Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians
Variants in genes involved in pancreatic β-cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with complex form. In this study, we studied the genetic association of polymorphisms in such important genes with type 2 diabetes in the high-risk I...
Saved in:
| Published in | Journal of human genetics Vol. 56; no. 10; pp. 695 - 700 |
|---|---|
| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
Nature Publishing Group UK
01.10.2011
Nature Publishing Group |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1434-5161 1435-232X 1435-232X |
| DOI | 10.1038/jhg.2011.83 |
Cover
| Abstract | Variants in genes involved in pancreatic β-cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with complex form. In this study, we studied the genetic association of polymorphisms in such important genes with type 2 diabetes in the high-risk Indians. We genotyped 91 polymorphisms in 19 genes (
ABCC8, HNF1A, HNF1B, HNF4A, INS, INSM1
,
ISL1, KCNJ11, MAFA, MNX1, NEUROD1, NEUROG3, NKX2.2, NKX6.1, PAX4, PAX6, PDX1, USF1
and
WFS1
) in 2025 unrelated North Indians of Indo-European ethnicity comprising of 1019 diabetic and 1006 non-diabetic subjects.
HNF4A
promoter P2 polymorphisms rs1884613 and rs2144908, which are in high linkage disequilibrium, showed significant association with type 2 diabetes (odds ratio (OR)=1.37 (95% confidence interval (CI) 1.19–1.57),
P
=9.4 × 10
−6
for rs1884613 and OR=1.37 (95%CI 1.20–1.57),
P
=6.0 × 10
−6
for rs2144908), as previously shown in other populations. We observed body mass index-dependent association of these variants with type 2 diabetes in normal-weight/lean subjects. Variants in
USF1
,
ABCC8
,
ISL1
and
KCNJ11
showed nominal association, while haplotypes in these genes were significantly associated. rs3812704 upstream of
NEUROG3
significantly increased risk for type 2 diabetes in normal-weight/lean subjects (OR=1.68 (95%CI 1.25–2.24),
P
=4.9 × 10
−4
). Thus, pancreatic β-cell development and function genes contribute to susceptibility to type 2 diabetes in North Indians. |
|---|---|
| AbstractList | Variants in genes involved in pancreatic β-cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with complex form. In this study, we studied the genetic association of polymorphisms in such important genes with type 2 diabetes in the high-risk Indians. We genotyped 91 polymorphisms in 19 genes (ABCC8, HNF1A, HNF1B, HNF4A, INS, INSM1, ISL1, KCNJ11, MAFA, MNX1, NEUROD1, NEUROG3, NKX2.2, NKX6.1, PAX4, PAX6, PDX1, USF1 and WFS1) in 2025 unrelated North Indians of Indo-European ethnicity comprising of 1019 diabetic and 1006 non-diabetic subjects. HNF4A promoter P2 polymorphisms rs1884613 and rs2144908, which are in high linkage disequilibrium, showed significant association with type 2 diabetes (odds ratio (OR)=1.37 (95% confidence interval (CI) 1.19-1.57), P=9.4 × 10(-6) for rs1884613 and OR=1.37 (95%CI 1.20-1.57), P=6.0 × 10(-6) for rs2144908), as previously shown in other populations. We observed body mass index-dependent association of these variants with type 2 diabetes in normal-weight/lean subjects. Variants in USF1, ABCC8, ISL1 and KCNJ11 showed nominal association, while haplotypes in these genes were significantly associated. rs3812704 upstream of NEUROG3 significantly increased risk for type 2 diabetes in normal-weight/lean subjects (OR=1.68 (95%CI 1.25-2.24), P=4.9 × 10(-4)). Thus, pancreatic β-cell development and function genes contribute to susceptibility to type 2 diabetes in North Indians.Variants in genes involved in pancreatic β-cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with complex form. In this study, we studied the genetic association of polymorphisms in such important genes with type 2 diabetes in the high-risk Indians. We genotyped 91 polymorphisms in 19 genes (ABCC8, HNF1A, HNF1B, HNF4A, INS, INSM1, ISL1, KCNJ11, MAFA, MNX1, NEUROD1, NEUROG3, NKX2.2, NKX6.1, PAX4, PAX6, PDX1, USF1 and WFS1) in 2025 unrelated North Indians of Indo-European ethnicity comprising of 1019 diabetic and 1006 non-diabetic subjects. HNF4A promoter P2 polymorphisms rs1884613 and rs2144908, which are in high linkage disequilibrium, showed significant association with type 2 diabetes (odds ratio (OR)=1.37 (95% confidence interval (CI) 1.19-1.57), P=9.4 × 10(-6) for rs1884613 and OR=1.37 (95%CI 1.20-1.57), P=6.0 × 10(-6) for rs2144908), as previously shown in other populations. We observed body mass index-dependent association of these variants with type 2 diabetes in normal-weight/lean subjects. Variants in USF1, ABCC8, ISL1 and KCNJ11 showed nominal association, while haplotypes in these genes were significantly associated. rs3812704 upstream of NEUROG3 significantly increased risk for type 2 diabetes in normal-weight/lean subjects (OR=1.68 (95%CI 1.25-2.24), P=4.9 × 10(-4)). Thus, pancreatic β-cell development and function genes contribute to susceptibility to type 2 diabetes in North Indians. Variants in genes involved in pancreatic β-cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with complex form. In this study, we studied the genetic association of polymorphisms in such important genes with type 2 diabetes in the high-risk Indians. We genotyped 91 polymorphisms in 19 genes ( ABCC8, HNF1A, HNF1B, HNF4A, INS, INSM1 , ISL1, KCNJ11, MAFA, MNX1, NEUROD1, NEUROG3, NKX2.2, NKX6.1, PAX4, PAX6, PDX1, USF1 and WFS1 ) in 2025 unrelated North Indians of Indo-European ethnicity comprising of 1019 diabetic and 1006 non-diabetic subjects. HNF4A promoter P2 polymorphisms rs1884613 and rs2144908, which are in high linkage disequilibrium, showed significant association with type 2 diabetes (odds ratio (OR)=1.37 (95% confidence interval (CI) 1.19–1.57), P =9.4 × 10 −6 for rs1884613 and OR=1.37 (95%CI 1.20–1.57), P =6.0 × 10 −6 for rs2144908), as previously shown in other populations. We observed body mass index-dependent association of these variants with type 2 diabetes in normal-weight/lean subjects. Variants in USF1 , ABCC8 , ISL1 and KCNJ11 showed nominal association, while haplotypes in these genes were significantly associated. rs3812704 upstream of NEUROG3 significantly increased risk for type 2 diabetes in normal-weight/lean subjects (OR=1.68 (95%CI 1.25–2.24), P =4.9 × 10 −4 ). Thus, pancreatic β-cell development and function genes contribute to susceptibility to type 2 diabetes in North Indians. Variants in genes involved in pancreatic β-cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with complex form. In this study, we studied the genetic association of polymorphisms in such important genes with type 2 diabetes in the high-risk Indians. We genotyped 91 polymorphisms in 19 genes (ABCC8, HNF1A, HNF1B, HNF4A, INS, INSM1, ISL1, KCNJ11, MAFA, MNX1, NEUROD1, NEUROG3, NKX2.2, NKX6.1, PAX4, PAX6, PDX1, USF1 and WFS1) in 2025 unrelated North Indians of Indo-European ethnicity comprising of 1019 diabetic and 1006 non-diabetic subjects. HNF4A promoter P2 polymorphisms rs1884613 and rs2144908, which are in high linkage disequilibrium, showed significant association with type 2 diabetes (odds ratio (OR)=1.37 (95% confidence interval (CI) 1.19–1.57), P=9.4 × 10−6 for rs1884613 and OR=1.37 (95%CI 1.20–1.57), P=6.0 × 10−6 for rs2144908), as previously shown in other populations. We observed body mass index-dependent association of these variants with type 2 diabetes in normal-weight/lean subjects. Variants in USF1, ABCC8, ISL1 and KCNJ11 showed nominal association, while haplotypes in these genes were significantly associated. rs3812704 upstream of NEUROG3 significantly increased risk for type 2 diabetes in normal-weight/lean subjects (OR=1.68 (95%CI 1.25–2.24), P=4.9 × 10−4). Thus, pancreatic β-cell development and function genes contribute to susceptibility to type 2 diabetes in North Indians. Variants in genes involved in pancreatic beta -cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with complex form. In this study, we studied the genetic association of polymorphisms in such important genes with type 2 diabetes in the high-risk Indians. We genotyped 91 polymorphisms in 19 genes (ABCC8, HNF1A, HNF1B, HNF4A, INS, INSM1, ISL1, KCNJ11, MAFA, MNX1, NEUROD1, NEUROG3, NKX2.2, NKX6.1, PAX4, PAX6, PDX1, USF1 and WFS1) in 2025 unrelated North Indians of Indo-European ethnicity comprising of 1019 diabetic and 1006 non-diabetic subjects. HNF4A promoter P2 polymorphisms rs1884613 and rs2144908, which are in high linkage disequilibrium, showed significant association with type 2 diabetes (odds ratio (OR)=1.37 (95% confidence interval (CI) 1.19-1.57), P=9.4 10 super(-6) for rs1884613 and OR=1.37 (95%CI 1.20-1.57), P=6.0 10 super(-6) for rs2144908), as previously shown in other populations. We observed body mass index-dependent association of these variants with type 2 diabetes in normal-weight/lean subjects. Variants in USF1, ABCC8, ISL1 and KCNJ11 showed nominal association, while haplotypes in these genes were significantly associated. rs3812704 upstream of NEUROG3 significantly increased risk for type 2 diabetes in normal-weight/lean subjects (OR=1.68 (95%CI 1.25-2.24), P=4.9 10 super(-4)). Thus, pancreatic beta -cell development and function genes contribute to susceptibility to type 2 diabetes in North Indians. Variants in genes involved in pancreatic β-cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with complex form. In this study, we studied the genetic association of polymorphisms in such important genes with type 2 diabetes in the high-risk Indians. We genotyped 91 polymorphisms in 19 genes (ABCC8, HNF1A, HNF1B, HNF4A, INS, INSM1, ISL1, KCNJ11, MAFA, MNX1, NEUROD1, NEUROG3, NKX2.2, NKX6.1, PAX4, PAX6, PDX1, USF1 and WFS1) in 2025 unrelated North Indians of Indo-European ethnicity comprising of 1019 diabetic and 1006 non-diabetic subjects. HNF4A promoter P2 polymorphisms rs1884613 and rs2144908, which are in high linkage disequilibrium, showed significant association with type 2 diabetes (odds ratio (OR)=1.37 (95% confidence interval (CI) 1.19-1.57), P=9.4 × 10(-6) for rs1884613 and OR=1.37 (95%CI 1.20-1.57), P=6.0 × 10(-6) for rs2144908), as previously shown in other populations. We observed body mass index-dependent association of these variants with type 2 diabetes in normal-weight/lean subjects. Variants in USF1, ABCC8, ISL1 and KCNJ11 showed nominal association, while haplotypes in these genes were significantly associated. rs3812704 upstream of NEUROG3 significantly increased risk for type 2 diabetes in normal-weight/lean subjects (OR=1.68 (95%CI 1.25-2.24), P=4.9 × 10(-4)). Thus, pancreatic β-cell development and function genes contribute to susceptibility to type 2 diabetes in North Indians. |
| Author | Chavali, Sreenivas Tabassum, Rubina Tandon, Nikhil Ghosh, Saurabh Dwivedi, Om Prakash Chauhan, Ganesh Mahajan, Anubha Bharadwaj, Dwaipayan |
| Author_xml | – sequence: 1 givenname: Sreenivas surname: Chavali fullname: Chavali, Sreenivas organization: Genomics and Molecular Medicine Unit, Institute of Genomics and Integrative Biology, CSIR – sequence: 2 givenname: Anubha surname: Mahajan fullname: Mahajan, Anubha organization: Genomics and Molecular Medicine Unit, Institute of Genomics and Integrative Biology, CSIR – sequence: 3 givenname: Rubina surname: Tabassum fullname: Tabassum, Rubina organization: Genomics and Molecular Medicine Unit, Institute of Genomics and Integrative Biology, CSIR – sequence: 4 givenname: Om Prakash surname: Dwivedi fullname: Dwivedi, Om Prakash organization: Genomics and Molecular Medicine Unit, Institute of Genomics and Integrative Biology, CSIR – sequence: 5 givenname: Ganesh surname: Chauhan fullname: Chauhan, Ganesh organization: Genomics and Molecular Medicine Unit, Institute of Genomics and Integrative Biology, CSIR – sequence: 6 givenname: Saurabh surname: Ghosh fullname: Ghosh, Saurabh organization: Human Genetics Unit, Indian Statistical Institute – sequence: 7 givenname: Nikhil surname: Tandon fullname: Tandon, Nikhil email: nikhil_tandon@hotmail.com organization: Department of Endocrinology, All India Institute of Medical Sciences – sequence: 8 givenname: Dwaipayan surname: Bharadwaj fullname: Bharadwaj, Dwaipayan email: db@igib.res.in organization: Genomics and Molecular Medicine Unit, Institute of Genomics and Integrative Biology, CSIR |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21814221$$D View this record in MEDLINE/PubMed |
| BookMark | eNp9kcuKFDEUhoOMOBdduZeACwe02tyqKr0cBi8Dg24U3IV0cqonTXVSJqkeeuND-SDzTKa6W4VBZxFyOPnyc_7_nKIjHzwg9JySGSVcvl3dLGeMUDqT_BE6oYLXFePs29GuFlVNG3qMTlNaEUI4a9kTdMyopIIxeoJ-XKQUjNPZBY9Dhzc6Ou1zws7jJXiYik3oN2CnzqC9iVBgg-9-Vgb6HlvYQB-GNfiMtbe4G73Zid26fIPzdgDMsHV6AXknhj-FWB6ufOn59BQ97nSf4NnhPkNf37_7cvmxuv784ery4royQrS5MnNpdN3UbTmynjcNF8BaApKLjthFbbWxHeF6TmpipdWsbmwHwAQD2_CW8jP0Zq87-kFvb3XfqyG6tY5bRYmaYlQlRjXFqCQv-Ks9PsTwfYSU1dqlya72EMak5oQ0ghIxCZ8_SE4rIKxtZFPQl_fQVRijL7ZVGZQRPidMFurFgRoXa7B_xvy9sgLQPWBiSClCp4zLu_3lqF3_Hz-v7_152P0hrFQov4T4d9B_4b8A8fPGqQ |
