224 related articles for article (PubMed ID: 17426099)
21. Causal variants in Maturity Onset Diabetes of the Young (MODY) - A systematic review.
Rafique I; Mir A; Saqib MAN; Naeem M; Marchand L; Polychronakos C
BMC Endocr Disord; 2021 Nov; 21(1):223. PubMed ID: 34763692
[TBL] [Abstract][Full Text] [Related]
22. PAX4 gene variations predispose to ketosis-prone diabetes.
Mauvais-Jarvis F; Smith SB; Le May C; Leal SM; Gautier JF; Molokhia M; Riveline JP; Rajan AS; Kevorkian JP; Zhang S; Vexiau P; German MS; Vaisse C
Hum Mol Genet; 2004 Dec; 13(24):3151-9. PubMed ID: 15509590
[TBL] [Abstract][Full Text] [Related]
23. Novel
Lee YL; Ting TH; Lim CT; Arrumugam-Arthini C; Karuppiah T; Ling KH
J Pediatr Endocrinol Metab; 2023 Oct; 36(10):988-992. PubMed ID: 37621150
[TBL] [Abstract][Full Text] [Related]
24. Nonsynonymous Variants in
Kwak SH; Chae J; Lee S; Choi S; Koo BK; Yoon JW; Park JH; Cho B; Moon MK; Lim S; Cho YM; Moon S; Kim YJ; Han S; Hwang MY; Cho YS; Lee MS; Jang HC; Kang HM; Park T; Cho NH; Kim K; Kim JI; Park KS
Diabetes; 2018 Sep; 67(9):1892-1902. PubMed ID: 29941447
[TBL] [Abstract][Full Text] [Related]
25. Association of novel variants in the hepatocyte nuclear factor 4A gene with maturity onset diabetes of the young and early onset type 2 diabetes.
Anuradha S; Radha V; Mohan V
Clin Genet; 2011 Dec; 80(6):541-9. PubMed ID: 21062274
[TBL] [Abstract][Full Text] [Related]
26. Beta-cell dysfunction in late-onset diabetic subjects carrying homozygous mutation in transcription factors NeuroD1 and Pax4.
Kanatsuka A; Tokuyama Y; Nozaki O; Matsui K; Egashira T
Metabolism; 2002 Sep; 51(9):1161-5. PubMed ID: 12200761
[TBL] [Abstract][Full Text] [Related]
27. [Alternative Variants of Pax4 Human Transcription Factor: Comparative Transcriptional Activity].
Melnikova AI; Krasnova TS; Zubkova NA; Tiulpakov AN; Rubtsov PM
Mol Biol (Mosk); 2020; 54(5):849-857. PubMed ID: 33009794
[TBL] [Abstract][Full Text] [Related]
28. [Association between A1168C polymorphism in PAX4 gene and type 1 diabetes in Han Chinese].
Zhang Y; Xiao XH; Wang H; Wang T; Sun Q; Yang GH; Fu Y; Yuan T; Zhang Q; Liu QY
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2007 Jun; 29(3):370-3. PubMed ID: 17633464
[TBL] [Abstract][Full Text] [Related]
29. Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.
Ma RC; Hu C; Tam CH; Zhang R; Kwan P; Leung TF; Thomas GN; Go MJ; Hara K; Sim X; Ho JS; Wang C; Li H; Lu L; Wang Y; Li JW; Wang Y; Lam VK; Wang J; Yu W; Kim YJ; Ng DP; Fujita H; Panoutsopoulou K; Day-Williams AG; Lee HM; Ng AC; Fang YJ; Kong AP; Jiang F; Ma X; Hou X; Tang S; Lu J; Yamauchi T; Tsui SK; Woo J; Leung PC; Zhang X; Tang NL; Sy HY; Liu J; Wong TY; Lee JY; Maeda S; Xu G; Cherny SS; Chan TF; Ng MC; Xiang K; Morris AP; ; Keildson S; ; Hu R; Ji L; Lin X; Cho YS; Kadowaki T; Tai ES; Zeggini E; McCarthy MI; Hon KL; Baum L; Tomlinson B; So WY; Bao Y; Chan JC; Jia W
Diabetologia; 2013 Jun; 56(6):1291-305. PubMed ID: 23532257
[TBL] [Abstract][Full Text] [Related]
30. Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing.
