Effects of GADL1 overexpression on cell migration and the associated morphological changes
Lithium has been used for maintenance treatment of bipolar disorder, but drug response varies among patients. Single-nucleotide polymorphisms in glutamate decarboxylase–like protein 1 ( GADL1 ) are found to be associated with lithium response in Han Chinese bipolar patients. In this study, we assess...
Saved in:
Published in | Scientific reports Vol. 9; no. 1; p. 5298 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
28.03.2019
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Lithium has been used for maintenance treatment of bipolar disorder, but drug response varies among patients. Single-nucleotide polymorphisms in glutamate decarboxylase–like protein 1 (
GADL1
) are found to be associated with lithium response in Han Chinese bipolar patients. In this study, we assessed GADL1 function using a neuroblastoma cell line that stably overexpressed GADL1. Genes encoding factors involved in cell migration, such as
FN1
,
ITGA2
,
ITGAV
and
CCL2
, were downregulated in
GADL1
-overexpressing cells.
GADL1
overexpression indeed suppressed cell migration. Cell migration speed and perimeter length exhibited similar trends, both of which were decreased under
GADL1
overexpression or lithium treatment but increased upon stimulation with CCL2. Secreted GADL1 or its enzyme product, taurine, in the conditioned medium might exert only mild effects on the observed changes. Compared with SH-SY5Y cells,
GADL1
-overexpressing cells were much more sensitive to CCL2 treatment but less sensitive to lithium, indicating that the level of
GADL1
expression can affect cell sensitivity to lithium or CCL2 treatment. Together, these results suggest that cell migration and related morphological changes might provide good indicators of the sensitivity toward lithium treatment, and the
GADL1
stable overexpression cell line might serve as a useful platform to screen novel therapeutics for bipolar disorder. |
---|---|
AbstractList | Lithium has been used for maintenance treatment of bipolar disorder, but drug response varies among patients. Single-nucleotide polymorphisms in glutamate decarboxylase-like protein 1 (GADL1) are found to be associated with lithium response in Han Chinese bipolar patients. In this study, we assessed GADL1 function using a neuroblastoma cell line that stably overexpressed GADL1. Genes encoding factors involved in cell migration, such as FN1, ITGA2, ITGAV and CCL2, were downregulated in GADL1-overexpressing cells. GADL1 overexpression indeed suppressed cell migration. Cell migration speed and perimeter length exhibited similar trends, both of which were decreased under GADL1 overexpression or lithium treatment but increased upon stimulation with CCL2. Secreted GADL1 or its enzyme product, taurine, in the conditioned medium might exert only mild effects on the observed changes. Compared with SH-SY5Y cells, GADL1-overexpressing cells were much more sensitive to CCL2 treatment but less sensitive to lithium, indicating that the level of GADL1 expression can affect cell sensitivity to lithium or CCL2 treatment. Together, these results suggest that cell migration and related morphological changes might provide good indicators of the sensitivity toward lithium treatment, and the GADL1 stable overexpression cell line might serve as a useful platform to screen novel therapeutics for bipolar disorder. Lithium has been used for maintenance treatment of bipolar disorder, but drug response varies among patients. Single-nucleotide polymorphisms in glutamate decarboxylase–like protein 1 ( GADL1 ) are found to be associated with lithium response in Han Chinese bipolar patients. In this study, we assessed GADL1 function using a neuroblastoma cell line that stably overexpressed GADL1. Genes encoding factors involved in cell migration, such as FN1 , ITGA2 , ITGAV and CCL2 , were downregulated in GADL1 -overexpressing cells. GADL1 overexpression indeed suppressed cell migration. Cell migration speed and perimeter length exhibited similar trends, both of which were decreased under GADL1 overexpression or lithium treatment but increased upon stimulation with CCL2. Secreted GADL1 or its enzyme product, taurine, in the conditioned medium might exert only mild effects on the observed changes. Compared with SH-SY5Y cells, GADL1 -overexpressing cells were much more sensitive to CCL2 treatment but less sensitive to lithium, indicating that the level of GADL1 expression can affect cell sensitivity to lithium or CCL2 treatment. Together, these results suggest that cell migration and related morphological changes might provide good indicators of the sensitivity toward lithium treatment, and the GADL1 stable overexpression cell line might serve as a useful platform to screen novel therapeutics for bipolar disorder. Lithium has been used for maintenance treatment of bipolar disorder, but drug response varies among patients. Single-nucleotide polymorphisms in glutamate decarboxylase–like protein 1 (GADL1) are found to be associated with lithium response in Han Chinese bipolar patients. In this