Quantitative trait loci affecting the behavior of A/J and CBA/J intercross mice in the elevated plus maze

How allelic diversity affects neural mechanisms to produce behavioral variation is largely unknown. The elevated plus maze, consisting of open and closed arms, has been used as a model of behavioral variation in rodent exploration. Under dim illumination the nature of the sensory stimuli that influe...

Full description

Saved in:
Bibliographic Details
Published inMammalian genome Vol. 12; no. 7; pp. 501 - 507
Main Authors Cohen, R M, Kang, A, Gulick, C
Format Journal Article
LanguageEnglish
Published United States Springer Nature B.V 01.07.2001
Subjects
Online AccessGet full text

Cover

Loading…
Abstract How allelic diversity affects neural mechanisms to produce behavioral variation is largely unknown. The elevated plus maze, consisting of open and closed arms, has been used as a model of behavioral variation in rodent exploration. Under dim illumination the nature of the sensory stimuli that influence arm choice is uncertain. Two inbred mouse strains, A/J (Tyrc/Tyrc, the albino phenotype, mutation in tyrosinase) with a strong preference for closed arm entry, and CBA/J (Pdebrdl/Pdebrdl, the retinal degeneration phenotype, mutation in the beta-subunit of rod cGMP phosphodiesterase), with a weak preference for open arm entry, were studied under varying light. Because behavioral differences persist under red light, variation in light perception is not likely to fully account for variation in arm choice. To identify genetic factors influencing arm choice (100 x Open arm entries/Total arm entries) quantitative trait loci analyses (QTL) were performed on (A/J x CBA/J)F2 mice. Two QTLs, one of which includes PDEB, were identified on Chr 5 (LOD > 10) and account for > 30% of the behavioral variation in arm preference. Tyr (Chr 7, 44 cM) was linked to closed arm entries but not arm preference, and is unlikely to be acting through a direct effect on light perception, because A/J arm entries were not affected by red light and there was no interaction with PDEB in the (A/J x CBA/J)F2 mice. Whether the candidate QTLs on Chr 5 affect arm choice through an effect on light perception is unknown, but phenotypic differences between F2 mice with retinal degeneration and CBA/J mice and F2 mice with albinism and A/J mice suggest that factors other than light sensitivity contribute to arm preference in these two strains.
AbstractList How allelic diversity affects neural mechanisms to produce behavioral variation is largely unknown. The elevated plus maze, consisting of open and closed arms, has been used as a model of behavioral variation in rodent exploration. Under dim illumination the nature of the sensory stimuli that influence arm choice is uncertain. Two inbred mouse strains, A/J (Tyrc/Tyrc, the albino phenotype, mutation in tyrosinase) with a strong preference for closed arm entry, and CBA/J (Pdebrdl/Pdebrdl, the retinal degeneration phenotype, mutation in the beta-subunit of rod cGMP phosphodiesterase), with a weak preference for open arm entry, were studied under varying light. Because behavioral differences persist under red light, variation in light perception is not likely to fully account for variation in arm choice. To identify genetic factors influencing arm choice (100 x Open arm entries/Total arm entries) quantitative trait loci analyses (QTL) were performed on (A/J x CBA/J)F2 mice. Two QTLs, one of which includes PDEB, were identified on Chr 5 (LOD > 10) and account for > 30% of the behavioral variation in arm preference. Tyr (Chr 7, 44 cM) was linked to closed arm entries but not arm preference, and is unlikely to be acting through a direct effect on light perception, because A/J arm entries were not affected by red light and there was no interaction with PDEB in the (A/J x CBA/J)F2 mice. Whether the candidate QTLs on Chr 5 affect arm choice through an effect on light perception is unknown, but phenotypic differences between F2 mice with retinal degeneration and CBA/J mice and F2 mice with albinism and A/J mice suggest that factors other than light sensitivity contribute to arm preference in these two strains.