| CitedBy_id | crossref_primary_10_1080_14728222_2017_1257000 crossref_primary_10_2337_db23_0604 crossref_primary_10_1155_2014_908152 crossref_primary_10_1155_2015_908152 crossref_primary_10_5567_pharmacologia_2015_149_159 crossref_primary_10_4158_PS_2019_0080 crossref_primary_10_1186_s12881_018_0528_6 crossref_primary_10_1038_srep16247 crossref_primary_10_1089_thy_2022_0144 crossref_primary_10_2174_0118756921327160241022074236 crossref_primary_10_2337_db12_0406 crossref_primary_10_1080_07391102_2023_2233634 crossref_primary_10_1080_07391102_2020_1733666 crossref_primary_10_1007_s12020_012_9844_3 crossref_primary_10_3945_jn_114_203489 crossref_primary_10_4093_dmj_2020_0101 crossref_primary_10_1080_07853890_2022_2138531 crossref_primary_10_2174_0118756921317994240906051408 crossref_primary_10_3390_jpm12020243 crossref_primary_10_1016_j_jsxm_2018_09_012 crossref_primary_10_1038_jhg_2016_80 crossref_primary_10_1002_jcb_28572 crossref_primary_10_1016_j_diabres_2019_107792 crossref_primary_10_7243_2050_0866_2_6 crossref_primary_10_1371_journal_pone_0124662 crossref_primary_10_1371_journal_pone_0117238 crossref_primary_10_1007_s13205_016_0572_x crossref_primary_10_1080_15257770_2021_1905841 crossref_primary_10_2147_PGPM_S329787 crossref_primary_10_1371_journal_pone_0093961 crossref_primary_10_1507_endocrj_EJ12_0325 |
| Cites_doi | 10.2337/db09-1386 10.1210/jc.2008-2754 10.1016/j.molmed.2010.06.004 10.2337/diabetes.53.11.3002 10.1016/j.mrfmmm.2004.07.022 10.1007/s00109-010-0594-5 10.2337/diabetes.54.10.3040 10.2337/diabetes.53.4.1134 10.2337/db08-0719 10.1007/s00125-005-1914-0 10.1016/S0140-6736(03)15268-3 10.1007/s00439-006-0231-0 10.1016/S1262-3636(07)70252-5 10.1056/NEJMra002168 10.2337/db05-1203 10.1093/bioinformatics/bth457 10.1007/s00125-004-1665-3 10.2337/db06-0088 10.2337/diabetes.53.8.2122 10.1007/BF00280883 10.2337/diabetes.54.3.886 10.2337/db06-0178 10.1086/519795 10.2337/diabetes.54.4.1185 10.2337/db07-0513 10.1007/s00125-005-1671-0 10.1002/gepi.10262 10.1007/s10038-008-0335-6 10.2337/diabetes.54.10.3035 10.2337/diacare.27.5.1047 |
| ContentType | Journal Article |
| Copyright | The Japan Society of Human Genetics 2011 The Japan Society of Human Genetics 2011. |
| Copyright_xml | – notice: The Japan Society of Human Genetics 2011 – notice: The Japan Society of Human Genetics 2011. |
| DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7X7 7XB 88E 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 PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS RC3 7X8 ADTOC UNPAY |
| DOI | 10.1038/jhg.2011.83 |
| DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Technology Research Database 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 Central UK/Ireland 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 Health & Medical Complete (Alumni) Biological Sciences ProQuest Health & Medical Collection Medical Database Biological Science Database Biotechnology and BioEngineering Abstracts Proquest Central Premium ProQuest One Academic 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 China Genetics Abstracts MEDLINE - Academic Unpaywall for CDI: Periodical Content Unpaywall |
| DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Central Student Technology Research Database 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 Central China ProQuest Central ProQuest One Applied & Life Sciences ProQuest Health & Medical Research Collection Genetics Abstracts 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 Biological Science Collection ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection 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 One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
| DatabaseTitleList | MEDLINE - Academic ProQuest Central Student Genetics Abstracts MEDLINE |
| 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: UNPAY name: Unpaywall url: https://proxy.k.utb.cz/login?url=https://unpaywall.org/ sourceTypes: Open Access Repository – sequence: 4 dbid: BENPR name: ProQuest Central url: http://www.proquest.com/pqcentral?accountid=15518 sourceTypes: Aggregation Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Biology |