study, we assessed GADL1 function using a neuroblastoma cell line that stably overexpressed GADL1. Genes encoding factors involved in cell migration, such as FN1, ITGA2, ITGAV and CCL2, were downregulated in GADL1-overexpressing cells. GADL1 overexpression indeed suppressed cell migration. Cell migration speed and perimeter length exhibited similar trends, both of which were decreased under GADL1 overexpression or lithium treatment but increased upon stimulation with CCL2. Secreted GADL1 or its enzyme product, taurine, in the conditioned medium might exert only mild effects on the observed changes. Compared with SH-SY5Y cells, GADL1-overexpressing cells were much more sensitive to CCL2 treatment but less sensitive to lithium, indicating that the level of GADL1 expression can affect cell sensitivity to lithium or CCL2 treatment. Together, these results suggest that cell migration and related morphological changes might provide good indicators of the sensitivity toward lithium treatment, and the GADL1 stable overexpression cell line might serve as a useful platform to screen novel therapeutics for bipolar disorder. Lithium has been used for maintenance treatment of bipolar disorder, but drug response varies among patients. Single-nucleotide polymorphisms in glutamate decarboxylase-like protein 1 (GADL1) are found to be associated with lithium response in Han Chinese bipolar patients. In this study, we assessed GADL1 function using a neuroblastoma cell line that stably overexpressed GADL1. Genes encoding factors involved in cell migration, such as FN1, ITGA2, ITGAV and CCL2, were downregulated in GADL1-overexpressing cells. GADL1 overexpression indeed suppressed cell migration. Cell migration speed and perimeter length exhibited similar trends, both of which were decreased under GADL1 overexpression or lithium treatment but increased upon stimulation with CCL2. Secreted GADL1 or its enzyme product, taurine, in the conditioned medium might exert only mild effects on the observed changes. Compared with SH-SY5Y cells, GADL1-overexpressing cells were much more sensitive to CCL2 treatment but less sensitive to lithium, indicating that the level of GADL1 expression can affect cell sensitivity to lithium or CCL2 treatment. Together, these results suggest that cell migration and related morphological changes might provide good indicators of the sensitivity toward lithium treatment, and the GADL1 stable overexpression cell line might serve as a useful platform to screen novel therapeutics for bipolar disorder.Lithium has been used for maintenance treatment of bipolar disorder, but drug response varies among patients. Single-nucleotide polymorphisms in glutamate decarboxylase-like protein 1 (GADL1) are found to be associated with lithium response in Han Chinese bipolar patients. In this study, we assessed GADL1 function using a neuroblastoma cell line that stably overexpressed GADL1. Genes encoding factors involved in cell migration, such as FN1, ITGA2, ITGAV and CCL2, were downregulated in GADL1-overexpressing cells. GADL1 overexpression indeed suppressed cell migration. Cell migration speed and perimeter length exhibited similar trends, both of which were decreased under GADL1 overexpression or lithium treatment but increased upon stimulation with CCL2. Secreted GADL1 or its enzyme product, taurine, in the conditioned medium might exert only mild effects on the observed changes. Compared with SH-SY5Y cells, GADL1-overexpressing cells were much more sensitive to CCL2 treatment but less sensitive to lithium, indicating that the level of GADL1 expression can affect cell sensitivity to lithium or CCL2 treatment. Together, these results suggest that cell migration and related morphological changes might provide good indicators of the sensitivity toward lithium treatment, and the GADL1 stable overexpression cell line might serve as a useful platform to screen novel therapeutics for bipolar disorder. |
ArticleNumber | 5298 |
Author | Liu, I-Chao Wu, Tai-Na Wu, Lawrence Shih-Hsin Chen, Chih-Ken Cheng, Andrew Tai-Ann |
Author_xml | – sequence: 1 givenname: Tai-Na surname: Wu fullname: Wu, Tai-Na organization: Institute of Biomedical Sciences, Academia Sinica – sequence: 2 givenname: Chih-Ken surname: Chen fullname: Chen, Chih-Ken organization: School of Medicine, Chang-Gung University and Chang-Gung Memorial Hospital – sequence: 3 givenname: I-Chao surname: Liu fullname: Liu, I-Chao organization: School of Medicine, Fu Jen Catholic University and Fu Jen Catholic University Hospital – sequence: 4 givenname: Lawrence Shih-Hsin surname: Wu fullname: Wu, Lawrence Shih-Hsin email: lshwu@hotmail.com organization: Graduate Institute of Biomedical Sciences, China Medical University – sequence: 5 givenname: Andrew Tai-Ann surname: Cheng fullname: Cheng, Andrew Tai-Ann email: bmandrew@gate.sinica.edu.tw organization: Institute of Biomedical Sciences, Academia Sinica, Graduate Institute of Biomedical Sciences, China Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30923325$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kUtPGzEUha0qVQmUP9AFstRNN0P9mhl7Uwml4SFFYgObbqw7Hk9iNGMHe4LSf1-HAAUWWJZs2d-5vsfnEE188Bahb5ScUsLlzyRoqWRBqCoEraQqtp_QlBFRFowzNnm1P0DHKd2RPEqmBFVf0AEninHOyin6M-86a8aEQ4cvzn4vKA4PNtrtOtqUXPA4T2P7Hg9uGWHcnYBv8biyGFIKxsFoWzyEuF6FPiydgR6bFfilTV_R5w76ZI-f1iN0ez6_mV0Wi-uLq9nZojCiFmMhZM2yC6MIFQ0hTcs5lApo21poOkN4zUkLNTAjmkp1oIgRVSsryDyXFeFH6Ne-7nrTDLY11o8Rer2OboD4Vwdw-u2Ndyu9DA-6ynpV17nAj6cCMdxvbBr14NLONHgbNkkzRkhdKUZ5Rr-_Q-_CJvpsTzOqFJVSyR118rqjl1aevz0DbA-YGFKKtntBKNG7ePU-Xp0_Rj_Gq7dZJN-JjBsfI8muXP-xlO-lKb-Ts4n_2_5A9Q_VzLpe |