How allelic diversity affects neural mechanisms to produce behavioral variation is largely unknown. The elevated plus maze, consisting of open and closed arms, has been used as a model of behavioral variation in rodent exploration. Under dim illumination the nature of the sensory stimuli that influence arm choice is uncertain. Two inbred mouse strains, A/J (Tyr^sup c^ /Tyr^sup c^ , the albino phenotype, mutation in tyrosinase) with a strong preference for closed arm entry, and CBA/J (Pdeb^sup rdl^ /Pdeb^sup rdl^ , the retinal degeneration phenotype, mutation in the β-subunit of rod cGMP phosphodiesterase), with a weak preference for open arm entry, were studied under varying light. Because behavioral differences persist under red light, variation in light perception is not likely to fully account for variation in arm choice. To identify genetic factors influencing arm choice (100 × Open arm entries/Total arm entries) quantitative trait loci analyses (QTL) were performed on (A/J × CBA/J)F^sub 2^ mice. Two QTLs, one of which includes PDEB, were identified on Chr 5 (LOD > 10) and account for > 30% of the behavioral variation in arm preference. Tyr (Chr 7, 44 cM) was linked to closed arm entries but not arm preference, and is unlikely to be acting through a direct effect on light perception, because A/J arm entries were not affected by red light and there was no interaction with PDEB in the (A/J × CBA/J)F^sub 2^ mice. Whether the candidate QTLs on Chr 5 affect arm choice through an effect on light perception is unknown, but phenotypic differences between F^sub 2^ mice with retinal degeneration and CBA/J mice and F^sub 2^ mice with albinism and A/J mice suggest that factors other than light sensitivity contribute to arm preference in these two strains.[PUBLICATION ABSTRACT]
How allelic diversity affects neural mechanisms to produce behavioral variation is largely unknown. The elevated plus maze, consisting of open and closed arms, has been used as a model of behavioral variation in rodent exploration. Under dim illumination the nature of the sensory stimuli that influence arm choice is uncertain. Two inbred mouse strains, A/J (Tyr super(c)/Tyr super(c), the albino phenotype, mutation in tyrosinase) with a strong preference for closed arm entry, and CBA/J (Pdeb super(rdl)/Pdeb super(rdl), the retinal degeneration phenotype, mutation in the beta -subunit of rod cGMP phosphodiesterase), with a weak preference for open arm entry, were studied under varying light. Because behavioral differences persist under red light, variation in light perception is not likely to fully account for variation in arm choice. To identify genetic factors influencing arm choice (100 Open arm entries/Total arm entries) quantitative trait loci analyses (QTL) were performed on (A/J CBA/J)F2 mice. Two QTLs, one of which includes PDEB, were identified on Chr 5 (LOD 10) and account for 30% of the behavioral variation in arm preference. Tyr (Chr 7, 44 cM) was linked to closed arm entries but not arm preference, and is unlikely to be acting through a direct effect on light perception, because A/J arm entries were not affected by red light and there was no interaction with PDEB in the (A/J CBA/J)F2 mice. Whether the candidate QTLs on Chr 5 affect arm choice through an effect on light perception is unknown, but phenotypic differences between F2 mice with retinal degeneration and CBA/J mice and F2 mice with albinism and A/J mice suggest that factors other than light sensitivity contribute to arm preference in these two strains.
Author Kang, A
Gulick, C
Cohen, R M
Author_xml – sequence: 1
  givenname: R M
  surname: Cohen
  fullname: Cohen, R M
  email: bob@shiloh.nimh.nih.gov
  organization: Laboratory of Cerebral Metabolism and Geriatric Psychiatry Branch, National Institute of Mental Health, NIH, Bldg. 10, Room 3N218, 10 Center Dr. MSC 1274, Bethesda, Maryland, 20892-1274, USA. bob@shiloh.nimh.nih.gov
– sequence: 2
  givenname: A
  surname: Kang
  fullname: Kang, A
