGw4N9tf82f_cQ1ptqiDiM2SasTs9n9pELsqbFY4-l7-SAIJE
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3daxQxEB9qi-KL39rVqkFEfNnrfiXZ4JO2d55V16O2eIgQskmWHi17pb2D6l_vJHu75_mF-LaQCWwmM5lfJpNfAJ7ySJgoq1hoKa_CjPI0VJFmoYmVsbrEkF26E933BRseZntjOl6DF-1dmIYfoku4Oc_w67Vz8FNTbS9JQ3Vtey64iUuwkTE0VYeI9pfcURh4m2XY1SAIxltaoSjZ7rquBKMNp9eL3yHNXwsmfwSyPhINrsOXdgxNAcpxbz4re_rbT_SO_znIG3BtgVDJy8akbsKarW_B5c9Tn3-_Df3-xaJ2tibTiowORvsfyKQmCCTJxKcXHd1Hfe4aPbkHcckFS6YnzdM-X0k5PynvwOGgf7AzDBdvMYQafVqE_pn1yt1YoJGNLY8No0lZ5pTlOVUxV0KlJqG55jzNLO4xtUKswSubVlrjupDehfV6WttNIFEVK5uUBvuwTBgmMm5pGmnFqIlzYQJ40k6KPG0oN2RDrpxI1If0-gjgmZ-uTkKdHbsaNU7lp-K1THcL8Wo83JMfA9hq51Mu3PNcOpY_t3VkWQCka0bHcqclqraoF4njiBnCwegvIgg_XVYdRe41BrL8YYEbW9zNBsBXTKcTcLTeqy315MjTe6cidST_ATz3lvFnHcidou8_7v-76GO4MtodyHdvircP4GpTChGHMd2C9dnZ3D5EhDUrH3lP-g5six9A
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Expression+of+PTPRO+in+the+interneurons+of+adult+mouse+olfactory+bulb&rft.jtitle=Journal+of+comparative+neurology+%281911%29&rft.au=Kotani%2C+Takenori&rft.au=Murata%2C+Yoji&rft.au=Ohnishi%2C+Hiroshi&rft.au=Mori%2C+Munemasa&rft.date=2010-01-15&rft.eissn=1096-9861&rft.volume=518&rft.issue=2&rft.spage=119&rft_id=info:doi/10.1002%2Fcne.22239&rft_id=info%3Apmid%2F19924828&rft.externalDocID=19924828
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0021-9967&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0021-9967&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0021-9967&client=summon