CitedBy_id | crossref_primary_10_3390_ijms22168789 crossref_primary_10_1038_s41598_019_46655_1 crossref_primary_10_1016_j_ejphar_2022_174753 |
Cites_doi | 10.1016/j.jpsychires.2011.10.011 10.1023/B:NERE.0000010448.17740.6e 10.1042/BJ20070796 10.1038/tp.2014.72 10.1056/NEJMcp1000402 10.1073/pnas.1700111114 10.1016/j.biopsych.2006.03.065 10.1074/jbc.M112.393728 10.1002/neu.10012 10.1016/S0092-8674(02)00971-6 10.1016/j.neuint.2015.08.013 10.1215/15228517-2008-041 10.1038/ncb2455 10.1016/j.biopsych.2013.01.020 10.1007/s00406-012-0323-x 10.1176/appi.ajp.2014.14070855 10.1152/physrev.1968.48.2.424 10.1111/jnc.12827 10.1007/s11064-013-0977-4 10.1016/j.eurpsy.2011.06.003 10.1523/JNEUROSCI.0156-06.2006 10.1097/YPG.0000000000000066 10.1186/1423-0127-17-S1-S2 10.1002/jnr.22328 10.1176/appi.ajp.163.3.540 10.3109/15622975.2011.559274 10.1046/j.1471-4159.2002.00939.x 10.1016/j.jad.2007.03.003 10.1016/S0140-6736(09)61828-6 10.1056/NEJMoa1212444 10.3389/fncel.2014.00088 10.1038/nn1048 10.1016/S0074-7742(05)71008-4 10.1096/fj.09-151639 10.1111/j.1365-2818.2008.02095.x 10.1038/nrm2957 10.1016/S0140-6736(02)07450-0 10.1016/j.tibs.2008.06.006 10.1016/0896-6273(93)90281-U 10.15252/embr.201540970 10.1523/JNEUROSCI.22-14-05797.2002 |
ContentType | Journal Article |
Copyright | The Author(s) 2019 This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
Copyright_xml | – notice: The Author(s) 2019 – notice: This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
DBID | C6C AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7X7 7XB 88A 88E 88I 8FE 8FH 8FI 8FJ 8FK ABUWG AEUYN AFKRA AZQEC BBNVY BENPR BHPHI CCPQU DWQXO FYUFA GHDGH GNUQQ HCIFZ K9. LK8 M0S M1P M2P M7P PHGZM PHGZT PIMPY PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI Q9U 7X8 5PM |
DOI | 10.1038/s41598-019-41689-x |
DatabaseName | Springer Nature OA Free Journals CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Biology Database (Alumni Edition) Medical Database (Alumni Edition) Science Database (Alumni Edition) ProQuest SciTech Collection ProQuest Natural Science Journals Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest One Sustainability ProQuest Central UK/Ireland ProQuest Central Essentials Biological Science Collection ProQuest Central Natural Science Collection ProQuest One ProQuest Central Korea Proquest Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) ProQuest Biological Science Collection ProQuest Health & Medical Collection Medical Database Science Database (ProQuest) Biological Science Database ProQuest Central Premium ProQuest One Academic (New) ProQuest Publicly Available Content Database ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central Basic MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Publicly Available Content Database ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest One Health & Nursing ProQuest Natural Science Collection ProQuest Biology Journals (Alumni Edition) ProQuest Central ProQuest One Applied & Life Sciences ProQuest One Sustainability ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Health & Medical Research Collection Biological Science Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Science Journals (Alumni Edition) ProQuest Biological Science Collection ProQuest Central Basic ProQuest Science Journals ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE Publicly Available Content Database CrossRef MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: C6C name: Springer Nature OA Free Journals url: http://www.springeropen.com/ sourceTypes: Publisher – sequence: 2 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: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 4 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 2045-2322 |
ExternalDocumentID | PMC6438977 30923325 10_1038_s41598_019_41689_x |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GrantInformation_xml | – fundername: Academia Sinica grantid: AS 23-23, 52102310023C, AS-106-TP-B09; AS 23-23, 52102310023C, AS-106-TP-B09 funderid: https://doi.org/10.13039/501100001869 – fundername: Chang Gung Memorial Hospital, Keelung (grant number: BMRP769) – fundername: Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) grantid: MOST 103-2325-B-001-025; 104-2325-B-001-008; 105-2325-B-001-008; MOST 103-2325-B-001-025; 104-2325-B-001-008; 105-2325-B-001-008 funderid: https://doi.org/10.13039/501100004663 – fundername: ; – fundername: ; grantid: AS 23-23, 52102310023C, AS-106-TP-B09; AS 23-23, 52102310023C, AS-106-TP-B09 – fundername: ; grantid: MOST 103-2325-B-001-025; 104-2325-B-001-008; 105-2325-B-001-008; MOST 103-2325-B-001-025; 104-2325-B-001-008; 105-2325-B-001-008 |