– sequence: 3
  givenname: C
  surname: Gulick
  fullname: Gulick, C
BackLink https://www.ncbi.nlm.nih.gov/pubmed/11420611$$D View this record in MEDLINE/PubMed
BookMark eNqFkUtLJDEQgMOirKO7P8DLEljw1lp5dKf76A4-EUTQc6hJV2ukp3s2SQ_orzfjDCzsxVMq1FdFVX2HbG8YB2LsWMCpADBnEUCpsgAQhQRtivIbmwmtZCGMMXtsBo2qi7pp4IAdxviaOVMJ850dCKElVELMmH-YcEg-YfJr4imgT7wfnefYdeSSH555eiG-oBdc-zHwsePnZ7cch5bP_2wiPyQKLowx8qV3lP-fBdTTGhO1fNVPOYPv9IPtd9hH-rl7j9jT5cXj_Lq4u7-6mZ_fFU6VVSoIZSXrduEWQGWrHJVNg7VrtdEKAKraoKtL0LIDraUhZUg3iJ1UlJNYqyN2su27CuPfiWKySx8d9T0ONE7RGmiMlGX5JShMPp2uZAZ__we-jlMY8hJWgBRG5YlNpsSW-jxGoM6ugl9ieMuQ3eiyW102a7AbXXYzwq9d52mxpPZfxc6P-gAE65AN
CitedBy_id crossref_primary_10_1016_S0014_5793_02_03190_3
crossref_primary_10_1186_1752_0509_5_43
crossref_primary_10_1086_342900
crossref_primary_10_1124_jpet_302_1_145
crossref_primary_10_1146_annurev_neuro_27_070203_144212
crossref_primary_10_1111_gbb_12825
crossref_primary_10_1016_j_bbr_2005_01_013
crossref_primary_10_1016_S1673_8527_08_60020_X
crossref_primary_10_1016_j_pbb_2021_173312
crossref_primary_10_1111_j_1601_183X_2006_00295_x
crossref_primary_10_1093_cercor_bhy297
crossref_primary_10_1111_j_1601_183X_2009_00516_x
crossref_primary_10_1007_s00265_021_03003_6
crossref_primary_10_1007_s10519_008_9203_6
crossref_primary_10_1111_j_1601_183X_2004_00071_x
crossref_primary_10_1017_S1461145709990447
crossref_primary_10_1038_s41598_022_13127_y
crossref_primary_10_1038_ng1840
crossref_primary_10_1016_j_bbr_2010_02_029
crossref_primary_10_1093_hmg_ddm277
crossref_primary_10_1002_prp2_223
crossref_primary_10_1038_sj_ejhg_5201569
crossref_primary_10_1016_j_peptides_2004_01_008
crossref_primary_10_1002_neu_10161
ContentType Journal Article
Copyright Springer-Verlag New York Inc. 2001
Copyright_xml – notice: Springer-Verlag New York Inc. 2001
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
3V.
7TK
7X7
7XB
88A
88E
8AO
8FD
8FE
8FH
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
FR3
FYUFA
GHDGH
GNUQQ
HCIFZ
K9.
LK8
M0S
M1P
M7P
P64
PQEST
PQQKQ
PQUKI
RC3
7X8
DOI 10.1007/s00335-001-2047-5
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
ProQuest Central (Corporate)
Neurosciences Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Biology Database (Alumni Edition)
Medical Database (Alumni Edition)
ProQuest Pharma Collection
Technology Research Database
ProQuest SciTech Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central Korea
Engineering Research Database
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
SciTech Premium Collection (Proquest) (PQ_SDU_P3)
ProQuest Health & Medical Complete (Alumni)
ProQuest Biological Science Collection
Health & Medical Collection (Alumni Edition)
Medical Database
Biological Science Database
Biotechnology and BioEngineering Abstracts
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
Genetics Abstracts
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
ProQuest Central Student
Technology Research Database
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Biology Journals (Alumni Edition)
ProQuest Central
Genetics Abstracts
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Biological Science Collection
ProQuest Medical Library (Alumni)
ProQuest Biological Science Collection
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
Neurosciences Abstracts
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Engineering Research Database
ProQuest One Academic
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE
ProQuest Central Student
Genetics 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
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Zoology
EISSN 1432-1777
EndPage 507
ExternalDocumentID 2693847271
10_1007_s00335_001_2047_5
11420611
Genre Journal Article
GroupedDBID ---
-4W
-56
-5G
-BR
-EM
-Y2
-~C
-~X
.86
.GJ
.VR
06C
06D
0R~
0VY
199
1N0
1SB
2.D
203
28-
29M
29~
2J2
2JN
2JY
2KG
2KM
2LR
2P1
2VQ
2~H
30V
36B
3SX
3V.
4.4
406
408
409
40D
40E
53G
5GY
5QI
5VS
67N
67Z
6NX
78A
7X7
88A
88E
8AO
8FE
8FH
8FI
8FJ
8TC
8UJ
95-
95.