| EISSN | 1435-232X |
| EndPage | 700 |
| ExternalDocumentID | 10.1038/jhg.2011.83 21814221 10_1038_jhg_2011_83 |
| Genre | Research Support, Non-U.S. Gov't Journal Article |
| GroupedDBID | --- -Q- .55 .86 0R~ 1SB 29K 2P1 2VQ 2WC 36B 39C 3O- 3V. 4.4 406 53G 5GY 5VS 6NX 70F 78A 7X7 88E 8FI 8FJ AACDK AAIAL AANZL AASML AATNV AAYZH AAZLF ABAKF ABAWZ ABDBF ABJNI ABUWG ABZZP ACAOD ACBXY ACGFS ACKTT ACOMO ACRQY ACUHS ACZOJ ADBBV ADHDB ADIMF ADINQ AEFQL AEJRE AEMSY AENEX AESKC AEVLU AEXYK AFBBN AFKRA AFLOW AFSHS AGAYW AGHAI AGQEE AHBYD AHMBA AHSBF AIGIU AILAN AJRNO ALFFA ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AMYLF AXYYD AZFZN B0M BAWUL BBNVY BENPR BGNMA BHPHI BKKNO BPHCQ BVXVI CAG CCPQU COF CS3 D-I DIK DL5 DNIVK DPUIP DU5 E3Z EAD EAP EAS EBC EBD EBLON EBS EBX EE. EHN EIOEI EJD EMB EMK EMOBN EPAXT EPL EPT EST ESX F5P FDQFY FEDTE FERAY FIGPU FIZPM FSGXE FYUFA HCIFZ HF~ HG6 HMCUK HVGLF HZ~ I09 IHE IWAJR IXE IZQ JSO JZLTJ KDC KOV KQ8 LAS M1P M4Y M7P NAO NQJWS NU0 O9- OK1 P2P PQQKQ PROAC PSQYO QOK QOS Q~Q RIG RNT RNTTT ROL RPX RRX RSV S1Z S27 SBL SDH SNX SNYQT SOHCF SOJ SRMVM SV3 SWTZT T13 TAOOD TBHMF TDRGL TR2 TSG TSK TUS TWA U2A UKHRP VC2 WJK WK8 X7M ZJWQK ~8M ~KM AAYXX ABBRH ABDBE ABFSG ABRTQ ACSTC AEZWR AFDZB AFHIU AHWEU AIXLP ATHPR AYFIA CITATION PHGZM PHGZT PJZUB PPXIY PQGLB PUEGO CGR CUY CVF ECM EIF NPM 7XB 8FD 8FE 8FH 8FK AZQEC DWQXO FR3 GNUQQ K9. LK8 P64 PKEHL PQEST PQUKI PRINS RC3 7X8 ADTOC UNPAY |
| ID | FETCH-LOGICAL-c447t-c98ca56575658596634e270e834f0db5dacdf03a9050d8da256dfee242ed63713 |
| IEDL.DBID | UNPAY |
| ISSN | 1434-5161 1435-232X |
| IngestDate | Wed Oct 01 16:29:40 EDT 2025 Thu Oct 02 11:37:20 EDT 2025 Thu Oct 02 19:25:52 EDT 2025 Tue Oct 07 06:42:06 EDT 2025 Mon Jul 21 06:05:06 EDT 2025 Wed Oct 01 04:29:50 EDT 2025 Thu Apr 24 22:58:28 EDT 2025 Fri Feb 21 02:36:54 EST 2025 |
| IsDoiOpenAccess | true |
| IsOpenAccess | true |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 10 |
| Keywords | association type 2 diabetes β-cell obesity |
| Language | English |
| License | http://www.springer.com/tdm |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c447t-c98ca56575658596634e270e834f0db5dacdf03a9050d8da256dfee242ed63713 |
| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
| OpenAccessLink | https://proxy.k.utb.cz/login?url=https://www.nature.com/articles/jhg201183.pdf |
| PMID | 21814221 |
| PQID | 2422039028 |
| PQPubID | 2043496 |
| PageCount | 6 |
| ParticipantIDs | unpaywall_primary_10_1038_jhg_2011_83 proquest_miscellaneous_900641041 proquest_miscellaneous_1434027686 proquest_journals_2422039028 pubmed_primary_21814221 crossref_citationtrail_10_1038_jhg_2011_83 crossref_primary_10_1038_jhg_2011_83 springer_journals_10_1038_jhg_2011_83 |
| ProviderPackageCode | CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | 2011-10-01 |
| PublicationDateYYYYMMDD | 2011-10-01 |
| PublicationDate_xml | – month: 10 year: 2011 text: 2011-10-01 day: 01 |
| PublicationDecade | 2010 |
| PublicationPlace | London |
| PublicationPlace_xml | – name: London – name: England |
| PublicationTitle | Journal of human genetics |
| PublicationTitleAbbrev | J Hum Genet |
| PublicationTitleAlternate | J Hum Genet |
| PublicationYear | 2011 |
| Publisher | Nature Publishing Group UK Nature Publishing Group |
| Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group |
| References | AM Bagwell (BFjhg201183_CR19) 2005; 54 T Tanahashi (BFjhg201183_CR26) 2006; 120 S Johansson (BFjhg201183_CR5) 2007; 56 A Bonnefond (BFjhg201183_CR8) 2010; 16 LD Love-Gregory (BFjhg201183_CR20) 2004; 53 SK Hansen (BFjhg201183_CR22) 2005; 48 American Diabetes Association. Expert Committee on the Diagnosis and Classification of Diabetes Mellitus (BFjhg201183_CR10) 2003; 26 W Winckler (BFjhg201183_CR21) 2005; 54 S Wild (BFjhg201183_CR9) 2004; 27 MN Weedon (BFjhg201183_CR29) 2004; 53 DR Matthews (BFjhg201183_CR12) 1985; 28 AE Jackson (BFjhg201183_CR7) 2004; 53 YL Muller (BFjhg201183_CR27) 2005; 54 E Zeggini (BFjhg201183_CR31) 2006; 55 A Mahajan (BFjhg201183_CR11) 2009; 94 WHO Expert Consultation (BFjhg201183_CR18) 2004; 363 F Gibson (BFjhg201183_CR30) 2005; 54 MC Ng (BFjhg201183_CR32) 2005; 48 K Wanic (BFjhg201183_CR28) 2006; 32 R Shen (BFjhg201183_CR13) 2005; 573 S Purcell (BFjhg201183_CR16) 2007; 81 JC Barrett (BFjhg201183_CR15) 2005; 21 M Vaxillaire (BFjhg201183_CR24) 2005; 48 I Barroso (BFjhg201183_CR6) 2008; 57 SS Fajans (BFjhg201183_CR1) 2001; 345 WJ Gauderman (BFjhg201183_CR14) 2003; 25 A Mahajan (BFjhg201183_CR17) 2010; 88 LL Bonnycastle (BFjhg201183_CR23) 2006; 55 G Chauhan (BFjhg201183_CR4) 2010; 59 F Wang (BFjhg201183_CR25) 2009; 122 R Tabassum (BFjhg201183_CR3) 2008; 53 N Yokoi (BFjhg201183_CR2) 2006; 55 |