Shim YJ; Kim JE; Hwang SK; Choi BS; Choi BH; Cho EM; Jang KM; Ko CW
Horm Res Paediatr; 2015; 83(4):242-51. PubMed ID: 25765181
[TBL] [Abstract][Full Text] [Related]
31. A three-step programmed method for the identification of causative gene mutations of maturity onset diabetes of the young (MODY).
Li Q; Cao X; Qiu HY; Lu J; Gao R; Liu C; Yuan MX; Yang GR; Yang JK
Gene; 2016 Aug; 588(2):141-8. PubMed ID: 27185633
[TBL] [Abstract][Full Text] [Related]
32. High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes.
Lehto M; Wipemo C; Ivarsson SA; Lindgren C; Lipsanen-Nyman M; Weng J; Wibell L; Widén E; Tuomi T; Groop L
Diabetologia; 1999 Sep; 42(9):1131-7. PubMed ID: 10447526
[TBL] [Abstract][Full Text] [Related]
33. Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes.
Ming-Qiang Z; Yang-Li D; Ke H; Wei W; Jun-Fen F; Chao-Chun Z; Guan-Ping D
J Pediatr Endocrinol Metab; 2019 Jul; 32(7):759-765. PubMed ID: 31216263
[TBL] [Abstract][Full Text] [Related]
34. Asian MODY: are we missing an important diagnosis?
Porter JR; Rangasami JJ; Ellard S; Gloyn AL; Shields BM; Edwards J; Anderson JM; Shaw NJ; Hattersley AT; Frayling TM; Plunkett M; Barrett TG
Diabet Med; 2006 Nov; 23(11):1257-60. PubMed ID: 17054605
[TBL] [Abstract][Full Text] [Related]
35. Mutation screening of the hepatocyte nuclear factor (HNF)-6 gene in Japanese subjects with diabetes mellitus.
Zhu Q; Yamagata K; Tsukahara Y; Yang Q; Liu W; Hanafusa T; Miyagawa J; Matsuzawa Y
Diabetes Res Clin Pract; 2001 Jun; 52(3):171-4. PubMed ID: 11323086
[TBL] [Abstract][Full Text] [Related]
36. Association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity.
Biason-Lauber A; Boehm B; Lang-Muritano M; Gauthier BR; Brun T; Wollheim CB; Schoenle EJ
Diabetologia; 2005 May; 48(5):900-5. PubMed ID: 15834548
[TBL] [Abstract][Full Text] [Related]
37. The association of the PAX4 gene with type 1 diabetes in Han Chinese.
Zhang Y; Xiao X; Liu Y; Zhu X; Wenhui L; Li N; Yuan T; Wang H
Diabetes Res Clin Pract; 2008 Sep; 81(3):365-9. PubMed ID: 18617287
[TBL] [Abstract][Full Text] [Related]
38. Linkage and molecular scanning analyses of MODY3/hepatocyte nuclear factor-1 alpha gene in typical familial type 2 diabetes: evidence for novel mutations in exons 8 and 10.
Elbein SC; Teng K; Yount P; Scroggin E
J Clin Endocrinol Metab; 1998 Jun; 83(6):2059-65. PubMed ID: 9626139
[TBL] [Abstract][Full Text] [Related]
39. Hepatocyte nuclear factor-6: associations between genetic variability and type II diabetes and between genetic variability and estimates of insulin secretion.
Møller AM; Ek J; Durviaux SM; Urhammer SA; Clausen JO; Eiberg H; Hansen T; Rousseau GG; Lemaigre FP; Pedersen O
Diabetologia; 1999 Aug; 42(8):1011-6. PubMed ID: 10491763
[TBL] [Abstract][Full Text] [Related]
40. C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review.
Zhang D; Chen C; Yang W; Piao Y; Ren L; Sang Y
Medicine (Baltimore); 2022 Dec; 101(51):e32461. PubMed ID: 36595822
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