GroupedDBID | 0R~ 3V. 4.4 53G 5VS 7X7 88A 88E 88I 8FE 8FH 8FI 8FJ AAFWJ AAJSJ AAKDD ABDBF ABUWG ACGFS ACSMW ACUHS ADBBV ADRAZ AENEX AEUYN AFKRA AJTQC ALIPV ALMA_UNASSIGNED_HOLDINGS AOIJS AZQEC BAWUL BBNVY BCNDV BENPR BHPHI BPHCQ BVXVI C6C CCPQU DIK DWQXO EBD EBLON EBS EJD ESX FYUFA GNUQQ GROUPED_DOAJ GX1 HCIFZ HH5 HMCUK HYE KQ8 LK8 M0L M1P M2P M48 M7P M~E NAO OK1 PIMPY PQQKQ PROAC PSQYO RNT RNTTT RPM SNYQT UKHRP AASML AAYXX AFPKN CITATION PHGZM PHGZT CGR CUY CVF ECM EIF NPM 7XB 8FK AARCD K9. PJZUB PKEHL PPXIY PQEST PQGLB PQUKI Q9U 7X8 5PM |
ID | FETCH-LOGICAL-c474t-4872019c9014b00bd33a59a1ddeabfc03730da7a2c4b69fa90c46d86a01438603 |
IEDL.DBID | 7X7 |
ISSN | 2045-2322 |
IngestDate | Thu Aug 21 18:31:03 EDT 2025 Thu Jul 10 22:39:12 EDT 2025 Wed Aug 13 08:05:28 EDT 2025 Thu Apr 03 07:06:25 EDT 2025 Tue Jul 01 03:08:33 EDT 2025 Thu Apr 24 22:59:50 EDT 2025 Fri Feb 21 02:38:53 EST 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Language | English |
License | Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c474t-4872019c9014b00bd33a59a1ddeabfc03730da7a2c4b69fa90c46d86a01438603 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
OpenAccessLink | https://www.proquest.com/docview/2199188983?pq-origsite=%requestingapplication% |
PMID | 30923325 |
PQID | 2199188983 |
PQPubID | 2041939 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_6438977 proquest_miscellaneous_2200769213 proquest_journals_2199188983 pubmed_primary_30923325 crossref_primary_10_1038_s41598_019_41689_x crossref_citationtrail_10_1038_s41598_019_41689_x springer_journals_10_1038_s41598_019_41689_x |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2019-03-28 |
PublicationDateYYYYMMDD | 2019-03-28 |
PublicationDate_xml | – month: 03 year: 2019 text: 2019-03-28 day: 28 |
PublicationDecade | 2010 |
PublicationPlace | London |
PublicationPlace_xml | – name: London – name: England |
PublicationTitle | Scientific reports |
PublicationTitleAbbrev | Sci Rep |
PublicationTitleAlternate | Sci Rep |
PublicationYear | 2019 |
Publisher | Nature Publishing Group UK Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group |
References | Mendez, Kojima, Goldman (CR27) 2010; 24 Fan (CR37) 2013; 74 Frye (CR2) 2011; 364 Furukawa (CR32) 2014; 8 Hynes (CR23) 2002; 110 CR36 Oja, Saransaari (CR14) 2007; 50 Hernandez-Benitez, Pasantes-Morales, Saldana, Ramos-Mandujano (CR15) 2010; 88 Belmadani, Tran, Ren, Miller (CR24) 2006; 26 Tobe (CR31) 2017; 114 Boer (CR42) 2007; 408 Fountoulakis (CR4) 2012; 262 Chen (CR8) 2014; 370 Pardo (CR29) 2016; 17 Jacobsen, Smith (CR12) 1968; 48 Eastwood, Harrison (CR34) 2006; 163 Liu (CR11) 2012; 287 Geddes (CR3) 2010; 375 Nacher, Guirado, Castillo-Gomez (CR38) 2013; 38 Rybakowski (CR7) 2011; 12 Parsons, Horwitz, Schwartz (CR22) 2010; 11 Carleton, Petreanu, Lansford, Alvarez-Buylla, Lledo (CR21) 2003; 6 Wang (CR26) 2014; 4 Muller-Oerlinghausen, Berghofer, Bauer (CR1) 2002; 359 Cruceanu, Alda, Dion, Turecki, Rouleau (CR9) 2015; 172 Luskin (CR19) 1993; 11 El Idrissi, Trenkner (CR17) 2004; 29 De Marchis, Fasolo, Shipley, Puche (CR20) 2001; 49 Poon, Ho, Barson, Leibowitz (CR25) 2014; 131 Schaffer, Jong, Ramila, Azuma (CR13) 2010; 17 Garnham (CR6) 2007; 104 Kotambail (CR10) 2015; 25 Wasserman (CR5) 2012; 27 Yang (CR28) 2012; 14 Molder (CR40) 2008; 232 Mai, Jope, Li (CR41) 2002; 82 Nowicki (CR30) 2008; 10 Ishizuka, Paek, Kamiya, Sawa (CR33) 2006; 59 Varea (CR39) 2012; 46 Fatemi (CR35) 2005; 71 Winge (CR18) 2015; 90 Banerjee, Vitvitsky, Garg (CR16) 2008; 33 MA Frye (41689_CR2) 2011; 364 R Banerjee (41689_CR16) 2008; 33 P Liu (41689_CR11) 2012; 287 RO Hynes (41689_CR23) 2002; 110 K Ishizuka (41689_CR33) 2006; 59 Y Fan (41689_CR37) 2013; 74 JL Wang (41689_CR26) 2014; 4 L Mai (41689_CR41) 2002; 82 JG Jacobsen (41689_CR12) 1968; 48 JR Geddes (41689_CR3) 2010; 375 OE Pardo (41689_CR29) 2016; 17 C Cruceanu (41689_CR9) 2015; 172 D Wasserman (41689_CR5) 2012; 27 SS Oja (41689_CR14) 2007; 50 A Belmadani (41689_CR24) 2006; 26 I Winge (41689_CR18) 2015; 90 WH Yang (41689_CR28) 2012; 14 SW Schaffer (41689_CR13) 2010; 17 KN Fountoulakis (41689_CR4) 2012; 262 MO Nowicki (41689_CR30) 2008; 10 A Molder (41689_CR40) 2008; 232 R Hernandez-Benitez (41689_CR15) 2010; 88 U Boer (41689_CR42) 2007; 408 41689_CR36 MB Luskin (41689_CR19) 1993; 11 CH Chen (41689_CR8) 2014; 370 A El Idrissi (41689_CR17) 2004; 29 SH Fatemi (41689_CR35) 2005; 71 A Carleton (41689_CR21) 2003; 6 A Kotambail (41689_CR10) 2015; 25 J Garnham (41689_CR6) 2007; 104 JK Rybakowski (41689_CR7) 2011; 12 S De Marchis (41689_CR20) 2001; 49 J Nacher (41689_CR38) 2013; 38 JT Parsons (41689_CR22) 2010; 11 BTD Tobe (41689_CR31) 2017; 114 T Furukawa (41689_CR32) 2014; 8 SL Eastwood (41689_CR34) 2006; 163 E Varea (41689_CR39) 2012; 46 B Muller-Oerlinghausen (41689_CR1) 2002; 359 K Poon (41689_CR25) 2014; 131 MG Mendez (41689_CR27) 2010; 24 |