95~
96X
AAAVM
AABHQ
AACDK
AAEOY
AAHBH
AAHNG
AAIAL
AAJBT
AAJKR
AANXM
AANZL
AAQLM
AARHV
AARTL
AASML
AATNV
AATVU
AAUYE
AAWCG
AAYIU
AAYQN
AAYTO
AAYZH
ABAKF
ABBBX
ABBXA
ABDBF
ABDZT
ABECU
ABFTV
ABHLI
ABHQN
ABJNI
ABJOX
ABKCH
ABKTR
ABMNI
ABMQK
ABNWP
ABPLI
ABQBU
ABSXP
ABTEG
ABTHY
ABTKH
ABTMW
ABULA
ABUWG
ABWNU
ABXPI
ACAOD
ACBXY
ACDTI
ACGFS
ACHSB
ACHXU
ACIPQ
ACKNC
ACMDZ
ACMLO
ACOKC
ACOMO
ACPRK
ACZOJ
ADBBV
ADHHG
ADHIR
ADIMF
ADINQ
ADKNI
ADKPE
ADRFC
ADTPH
ADURQ
ADYFF
ADYPR
ADZKW
AEBTG
AEFIE
AEFQL
AEGAL
AEGNC
AEJHL
AEJRE
AEKMD
AEMSY
AENEX
AEOHA
AEPYU
AESKC
AETLH
AEVLU
AEXYK
AFBBN
AFEXP
AFFNX
AFGCZ
AFKRA
AFLOW
AFQWF
AFWTZ
AFZKB
AGAYW
AGDGC
AGGDS
AGJBK
AGMZJ
AGQEE
AGQMX
AGRTI
AGWIL
AGWZB
AGYKE
AHAVH
AHBYD
AHKAY
AHMBA
AHSBF
AHYZX
AIAKS
AIGIU
AIIXL
AILAN
AITGF
AJBLW
AJRNO
AJZVZ
AKMHD
ALIPV
ALMA_UNASSIGNED_HOLDINGS
ALWAN
AMKLP
AMXSW
AMYLF
AMYQR
AOCGG
ARMRJ
ASPBG
AVWKF
AXYYD
AZFZN
B-.
B0M
BA0
BBNVY
BBWZM
BDATZ
BENPR
BGNMA
BHPHI
BPHCQ
BVXVI
CAG
CCPQU
CGR
COF
CS3
CSCUP
CUY
CVF
DDRTE
DL5
DNIVK
DPUIP
DU5
EAD
EAP
EBD
EBLON
EBS
ECM
EIF
EIOEI
EJD
EMB
EMK
EMOBN
EN4
EPAXT
EPL
ESBYG
ESX
F5P
FEDTE
FERAY
FFXSO
FIGPU
FINBP
FNLPD
FRRFC
FSGXE
FWDCC
FYUFA
G-Y
G-Z
GGCAI
GGRSB
GJIRD
GNWQR
GQ6
GQ7
GQ8
GXS
H13
HCIFZ
HF~
HG5
HG6
HMCUK
HMJXF
HQYDN
HRMNR
HVGLF
HZ~
I09
IHE
IJ-
IKXTQ
ITM
IWAJR
IXC
IZIGR
IZQ
I~X
I~Z
J-C
J0Z
JBSCW
JCJTX
JZLTJ
KDC
KOV
KOW
KPH
LAS
LK8
LLZTM
M0L
M1P
M4Y
M7P
MA-
N2Q
NB0
NDZJH
NPM
NPVJJ
NQJWS
NU0
O9-
O93
O9G
O9I
O9J
OAM
OVD
P19
P2P
PF0
PQQKQ
PROAC
PSQYO
PT4
PT5
Q2X
QOK
QOR
QOS
R4E
R89
R9I
RHV
RIG
RNI
ROL
RPX
RRX
RSV
RZK
S16
S1Z
S26
S27
S28
S3A
S3B
SAP
SBL
SBY
SCLPG
SDH
SDM
SHX
SISQX
SJYHP
SNE
SNPRN
SNX
SOHCF
SOJ
SPISZ
SRMVM
SSLCW
SSXJD
STPWE
SV3
SZN
T13
T16
TEORI
TN5
TSG
TSK
TSV
TUC
TUS
U2A
U9L
UG4
UKHRP
UOJIU
UTJUX
UZXMN
VC2
VFIZW
W23
W48
WJK
WK6
WK8
YLTOR
Z45
Z7U
Z82
Z87
Z8O
Z8V
Z91
ZGI
ZMTXR
ZOVNA
ZXP
~8M
~A9
~EX
~KM
AAYXX
CITATION
7TK
7XB
8FD
8FK
AZQEC
DWQXO
FR3
GNUQQ
K9.