| References_xml | – volume: 122 start-page: 2477 year: 2009 ident: BFjhg201183_CR25 publication-title: Chin Med J (Engl). – volume: 59 start-page: 2068 year: 2010 ident: BFjhg201183_CR4 publication-title: Diabetes. doi: 10.2337/db09-1386 – volume: 94 start-page: 2123 year: 2009 ident: BFjhg201183_CR11 publication-title: J Clin Endocrinol Metab. doi: 10.1210/jc.2008-2754 – volume: 16 start-page: 407 year: 2010 ident: BFjhg201183_CR8 publication-title: Trends Mol Med. doi: 10.1016/j.molmed.2010.06.004 – volume: 53 start-page: 3002 year: 2004 ident: BFjhg201183_CR29 publication-title: Diabetes. doi: 10.2337/diabetes.53.11.3002 – volume: 573 start-page: 70 year: 2005 ident: BFjhg201183_CR13 publication-title: Mutat Res. doi: 10.1016/j.mrfmmm.2004.07.022 – volume: 88 start-page: 515 year: 2010 ident: BFjhg201183_CR17 publication-title: J Mol Med. doi: 10.1007/s00109-010-0594-5 – volume: 54 start-page: 3040 year: 2005 ident: BFjhg201183_CR30 publication-title: Diabetes. doi: 10.2337/diabetes.54.10.3040 – volume: 53 start-page: 1134 year: 2004 ident: BFjhg201183_CR20 publication-title: Diabetes. doi: 10.2337/diabetes.53.4.1134 – volume: 57 start-page: 3161 year: 2008 ident: BFjhg201183_CR6 publication-title: Diabetes. doi: 10.2337/db08-0719 – volume: 48 start-page: 2018 year: 2005 ident: BFjhg201183_CR32 publication-title: Diabetologia. doi: 10.1007/s00125-005-1914-0 – volume: 363 start-page: 157 year: 2004 ident: BFjhg201183_CR18 publication-title: Lancet doi: 10.1016/S0140-6736(03)15268-3 – volume: 120 start-page: 527 year: 2006 ident: BFjhg201183_CR26 publication-title: Hum Genet. doi: 10.1007/s00439-006-0231-0 – volume: 32 start-page: 86 year: 2006 ident: BFjhg201183_CR28 publication-title: Diabetes Metab. doi: 10.1016/S1262-3636(07)70252-5 – volume: 345 start-page: 971 year: 2001 ident: BFjhg201183_CR1 publication-title: N Engl J Med. doi: 10.1056/NEJMra002168 – volume: 55 start-page: 2379 year: 2006 ident: BFjhg201183_CR2 publication-title: Diabetes. doi: 10.2337/db05-1203 – volume: 21 start-page: 263 year: 2005 ident: BFjhg201183_CR15 publication-title: Bioinformatics. doi: 10.1093/bioinformatics/bth457 – volume: 48 start-page: 440 year: 2005 ident: BFjhg201183_CR24 publication-title: Diabetologia. doi: 10.1007/s00125-004-1665-3 – volume: 55 start-page: 2541 year: 2006 ident: BFjhg201183_CR31 publication-title: Diabetes. doi: 10.2337/db06-0088 – volume: 53 start-page: 2122 year: 2004 ident: BFjhg201183_CR7 publication-title: Diabetes. doi: 10.2337/diabetes.53.8.2122 – volume: 26 start-page: S5 issue: Suppl 1 year: 2003 ident: BFjhg201183_CR10 publication-title: Diabetes Care. – volume: 28 start-page: 412 year: 1985 ident: BFjhg201183_CR12 publication-title: Diabetologia. doi: 10.1007/BF00280883 – volume: 54 start-page: 886 year: 2005 ident: BFjhg201183_CR21 publication-title: Diabetes. doi: 10.2337/diabetes.54.3.886 – volume: 55 start-page: 2534 year: 2006 ident: BFjhg201183_CR23 publication-title: Diabetes. doi: 10.2337/db06-0178 – volume: 81 start-page: 559 year: 2007 ident: BFjhg201183_CR16 publication-title: Am J Hum Genet. doi: 10.1086/519795 – volume: 54 start-page: 1185 year: 2005 ident: BFjhg201183_CR19 publication-title: Diabetes. doi: 10.2337/diabetes.54.4.1185 – volume: 56 start-page: 3112 year: 2007 ident: BFjhg201183_CR5 publication-title: Diabetes. doi: 10.2337/db07-0513 – volume: 48 start-page: 452 year: 2005 ident: BFjhg201183_CR22 publication-title: Diabetologia. doi: 10.1007/s00125-005-1671-0 – volume: 25 start-page: 327 year: 2003 ident: BFjhg201183_CR14 publication-title: Genet Epidemiol. doi: 10.1002/gepi.10262 – volume: 53 start-page: 957 year: 2008 ident: BFjhg201183_CR3 publication-title: J Hum Genet. doi: 10.1007/s10038-008-0335-6 – volume: 54 start-page: 3035 year: 2005 ident: BFjhg201183_CR27 publication-title: Diabetes. doi: 10.2337/diabetes.54.10.3035 – volume: 27 start-page: 1047 year: 2004 ident: BFjhg201183_CR9 publication-title: Diabetes Care. doi: 10.2337/diacare.27.5.1047 |