References_xml | – volume: 46 start-page: 189 year: 2012 end-page: 197 ident: CR39 article-title: Expression of PSA-NCAM and synaptic proteins in the amygdala of psychiatric disorder patients publication-title: J Psychiatr Res doi: 10.1016/j.jpsychires.2011.10.011 – volume: 29 start-page: 189 year: 2004 end-page: 197 ident: CR17 article-title: Taurine as a modulator of excitatory and inhibitory neurotransmission publication-title: Neurochem. Res. doi: 10.1023/B:NERE.0000010448.17740.6e – volume: 408 start-page: 69 year: 2007 end-page: 77 ident: CR42 article-title: Enhancement by lithium of cAMP-induced CRE/CREB-directed gene transcription conferred by TORC on the CREB basic leucine zipper domain publication-title: Biochem. J. doi: 10.1042/BJ20070796 – volume: 4 year: 2014 ident: CR26 article-title: Label-free, live optical imaging of reprogrammed bipolar disorder patient-derived cells reveals a functional correlate of lithium responsiveness publication-title: Transl Psychiatry doi: 10.1038/tp.2014.72 – volume: 364 start-page: 51 year: 2011 end-page: 59 ident: CR2 article-title: Clinical practice. Bipolar disorder–a focus on depression publication-title: N Engl J Med doi: 10.1056/NEJMcp1000402 – volume: 114 start-page: E4462 year: 2017 end-page: E4471 ident: CR31 article-title: Probing the lithium-response pathway in hiPSCs implicates the phosphoregulatory set-point for a cytoskeletal modulator in bipolar pathogenesis publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.1700111114 – volume: 59 start-page: 1189 year: 2006 end-page: 1197 ident: CR33 article-title: A review of Disrupted-In-Schizophrenia-1 (DISC1): neurodevelopment, cognition, and mental conditions publication-title: Biol. Psychiatry doi: 10.1016/j.biopsych.2006.03.065 – volume: 287 start-page: 40898 year: 2012 end-page: 40906 ident: CR11 article-title: Role of glutamate decarboxylase-like protein 1 (GADL1) in taurine biosynthesis publication-title: J. Biol. Chem. doi: 10.1074/jbc.M112.393728 – volume: 49 start-page: 326 year: 2001 end-page: 338 ident: CR20 article-title: Unique neuronal tracers show migration and differentiation of SVZ progenitors in organotypic slices publication-title: J. Neurobiol. doi: 10.1002/neu.10012 – volume: 110 start-page: 673 year: 2002 end-page: 687 ident: CR23 article-title: Integrins: bidirectional, allosteric signaling machines publication-title: Cell doi: 10.1016/S0092-8674(02)00971-6 – volume: 90 start-page: 173 year: 2015 end-page: 184 ident: CR18 article-title: Mammalian CSAD and GADL1 have distinct biochemical properties and patterns of brain expression publication-title: Neurochem. Int. doi: 10.1016/j.neuint.2015.08.013 – volume: 10 start-page: 690 year: 2008 end-page: 699 ident: CR30 article-title: Lithium inhibits invasion of glioma cells; possible involvement of glycogen synthase kinase-3 publication-title: Neuro Oncol doi: 10.1215/15228517-2008-041 – volume: 14 start-page: 366 year: 2012 end-page: 374 ident: CR28 article-title: RAC1 activation mediates Twist1-induced cancer cell migration publication-title: Nat. Cell Biol. doi: 10.1038/ncb2455 – volume: 74 start-page: 418 year: 2013 end-page: 426 ident: CR37 article-title: Focal adhesion dynamics are altered in schizophrenia publication-title: Biol. Psychiatry doi: 10.1016/j.biopsych.2013.01.020 – volume: 262 start-page: 1 issue: Suppl 1 year: 2012 end-page: 48 ident: CR4 article-title: Efficacy of pharmacotherapy in bipolar disorder: a report by the WPA section on pharmacopsychiatry publication-title: European archives of psychiatry and clinical neuroscience doi: 10.1007/s00406-012-0323-x – volume: 172 start-page: 94 year: 2015 end-page: 95 ident: CR9 article-title: No evidence for GADL1 variation as a bipolar disorder susceptibility factor in a Caucasian lithium-responsive cohort publication-title: Am. J. Psychiatry doi: 10.1176/appi.ajp.2014.14070855 – volume: 48 start-page: 424 year: 1968 end-page: 511 ident: CR12 article-title: Biochemistry and physiology of taurine and taurine derivatives publication-title: Physiol. Rev. doi: 10.1152/physrev.1968.48.2.424 – volume: 50 start-page: 8 year: 2007 end-page: 15 ident: CR14 article-title: Pharmacology of taurine publication-title: Proc. West. Pharmacol. Soc. – volume: 131 start-page: 509 year: 2014 end-page: 520 ident: CR25 article-title: Stimulatory role of the chemokine CCL2 in the migration and peptide expression of embryonic hypothalamic neurons publication-title: J. Neurochem. doi: 10.1111/jnc.12827 – volume: 38 start-page: 1122 year: 2013 end-page: 1133 ident: CR38 article-title: Structural plasticity of interneurons in the adult brain: role of PSA-NCAM and implications for psychiatric disorders publication-title: Neurochem. Res. doi: 10.1007/s11064-013-0977-4 – volume: 27 start-page: 129 year: 2012 end-page: 141 ident: CR5 article-title: The European Psychiatric Association (EPA) guidance on suicide treatment and prevention publication-title: European psychiatry: the journal of the Association of European Psychiatrists doi: 10.1016/j.eurpsy.2011.06.003 – volume: 26 start-page: 3182 year: 2006 end-page: 3191 ident: CR24 article-title: Chemokines regulate the migration of neural progenitors to sites of neuroinflammation publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.0156-06.2006 – volume: 25 start-page: 39 year: 2015 end-page: 40 ident: CR10 article-title: GADL1 gene polymorphisms and lithium response in bipolar I disorder: lack of association