P64
PQEST
PQUKI
RC3
7X8
ID FETCH-LOGICAL-c356t-ea2628dbcb0e5d3ce599a8cd4743000687ac85042f04427e37e49aaf23e068a83
IEDL.DBID 7X7
ISSN 0938-8990
IngestDate Fri Oct 25 00:01:56 EDT 2024
Fri Oct 25 22:07:29 EDT 2024
Thu Oct 10 22:12:32 EDT 2024
Thu Sep 12 18:12:25 EDT 2024
Wed Oct 16 00:53:26 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 7
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c356t-ea2628dbcb0e5d3ce599a8cd4743000687ac85042f04427e37e49aaf23e068a83
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
PMID 11420611
PQID 1021732627
PQPubID 54093
PageCount 7
ParticipantIDs proquest_miscellaneous_70972255
proquest_miscellaneous_17899462
proquest_journals_1021732627
crossref_primary_10_1007_s00335_001_2047_5
pubmed_primary_11420611
PublicationCentury 2000
PublicationDate 2001-07-01
PublicationDateYYYYMMDD 2001-07-01
PublicationDate_xml – month: 07
  year: 2001
  text: 2001-07-01
  day: 01
PublicationDecade 2000
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: New York
PublicationTitle Mammalian genome
PublicationTitleAlternate Mamm Genome
PublicationYear 2001
Publisher Springer Nature B.V
Publisher_xml – name: Springer Nature B.V
SSID ssj0017617
Score 1.7808249
Snippet How allelic diversity affects neural mechanisms to produce behavioral variation is largely unknown. The elevated plus maze, consisting of open and closed arms,...
SourceID proquest
crossref
pubmed
SourceType Aggregation Database
Index Database
StartPage 501
SubjectTerms 3',5'-Cyclic-GMP Phosphodiesterases - genetics
Alleles
Animals
Behavior
Behavior, Animal - physiology
chromosome 5
Chromosome Mapping
Crosses, Genetic
Crossing Over, Genetic
DNA - genetics
DNA Primers - chemistry
Female
Genetic Linkage
Genetic Markers
Genotype
Light
Male
Medical research
Mice
Mice, Inbred A - genetics
Mice, Inbred CBA - genetics
Mutation
Phenotype
Polymerase Chain Reaction
Quantitative Trait, Heritable
Tyr gene
Visual Perception - physiology
Title Quantitative trait loci affecting the behavior of A/J and CBA/J intercross mice in the elevated plus maze
URI https://www.ncbi.nlm.nih.gov/pubmed/11420611
https://www.proquest.com/docview/1021732627
https://search.proquest.com/docview/17899462
https://search.proquest.com/docview/70972255
Volume 12