| SSID | ssj0003272 |
| Score | 2.126825 |
| Snippet | Variants in genes involved in pancreatic β-cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with... Variants in genes involved in pancreatic beta -cell development and function are known to cause monogenic forms of type 2 diabetes and are also associated with... |
| SourceID | unpaywall proquest pubmed crossref springer |
| SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 695 |
| SubjectTerms | 631/208/726/649 631/208/727/2000 692/699/2743/137/773 Basic Helix-Loop-Helix Transcription Factors - genetics Basic Helix-Loop-Helix Transcription Factors - metabolism Beta cells Beta2 protein Biomedical and Life Sciences Biomedicine Body Mass Index Case-Control Studies Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - ethnology Diabetes Mellitus, Type 2 - genetics Gene Expression Gene Function Gene Therapy Genetic Predisposition to Disease Genetic Variation Genotype Haplotypes Hepatocyte nuclear factor 4 Hepatocyte Nuclear Factor 4 - genetics Hepatocyte Nuclear Factor 4 - metabolism Human Genetics Humans Indians, North American - genetics Insulin-Secreting Cells - cytology Insulin-Secreting Cells - physiology Islet-1 protein Linkage disequilibrium Molecular Medicine Nerve Tissue Proteins - genetics Nerve Tissue Proteins - metabolism Nkx2.2 protein Nkx6.1 protein Obesity original-article Pancreas Pax6 protein Polymorphism, Single Nucleotide |
| SummonAdditionalLinks | – databaseName: ProQuest Central dbid: BENPR link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1fa9RAEB_qFdE-SKtWo62sYF-E0CS7m-w9FFFpqUIPEQt9C5v901aO3OndtfTFD-UH8TN1JsneXWntQyAky2az-9vZ38zszgC8M14oaVEtEZUjN6PEOeecjgspUSIXVV40ITaOBvnhsfh6Ik9WYBDOwtC2yiATG0FtR4Zs5Lu4lGQJp1gjH8a_YsoaRd7VkEJDd6kV7F4TYuwBrGYUGasHq5_2B9--z2Uzz5p0TkgSRCyR7HQn9hKudn-enbYRPRW_uUbdIp5LTtM1eDSrx_rqUg-HS-vSwTo86Qgl-9giYANWXP0UHrYpJq-ewZ-l_mcjzy5QN6atL-y8Zqck5_AGJdSFs_QERUPLIg379zcmoz6zi11FTNeW0ULYVEYWXEYWXJaxYMGlOhpPEPtSE_Amz-H4YP_H58O4y7kQGyGKaWz6ymhyheKlJOpCXLisSJziwie2klYb6xOu-4lMrLIaGZP1zuHoOJtz1Hg3oVePavcSmNOoCuVeFMahzqVMlfoq91nqvUu9yVUE70Mvl6YLSE55MYZl4xjnqsQhKWlISsUjhFUoPG7jcNxdbCsMV9lNxkm5gE4Eb-evcRpRN-rajWaTkhCBGnqu8gjYf8r0ib-h-ppG8KJFwrwpRJTwK_hmJ0Bj8f0727kzx819__Pq_v95DY-zsCcx3YLe9PfMbSNJmlZvOuRfA6nWEZA priority: 102 providerName: ProQuest |
| Title | Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians |
| URI | https://link.springer.com/article/10.1038/jhg.2011.83 https://www.ncbi.nlm.nih.gov/pubmed/21814221 https://www.proquest.com/docview/2422039028 https://www.proquest.com/docview/1434027686 https://www.proquest.com/docview/900641041 https://www.nature.com/articles/jhg201183.pdf |
| UnpaywallVersion | publishedVersion |
| Volume | 56 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| journalDatabaseRights | – providerCode: PRVEBS databaseName: EBSCOhost Academic Search Ultimate customDbUrl: https://search.ebscohost.com/login.aspx?authtype=ip,shib&custid=s3936755&profile=ehost&defaultdb=asn eissn: 1435-232X dateEnd: 20151031 omitProxy: true ssIdentifier: ssj0003272 issn: 1435-232X databaseCode: ABDBF dateStart: 19980101 isFulltext: true titleUrlDefault: https://search.ebscohost.com/direct.asp?db=asn providerName: EBSCOhost – providerCode: PRVBFR databaseName: Free Medical Journals - Free Access to All customDbUrl: eissn: 1435-232X dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0003272 issn: 1435-232X databaseCode: DIK dateStart: 19770101 isFulltext: true titleUrlDefault: http://www.freemedicaljournals.com providerName: Flying Publisher – providerCode: PRVLSH databaseName: SpringerLink Journals customDbUrl: mediaType: online eissn: 1435-232X dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0003272 issn: 1435-232X databaseCode: AFBBN dateStart: 19970301 isFulltext: true providerName: Library Specific Holdings – providerCode: PRVPQU databaseName: ProQuest Central customDbUrl: http://www.proquest.com/pqcentral?accountid=15518 eissn: 1435-232X dateEnd: 20171231 omitProxy: true ssIdentifier: ssj0003272 issn: 1435-232X databaseCode: BENPR dateStart: 20000101 isFulltext: true titleUrlDefault: https://www.proquest.com/central providerName: ProQuest – providerCode: PRVPQU databaseName: ProQuest Health & Medical Collection customDbUrl: eissn: 1435-232X dateEnd: 20171231 omitProxy: true ssIdentifier: ssj0003272 issn: 1435-232X databaseCode: 7X7 dateStart: 20000101 isFulltext: true titleUrlDefault: https://search.proquest.com/healthcomplete providerName: ProQuest |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwEB7RXSHgwPsRKCsj0QtSShI7jvdYUKuCxKpCrLScIsePQrvKVuxuUTnwo_gh_CZm4mS7QEE9RIriiZ_j8Tee8RjgufFC5RbVElE5MjPmOOec03GR5yiRi0oWTYiNdyO5PxZvJ_mkPaw-b90qQ0jLRkx33mEvjz4d0lKlUPOzfgP6Mkfo3YP-eHSw87E5QcRFnKchPipCgBiRwqQ9j5dwRf-HeJ2K_74C_QUr10yiN-Dasj7RZ1_1dLq26uzdglFX3-Bscry9XFTb5tsfoRwv3aDbcLPFn2wnENyBK66-C1fDjZRn9-D72nCxmWenqEqTpwz7XLNDEov4ggLt1Fn6gpIkgE7Dfv6IyQbA7LkTEtO1ZbRuNpnRhi-jDV-WsW7Dl_JoDEfsTU18Or8P473dD6_34_aKhtgIUSxiM1RGk-UUH4VDIrlwWZE4xYVPbJVbbaxPuB4meWKV1QiwrHcOcYGzkqOC_AB69ax2j4A5jZqT9KIwDlU0ZarUV9Jnqfcu9UaqCF50w1aaNn45XaMxLRs7OlcldmlJfVoqHiEXdsQnIWzHxWSb3fiX7dydl1i5LOEU1SaCZ6tknHXUjbp2s-W8JHZDhV4qGQH7B82Q4B5qu2kEDwNrrapCuApLwZStjtfOy7-wnlsrRvxfex5fku4JXM86X8Z0E3qLL0v3FMHVohrARjEpBtB_tTs6eD9oJ9gvlUcnhQ |
| linkProvider | Unpaywall |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LT9tAEB5RUEV7qPrGlLZbqblUsrC9a3tzQFUfoKRAVFUgcTPrfVBQ5IQmAeXCj-oP6E_ob-qMH0mqUm4cLFn2ar3eeX2zszsD8FY7IWODbonILYUZY5Q5a5WfxjFq5DRP0jLFxn4v6RyKL0fx0RL8as7C0LbKRieWitoMNK2Rb6IpiQJOuUbeD899qhpF0dWmhIaqSyuYrTLFWH2wY9dOL9GFG211PyO9W1G0s33wqePXVQZ8LUQ69nVbakXBP7xkjOifCxulgZVcuMDksVHauICrdhAHRhqFGME4a3E81iQcfTzs9w6sCC7a6PytfNzuff02swU8KstHISgRfozgqj4hGHC5efb9pMogKvnfNvEfoLsQpL0Pq5NiqKaXqt9fsIM7D-FBDWDZh4rjHsGSLR7D3aqk5fQJXC3Qmw0cu0BfnLbasNOCnZBexRvUiBfW0BNURRVq1ez3T5-CCMzMdzExVRhGhrfsjFaMGa0Ys4g1K8bURxl5Yt2CGH30FA5vZfafwXIxKOwaMKvQ9UqcSLVFH0_qPHR54qLQORs6nUgP3jWznOk6ATrV4ehnZSCeywxJkhFJMsk9ZOOm8bDK-3F9s42GXFkt_KNszqoevJm9RrGlaVSFHUxGGXFEEKGvl3jA_tOmTXgR3eXQg-cVJ8yGQsAMv4JvWg1rzL9_7ThbM7656X_Wb_6f17DaOdjfy_a6vd0XcC9q9kOGG7A8_jGxLxGgjfNXtRQwOL5twfsDU7BOEA |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEB6VIigcEK-CS4FFIhckK7Z3bW8OCCFK1FCoOFApN7PeRwFFTiBJq1z4UT3yI_hNzNjeJIjSWw-WLHu13t157Dc74xmA59oJmRo0S0Rpyc2YosxZq8I8TVEj52WW1yk2Phxm-0fi3TAdbsAv_y8MhVV6nVgrajPWdEbexa0kiTjlGum6Nizi417_1eR7SBWkyNPqy2k0LHJgF6dovk1fDvaQ1p0k6b_99GY_bCsMhFqIfBbqntSKHH94yRSRPxc2ySMruXCRKVOjtHERV70ojYw0CvGBcdbiWKzJONp32O8VuJpz3qNwwny4NPYintSFoxCOiDBFWNX-Gxhx2f325bjJHSr537vhPxB3zT17E7bm1UQtTtVotLYD9m_DrRa6stcNr92BDVvdhWtNMcvFPfi5Rmk2duwErXAKsmFfK3ZMGhVvUBeeWENPUAk1eFWz32chuQ-YWcUvMVUZRltu3RmdFTM6K2YJ82fF1Eftc2KDilh8eh-OLmXtt2GzGlf2ITCr0OjKnMi1RetO6jJ2ZeaS2DkbO53JAF74VS50m_qcKnCMitoFz2WBJCmIJIXkATKwbzxpMn6c32zXk6toxX5arJg0gGfL1yiwtIyqsuP5tCCOiBK08rIA2H_a9AgpoqEcB_Cg4YTlUAiS4VfwTcezxur7546zs-Sbi-azc_F8nsJ1FLfi_eDw4BHcSHwgZLwLm7Mfc_sYkdmsfFKLAIPPly1zfwAvokuq |
| linkToUnpaywall | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwEB7BVgh64FkgUJCR6AUpbRI_4j1WiKogseLASsspcvwoj1W2YneL2gM_ih_Cb2ImTrYLFNRDpCie-Dkef-MZjwGe2yC0dKiWiNqTmVHinPPepKWUKJHLWpVtiI23I3U4Fm8mctIdVp93bpUxpGUrpnvvsL3PH49oqdKo-blwFTaUROg9gI3x6N3-h_YEERepzGN8VIQAKSKFSXceL-Oa_o_xOjX_fQX6C1aumUQ34fqyOTan38x0urbqHNyCUV_f6GzyZXe5qHft2R-hHC_doNtws8OfbD8S3IErvrkL1-KNlKf34PvacLFZYCeoSpOnDPvUsCMSi_iCAu3EO_qCkiSCTst-_kjJBsDcuRMSM41jtG62mdGGL6MNX1awfsOX8mgNR-x1Q3w634Lxwav3Lw_T7oqG1ApRLlI71NaQ5RQfjUOiuPBFmXnNRchcLZ2xLmTcDDOZOe0MAiwXvEdc4J3iqCDfh0Eza_xDYN6g5qSCKK1HFU3bOg-1CkUegs-DVTqBF_2wVbaLX07XaEyr1o7OdYVdWlGfVponyIU98XEM23Ex2XY__lU3d-cVVq7IOEW1SeDZKhlnHXWjafxsOa-I3VChV1olwP5BMyS4h9punsCDyFqrqhCuwlIwZafntfPyL6znzooR_9eeR5ekeww3it6XMd-GweLr0j9BcLWon3ZT6heDvSUE |
| 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=Association+of+variants+in+genes+involved+in+pancreatic+%CE%B2-cell+development+and+function+with+type+2+diabetes+in+North+Indians&rft.jtitle=Journal+of+human+genetics&rft.au=Chavali%2C+Sreenivas&rft.au=Mahajan%2C+Anubha&rft.au=Tabassum%2C+Rubina&rft.au=Dwivedi%2C+Om+Prakash&rft.date=2011-10-01&rft.eissn=1435-232X&rft.volume=56&rft.issue=10&rft.spage=695&rft_id=info:doi/10.1038%2Fjhg.2011.83&rft_id=info%3Apmid%2F21814221&rft.externalDocID=21814221 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1434-5161&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1434-5161&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1434-5161&client=summon |