from an Indian population publication-title: Psychiatr. Genet. doi: 10.1097/YPG.0000000000000066 – volume: 17 start-page: S2 issue: Suppl 1 year: 2010 ident: CR13 article-title: Physiological roles of taurine in heart and muscle publication-title: J. Biomed. Sci. doi: 10.1186/1423-0127-17-S1-S2 – volume: 88 start-page: 1673 year: 2010 end-page: 1681 ident: CR15 article-title: Taurine stimulates proliferation of mice embryonic cultured neural progenitor cells publication-title: J. Neurosci. Res. doi: 10.1002/jnr.22328 – volume: 163 start-page: 540 year: 2006 end-page: 542 ident: CR34 article-title: Cellular basis of reduced cortical reelin expression in schizophrenia publication-title: Am. J. Psychiatry doi: 10.1176/appi.ajp.163.3.540 – volume: 12 start-page: 340 year: 2011 end-page: 348 ident: CR7 article-title: Lithium in neuropsychiatry: a 2010 update publication-title: World J. Biol. Psychiatry doi: 10.3109/15622975.2011.559274 – volume: 82 start-page: 75 year: 2002 end-page: 83 ident: CR41 article-title: BDNF-mediated signal transduction is modulated by GSK3beta and mood stabilizing agents publication-title: J. Neurochem. doi: 10.1046/j.1471-4159.2002.00939.x – volume: 104 start-page: 185 year: 2007 end-page: 190 ident: CR6 article-title: Prophylactic treatment response in bipolar disorder: results of a naturalistic observation study publication-title: J. Affect. Disord. doi: 10.1016/j.jad.2007.03.003 – volume: 375 start-page: 385 year: 2010 end-page: 395 ident: CR3 article-title: Lithium plus valproate combination therapy versus monotherapy for relapse prevention in bipolar I disorder (BALANCE): a randomised open-label trial publication-title: Lancet doi: 10.1016/S0140-6736(09)61828-6 – volume: 370 start-page: 119 year: 2014 end-page: 128 ident: CR8 article-title: Variant GADL1 and response to lithium therapy in bipolar I disorder publication-title: N. Engl. J. Med. doi: 10.1056/NEJMoa1212444 – volume: 8 start-page: 88 year: 2014 ident: CR32 article-title: Roles of taurine-mediated tonic GABAA receptor activation in the radial migration of neurons in the fetal mouse cerebral cortex publication-title: Front Cell Neurosci doi: 10.3389/fncel.2014.00088 – volume: 6 start-page: 507 year: 2003 end-page: 518 ident: CR21 article-title: Becoming a new neuron in the adult olfactory bulb publication-title: Nat. Neurosci. doi: 10.1038/nn1048 – volume: 71 start-page: 179 year: 2005 end-page: 187 ident: CR35 article-title: Reelin glycoprotein in autism and schizophrenia publication-title: Int. Rev. Neurobiol. doi: 10.1016/S0074-7742(05)71008-4 – ident: CR36 – volume: 24 start-page: 1838 year: 2010 end-page: 1851 ident: CR27 article-title: Vimentin induces changes in cell shape, motility, and adhesion during the epithelial to mesenchymal transition publication-title: FASEB J. doi: 10.1096/fj.09-151639 – volume: 232 start-page: 240 year: 2008 end-page: 247 ident: CR40 article-title: Non-invasive, label-free cell counting and quantitative analysis of adherent cells using digital holography publication-title: J. Microsc. doi: 10.1111/j.1365-2818.2008.02095.x – volume: 11 start-page: 633 year: 2010 end-page: 643 ident: CR22 article-title: Cell adhesion: integrating cytoskeletal dynamics and cellular tension publication-title: Nat. Rev. Mol. Cell Biol. doi: 10.1038/nrm2957 – volume: 359 start-page: 241 year: 2002 end-page: 247 ident: CR1 article-title: Bipolar disorder publication-title: Lancet doi: 10.1016/S0140-6736(02)07450-0 – volume: 33 start-page: 413 year: 2008 end-page: 419 ident: CR16 article-title: The undertow of sulfur metabolism on glutamatergic neurotransmission publication-title: Trends Biochem. Sci. doi: 10.1016/j.tibs.2008.06.006 – volume: 11 start-page: 173 year: 1993 end-page: 189 ident: CR19 article-title: Restricted proliferation and migration of postnatally generated neurons derived from the forebrain subventricular zone publication-title: Neuron doi: 10.1016/0896-6273(93)90281-U – volume: 17 start-page: 570 year: 2016 end-page: 584 ident: CR29 article-title: miR-515-5p controls cancer cell migration through MARK4 regulation publication-title: EMBO Rep doi: 10.15252/embr.201540970 – volume: 4 year: 2014 ident: 41689_CR26 publication-title: Transl Psychiatry doi: 10.1038/tp.2014.72 – volume: 8 start-page: 88 year: 2014 ident: 41689_CR32 publication-title: Front Cell Neurosci doi: 10.3389/fncel.2014.00088 – ident: 41689_CR36 doi: 10.1523/JNEUROSCI.22-14-05797.2002 – volume: 74 start-page: 418 year: 2013 ident: 41689_CR37 publication-title: Biol. Psychiatry doi: 10.1016/j.biopsych.2013.01.020 – volume: 359 start-page: 241 year: 2002 ident: 41689_CR1 publication-title: Lancet doi: 10.1016/S0140-6736(02)07450-0 – volume: 12 start-page: 340 year: 2011 ident: 41689_CR7 publication-title: World J. Biol. Psychiatry doi: 10.3109/15622975.2011.559274 – volume: 50 start-page: 8 year: 2007 ident: 41689_CR14 publication-title: Proc. West. Pharmacol. Soc. – volume: 24 start-page: 1838 year: 2010 ident: 41689_CR27 publication-title: FASEB J. doi: 10.1096/fj.09-151639 – volume: 90 start-page: 173 year: 2015 ident: 41689_CR18 publication-title: Neurochem. Int. doi: 10.1016/j.neuint.2015.08.013 – volume: 11 start-page: 173 year: 1993 ident: 41689_CR19 publication-title: Neuron doi: 10.1016/0896-6273(93)90281-U – volume: 26 start-page: 3182 year: 2006 ident: 41689_CR24 publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.0156-06.2006 – volume: 408 start-page: 69 year: 2007 ident: 41689_CR42 publication-title: Biochem. J. doi: 10.1042/BJ20070796 – volume: 82 start-page: 75 year: 2002 ident: 41689_CR41 publication-title: J. Neurochem. doi: 10.1046/j.1471-4159.2002.00939.x – volume: 33 start-page: 413 year: 2008 ident: 41689_CR16 publication-title: Trends Biochem. Sci. doi: 10.1016/j.tibs.2008.06.006 – volume: 163 start-page: 540 year: 2006 ident: 41689_CR34 publication-title: Am. J. Psychiatry doi: 10.1176/appi.ajp.163.3.540 – volume: 27 start-page: 129 year: 2012 ident: 41689_CR5 publication-title: European psychiatry: the journal of the Association of European Psychiatrists doi: 10.1016/j.eurpsy.2011.06.003 – volume: 262 start-page: 1 issue: Suppl 1 year: 2012 ident: 41689_CR4 publication-title: European archives of psychiatry and clinical neuroscience doi: 10.1007/s00406-012-0323-x – volume: 17 start-page: 570 year: 2016 ident: 41689_CR29 publication-title: EMBO Rep doi: 10.15252/embr.201540970 – volume: 46 start-page: 189 year: 2012 ident: 41689_CR39 publication-title: J Psychiatr Res doi: 10.1016/j.jpsychires.2011.10.011 – volume: 104 start-page: 185 year: 2007 ident: 41689_CR6 publication-title: J. Affect. Disord. doi: 10.1016/j.jad.2007.03.003 – volume: 370 start-page: 119 year: 2014 ident: 41689_CR8 publication-title: N. Engl. J. Med. doi: 10.1056/NEJMoa1212444 – volume: 25 start-page: 39 year: 2015 ident: 41689_CR10 publication-title: Psychiatr. Genet. doi: 10.1097/YPG.0000000000000066 – volume: 6 start-page: 507 year: 2003 ident: 41689_CR21 publication-title: Nat. Neurosci. doi: 10.1038/nn1048 – volume: 287 start-page: 40898 year: 2012 ident: 41689_CR11 publication-title: J. Biol. Chem. doi: 10.1074/jbc.M112.393728 – volume: 14 start-page: 366 year: 2012 ident: 41689_CR28 publication-title: Nat. Cell Biol. doi: 10.1038/ncb2455 – volume: 114 start-page: E4462 year: 2017 ident: 41689_CR31 publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.1700111114 – volume: 17 start-page: S2 issue: Suppl 1 year: 2010 ident: 41689_CR13 publication-title: J. Biomed. Sci. doi: 10.1186/1423-0127-17-S1-S2 – volume: 232 start-page: 240 year: 2008 ident: 41689_CR40 publication-title: J. Microsc. doi: 10.1111/j.1365-2818.2008.02095.x – volume: 48 start-page: 424 year: 1968 ident: 41689_CR12 publication-title: Physiol. Rev. doi: 10.1152/physrev.1968.48.2.424 – volume: 38 start-page: 1122 year: 2013 ident: 41689_CR38 publication-title: Neurochem. Res. doi: 10.1007/s11064-013-0977-4 – volume: 88 start-page: 1673 year: 2010 ident: 41689_CR15 publication-title: J. Neurosci. Res. doi: 10.1002/jnr.22328 – volume: 10 start-page: 690 year: 2008 ident: 41689_CR30 publication-title: Neuro Oncol doi: 10.1215/15228517-2008-041 – volume: 71 start-page: 179 year: 2005 ident: 41689_CR35 publication-title: Int. Rev. Neurobiol. doi: 10.1016/S0074-7742(05)71008-4 – volume: 172 start-page: 94 year: 2015 ident: 41689_CR9 publication-title: Am. J. Psychiatry doi: 10.1176/appi.ajp.2014.14070855 – volume: 131 start-page: 509 year: 2014 ident: 41689_CR25 publication-title: J. Neurochem. doi: 10.1111/jnc.12827 – volume: 11 start-page: 633 year: 2010 ident: 41689_CR22 publication-title: Nat. Rev. Mol. Cell Biol. doi: 10.1038/nrm2957 – volume: 29 start-page: 189 year: 2004 ident: 41689_CR17 publication-title: Neurochem. Res. doi: 10.1023/B:NERE.0000010448.17740.6e – volume: 59 start-page: 1189 year: 2006 ident: 41689_CR33 publication-title: Biol. Psychiatry doi: 10.1016/j.biopsych.2006.03.065 – volume: 49 start-page: 326 year: 2001 ident: 41689_CR20 publication-title: J. Neurobiol. doi: 10.1002/neu.10012 – volume: 110 start-page: 673 year: 2002 ident: 41689_CR23 publication-title: Cell doi: 10.1016/S0092-8674(02)00971-6 – volume: 375 start-page: 385 year: 2010 ident: 41689_CR3 publication-title: Lancet doi: 10.1016/S0140-6736(09)61828-6 – volume: 364 start-page: 51 year: 2011 ident: 41689_CR2 publication-title: N Engl J Med doi: 10.1056/NEJMcp1000402 |
SSID | ssj0000529419 |
Score | 2.3174365 |
Snippet | Lithium has been used for maintenance treatment of bipolar disorder, but drug response varies among patients. Single-nucleotide polymorphisms in glutamate... |
SourceID | pubmedcentral proquest pubmed crossref springer |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 5298 |
SubjectTerms | 14 14/63 38/109 38/61 38/77 38/90 631/337/2019 631/80/84 Antimanic Agents - pharmacology Antimanic Agents - therapeutic use Asian Continental Ancestry Group - genetics Bipolar disorder Bipolar Disorder - drug therapy Bipolar Disorder - genetics Carboxy-Lyases - genetics Carboxy-Lyases - metabolism Cell adhesion & migration Cell Line, Tumor Cell migration Cell Movement - drug effects Cell Movement - genetics Chemokine CCL2 - metabolism Drug Resistance - genetics Glutamate decarboxylase Humanities and Social Sciences Humans Lithium Lithium - pharmacology Lithium - therapeutic use Monocyte chemoattractant protein 1 Morphology multidisciplinary Neurons - physiology Patients Polymorphism, Single Nucleotide Science Science (multidisciplinary) Single-nucleotide polymorphism Taurine |