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3dSxwxEB-qIvgitvXjqrV58KkQ3GTztU9FRRGh0kqFoy9LssmCILvneffiX-9Mbu-kD_Ztl2TZMJNkfpPMzA_gpEzGN1EbbmWIXLlQcK-l5ZWXoahC1UpPCc4_b831vboZ6_Fw4PY8hFUu98S8Uce-oTPyU6Kgtog1pP0xeeLEGkW3qwOFxhpsCFkYCumy45XDJdBFz-nSFS5q9CtWt5pFLiJalppTQJGkYgX6X7v0DtjMRudqB7YHtMjOFur9CB9S9wk2__b5LPwzPPye-y5nieGexYjtYcbQOD0wn6M00CoxxHdsmYrP-padnd4w30V2cU5PVCximgfEiJYe3_MHlHOOGDSyyeMcW_xL2oX7q8s_F9d84E7gTanNjCePonIxNKFIOpaUbFV5IipCxEAmylnfOI0rti2UkjaVNqnK-1aWCRu9K_dgveu7dABM6Fa4gMhOeqG0i86FpFQQpjWmaGwcwfel5OrJokRGvSqGnMVMgXM1ibnWIzhayrYeVstz_abbEXxbNeM8p8sL36V-jn0salAZ-X4PS5WI0EMawf5CZ2-jEQpnhxBf_v_zQ9haRJhRMO4RrM-m8_QVIccsHOd5dQwb55e3v-5eAb2m02A
link.rule.ids 315,783,787,12068,21400,27936,27937,31731,31732,33756,33757,43322,43817,74073,74630
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3fS-QwEB5ORfRF_O3q3pmHezoItmnSpE-yysmep4KgsPhSkiYFQdpVd1_8653Jdld80LeWpDTMJJlvkpn5AH5nIbeVVznXwnkujUu4VULzwgqXFK6ohaUE5-ubfHgvL0dq1B24vXZhlfM9MW7Uvq3ojPyEKKg1Yg2hT8fPnFij6Ha1o9BYghWqw0UMBnq0cLhSdNFjunSBixr9isWtZhKLiGaZ4hRQJKhYgfpsl74Am9HoXGzCRocW2WCm3i34EZptWH1o41n4DjzeTm0Ts8Rwz2LE9jBhaJwemY1RGmiVGOI7Nk_FZ23NBieXzDaenZ_RExWLeIkDYkRLj-_xA8o5Rwzq2fhpii32LezC_cXfu_Mh77gTeJWpfMKDRVEZ7yqXBOUzSrYqLBEVIWIgE2W0rYzCFVsnUgodMh1kYW0tsoCN1mR7sNy0TTgAlqo6NQ6RnbCpVMYb44KULs3rPE8q7XvwZy65cjwrkVEuiiFHMVPgXEliLlUP-nPZlt1qeS0_dNuD40UzznO6vLBNaKfYR6MGZS6-7qGpEhF6SD3Yn-nsYzSpFIhb0sPvf34Ma8O766vy6t_N_yNYn0WbUWBuH5YnL9PwE-HHxP2Kc-wdGpjUrQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1LT9wwEB61i1pxQX1Q2JYWH3qqZJH4nRMCyorSdkWrIqFeIjt2JCSUbGH30l_fGW92EQd6S2RHsWZsz2fPNzMAH2UyvonacCtC5MqFgnstLK-8CEUVqlZ4CnD-PjVnl-r8Sl8N_Ke7gVa52hPzRh37hu7ID6gEtUWsgUf1dqBFXHyeHM7-cKogRZ7WoZzGU9iwyshiBBvHp9OLn2ufAh7Yc_B0hUscTxlrH2eRU4pKqTnRiwSlLtAPrdQj0DOboMkL2BqwIztaKvslPEndK3j2u88346_h-sfCdzlmDHcwRrUf5gxN1TXzmbOBNooh2mOrwHzWt-zo4Jz5LrKTY3qi1BG3eUCMitTje_6AItARkUY2u1lgi_-btuFycvrr5IwPlRR4I7WZ8-RRcC6GJhRJR0mhV5WnskWIH8hgOesbp3H9toVSwiZpk6q8b4VM2OidfAOjru_SLrBSt6ULiPOEL5V20bmQlAqlaY0pGhvH8GkluXq2TJhRr1MjZzETja4mMdd6DHsr2dbD2rmr7zU9hv11M856cmX4LvUL7GNRg8qIx3tYykuE56Ux7Cx1dj-aUglEMeXb__98H57jBKu_fZl-fQebS-oZsXT3YDS_XaT3iEXm4cMwyf4B4x_aSg
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=Quantitative+trait+loci+affecting+the+behavior+of+A%2FJ+and+CBA%2FJ+intercross+mice+in+the+elevated+plus+maze&rft.jtitle=Mammalian+genome&rft.au=Cohen%2C+R+M&rft.au=Kang%2C+A&rft.au=Gulick%2C+C&rft.date=2001-07-01&rft.issn=0938-8990&rft.volume=12&rft.issue=7&rft.spage=501&rft_id=info:doi/10.1007%2Fs00335-001-2047-5&rft_id=info%3Apmid%2F11420611&rft.externalDocID=11420611
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0938-8990&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0938-8990&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0938-8990&client=summon