SummonAdditionalLinks | – databaseName: Scholars Portal Journals: Open Access dbid: M48 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfR1daxQxcCiVgi-itupqLRF809XNx2aTB5FSrUWsTx4UX5Ykm20L7V7tXeH6753Z7F45Wwv7loRN5iMzk_kCeNsGq6T3aJ2oUOZK00OTljwXjVciWjSL-lyYw5_6YKK-H5VHazC2OxoAOLvTtKN-UpPLsw-LP9efkeE_pZRx83GGQogSxTj5NLWxOeqUD1AyVcSoh4O6n2p9C6u4HXJn7l66Kp9uKZ23Yyf_caD2cmn_MTwaFEq2myjgCazF7ilspBaT15vwO5UnnrFpy77tfvnBGcVsxsUQ_9ox_Ojxnp2fHidiYK5rGKqFzA2Yiw07nyI6xmuSpWTh2RZM9r_-2jvIh34KeVCVmudom6C4t4E8p8htvpHSldZxvOGcb0OBaCkaVzkRlNe2dbYISjdGO6oBaHQhn8F6N-3iC2BVK5TRTeFLJ5WLyqFlUhahCNwr7mKbAR-hWIeh2Dj1vDire6e3NHWCfI37qXvI14sM3i3XXKRSG_fO3h6RU49UUwsK5DLGGpnBm-UwMgwB0nVxeoVz6HVWW8FxzvOEy-XvZIH6rhRlBtUKlpcTqBj36kh3etIX5dbURr6qMng_0sPNtv5_ipf3n-IVPCSMUcybMNuwPr-8iq9RCZr7nZ6y_wIJzgLQ priority: 102 providerName: Scholars Portal – databaseName: Springer Nature OA Free Journals dbid: C6C link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1baxUxEB5KRfBF6n1rLRF808XcNps8lqO1FPXJQvFlSbJZLbR7xHMK9d87k73IsVUo7NtO2OxMkpnM5RuAV110WoWAtxMdq1IbcjQZJUrZBi2Tw2tRroX59Nkcnejj0-p0C-RUC5OT9jOkZT6mp-ywtytUNFQMJihuaawr0W68Q9DttKoXZjH7VShypYUb62O4sjcM3dRB1wzL6_mRfwVJs-453IH7o9HIDoZpPoCt1D-Eu0MbyV-P4OsAQbxiy459OHj3UTDKy0xXY45rz_AhBz27OPs2CJz5vmVo-jE_Sie17GKJLJ-OQjYUBK8ew8nh-y-Lo3LsmVBGXet1ifcPVOkuUnQUd1RolfKV8wJPMR-6yJH1vPW1l1EH4zrveNSmtcYTzp81XD2B7X7Zp2fA6k5qa1oeKq-0T9rj7aPikUcRtPCpK0BMXGziCChOfS3OmxzYVrYZON_gfJrM-eaqgNfzmB8DnMZ_qfcm4TTj1lo1kpK1rHVWFfByfo2bghjp-7S8RBrywBonBdI8HWQ5f05xtGmVrAqoN6Q8ExDg9uab_ux7Bt421Cq-rgt4M62HP9P691_s3o78OdwjCVKem7R7sL3-eZleoOGzDvt5pf8G-JT9pA priority: 102 providerName: Springer Nature |
Title | Effects of GADL1 overexpression on cell migration and the associated morphological changes |
URI | https://link.springer.com/article/10.1038/s41598-019-41689-x https://www.ncbi.nlm.nih.gov/pubmed/30923325 https://www.proquest.com/docview/2199188983 https://www.proquest.com/docview/2200769213 https://pubmed.ncbi.nlm.nih.gov/PMC6438977 |
Volume | 9 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfR1da9wwzGwtg72M7jtdd3iwty3UiR3Hfiq3W7tyrGVsKxx7CbbjdIU1aZcrXP99pcRJuZUVQgKxQmzJlmRJlgh5XzktuLWwOxEui4VEQ5PkSZyWVqRew7aoOwtzdCwPT8R8kS2Cwa0NYZUDT-wYddk4tJHvphijo5RWfO_iMsaqUehdDSU0HpJNTF2GIV35Ih9tLOjFEokOZ2UYV7styCs8U5ag-1MqHa_W5dEdJfNurOQ_DtNODh1skSdBgaTTnuJPyQNfPyOP-pKS18_Jrz4dcUubin6Zfv6aUIzR9KsQ71pTuNBYT8_PTnviU1OXFNRAagKlfEnPG0D_wBZpfzi4fUFODvZ_zg7jUD8hdiIXyxj2IiDetUNPKawuW3JuMm0S4GjGVo4BGVhpcpM6YaWujGZOyFJJgzn_lGT8Jdmom9q_JjSvUqFkyWxmuDBeGNiJZMwxl1iRGF9FJBmwWLiQXBxrXPwpOic3V0WP-QL6U3SYL1YR-TB-c9Gn1rgXemcgThGWWVvcToqIvBubYYEgIk3tmyuAQWus1GkCMK96Wo6_4wz0W55mEcnXqDwCYPLt9Zb67HeXhFti2fg8j8jHYT7cduv_o9i-fxRvyGOkGMa4pWqHbCz_Xvm3oPQs7aSb2ROyOZ3Of8zh-Wn_-Nt3eDuTs0lnSID7kVA3yvAFMw |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtR1dT9Uw9AQvMfpi_HaKWhN90oWt7br1wRgU8CKXG2MgIbzMruuARDZ0l3j5U_5Gz9kXuRJ5I9lbu609H-35PgCvC6ulyDLUTqSNfKnI0KRE6PM8k9xpVIuaXJidqRrvyS_70f4S_OlzYSissj8Tm4M6ryzZyFc5xegkiU7Eh9OfPnWNIu9q30KjJYttd_4bVbb6_dY64vcN55sbu5_GftdVwLcyljMfJXS89LQl_yHSXJYLYSJtQuRzkxU2wMUFuYkNtzJTujA6sFLliTJUCS9RgcDv3oBlKVCVGcHyx43p12-DVYf8ZjLUXXZOIJLVGm9IymILyeGqEu3PF2_AS2Lt5ejMf1y0zc23eRfudCIrW2tp7B4sufI-3GybWJ4_gIO2AHLNqoJ9XlufhIyiQt28i7AtGT7kHmAnx4ctuTFT5gwFT2Y62nA5O6kQ4f1BzNp05Poh7F0LbB_BqKxK9wRYXHCZqDzIIiOkcdKg7hMFNrBhJkPjCg_CHoqp7cqZU1eNH2njVhdJ2kI-xfWkDeTTuQdvh3dO22IeV85e6ZGTdoxdpxdk6MGrYRhZkgBpSled4Ryy_yrNQ5zzuMXl8DsRoEQteORBvIDlYQKV-14cKY-PmrLfihrVx7EH73p6uFjW_3fx9OpdvIRb492dSTrZmm4_g9uEPYqw48kKjGa_ztxzFLlm2YuOzhl8v27W-gvOazzG |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtR3LbtQwcFSKQFwQbwIFjAQniDZ-xHEOCFUsS0tLxYFKKy6p4zhQiSaFbMX21_g6ZvKqloreKuXmSWLPwzP2vABelC5VMs_xdKJcHCpNF01a8lAUuRI-xWNRmwvzaU9v7auP83i-Bn-GXBgKqxz2xHajLmpHd-QTQTE6xqRGTso-LOLzdPb2-GdIHaTI0zq00-hYZMef_sbjW_Nme4q0finE7P2Xd1th32EgdCpRixCtdVSAqSNfIvJfXkhp49RylHmbly7CiUaFTaxwKtdpadPIKV0YbakqntGRxO9egauJjDnJWDJPxvsd8qApnvZ5OpE0kwZ1JeWzcXK9apOGy1VdeM7APR-n-Y-zttWBs1twszde2WbHbbdhzVd34FrXzvL0LnztSiE3rC7Zh83pLmcUH-qXfaxtxfAhRwE7OvzWMR6zVcHQBGW25xJfsKMaST9syaxLTG7uwf6lYPY-rFd15R8CS0qhjC6iPLZSWa8snoLiyEWO54pbXwbAByxmri9sTv01fmStg12arMN8hvPJWsxnywBeje8cd2U9LoTeGIiT9SLeZGcMGcDzcRiFkxBpK1-fIAzdBOtUcIR50NFy_J2M0LaWIg4gWaHyCECFv1dHqsPvbQFwTS3rkySA1wM_nE3r_6t4dPEqnsF1FKhsd3tv5zHcIOJRqJ0wG7C--HXin6DttciftkzO4OCypeovHYs_lg |
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=Effects+of+GADL1+overexpression+on+cell+migration+and+the+associated+morphological+changes&rft.jtitle=Scientific+reports&rft.au=Tai-Na%2C+Wu&rft.au=Chen+Chih-Ken&rft.au=I-Chao%2C+Liu&rft.au=Wu+Lawrence+Shih-Hsin&rft.date=2019-03-28&rft.pub=Nature+Publishing+Group&rft.eissn=2045-2322&rft.volume=9&rft.issue=1&rft_id=info:doi/10.1038%2Fs41598-019-41689-x&rft.externalDBID=HAS_PDF_LINK |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2045-2322&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2045-2322&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2045-2322&client=summon |