138 related articles for article (PubMed ID: 35796342)
21. Alterations in bile acid synthesis in carriers of hepatocyte nuclear factor 1α mutations.
Ekholm E; Nilsson R; Groop L; Pramfalk C
J Intern Med; 2013 Sep; 274(3):263-72. PubMed ID: 23607861
[TBL] [Abstract][Full Text] [Related]
22. Human insulin gene is a target gene of hepatocyte nuclear factor-1alpha (HNF-1alpha) and HNF-1beta.
Okita K; Yang Q; Yamagata K; Hangenfeldt KA; Miyagawa J; Kajimoto Y; Nakajima H; Namba M; Wollheim CB; Hanafusa T; Matsuzawa Y
Biochem Biophys Res Commun; 1999 Sep; 263(2):566-9. PubMed ID: 10491332
[TBL] [Abstract][Full Text] [Related]
23. HNF1A:From Monogenic Diabetes to Type 2 Diabetes and Gestational Diabetes Mellitus.
Li LM; Jiang BG; Sun LL
Front Endocrinol (Lausanne); 2022; 13():829565. PubMed ID: 35299962
[TBL] [Abstract][Full Text] [Related]
24. Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families.
Costa A; Bescós M; Velho G; Chêvre J; Vidal J; Sesmilo G; Bellanné-Chantelot C; Froguel P; Casamitjana R; Rivera-Fillat F; Gomis R; Conget I
Eur J Endocrinol; 2000 Apr; 142(4):380-6. PubMed ID: 10754480
[TBL] [Abstract][Full Text] [Related]
25. Structure-function studies of HNF1A (MODY3) gene mutations in South Indian patients with monogenic diabetes.
Balamurugan K; Bjørkhaug L; Mahajan S; Kanthimathi S; Njølstad PR; Srinivasan N; Mohan V; Radha V
Clin Genet; 2016 Dec; 90(6):486-495. PubMed ID: 26853433
[TBL] [Abstract][Full Text] [Related]
26. Novel mutations and a mutational hotspot in the MODY3 gene.
Glucksmann MA; Lehto M; Tayber O; Scotti S; Berkemeier L; Pulido JC; Wu Y; Nir WJ; Fang L; Markel P; Munnelly KD; Goranson J; Orho M; Young BM; Whitacre JL; McMenimen C; Wantman M; Tuomi T; Warram J; Forsblom CM; Carlsson M; Rosenzweig J; Kennedy G; Duyk GM; Thomas JD
Diabetes; 1997 Jun; 46(6):1081-6. PubMed ID: 9166684
[TBL] [Abstract][Full Text] [Related]
27. Monogenic diabetes mellitus in youth. The MODY syndromes.
Winter WE; Nakamura M; House DV
Endocrinol Metab Clin North Am; 1999 Dec; 28(4):765-85. PubMed ID: 10609119
[TBL] [Abstract][Full Text] [Related]
28. Two case reports of maturity-onset diabetes of the young type 3 caused by the hepatocyte nuclear factor 1α gene mutation.
Wen Q; Li Y; Shao H; Ma J; Lin Y; Sun Y; Liu T
Open Med (Wars); 2023; 18(1):20230705. PubMed ID: 37197360
[TBL] [Abstract][Full Text] [Related]
29. Clinical characteristics and diagnostic criteria of maturity-onset diabetes of the young (MODY) due to molecular anomalies of the HNF1A gene.
Bellanné-Chantelot C; Lévy DJ; Carette C; Saint-Martin C; Riveline JP; Larger E; Valéro R; Gautier JF; Reznik Y; Sola A; Hartemann A; Laboureau-Soares S; Laloi-Michelin M; Lecomte P; Chaillous L; Dubois-Laforgue D; Timsit J;
J Clin Endocrinol Metab; 2011 Aug; 96(8):E1346-51. PubMed ID: 21677039
[TBL] [Abstract][Full Text] [Related]
30. Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations.
Vaxillaire M; Abderrahmani A; Boutin P; Bailleul B; Froguel P; Yaniv M; Pontoglio M
J Biol Chem; 1999 Dec; 274(50):35639-46. PubMed ID: 10585442
[TBL] [Abstract][Full Text] [Related]
31. Decreased glibenclamide uptake in hepatocytes of hepatocyte nuclear factor-1alpha-deficient mice: a mechanism for hypersensitivity to sulfonylurea therapy in patients with maturity-onset diabetes of the young, type 3 (MODY3).
Boileau P; Wolfrum C; Shih DQ; Yang TA; Wolkoff AW; Stoffel M
Diabetes; 2002 Dec; 51 Suppl 3():S343-8. PubMed ID: 12475773
[TBL] [Abstract][Full Text] [Related]
32. [A Dutch family with an autosomal dominant form of diabetes mellitus as a result of a mutation in the HNF1 alpha-gene (MODY3)].
Tack CJ; Hattersley AT
Ned Tijdschr Geneeskd; 1998 Oct; 142(41):2252-6. PubMed ID: 9864503
[TBL] [Abstract][Full Text] [Related]
33. [Hepatocyte nuclear factor 1α-inactivated hepatocellular adenomatosis in a patient with maturity-onset diabetes of the young type 3: case report and literature review].
Hirata E; Shimizu S; Umeda S; Kobayashi T; Nakano M; Higuchi H; Serizawa H; Iwasaki N; Morinaga S; Tsunematsu S
Nihon Shokakibyo Gakkai Zasshi; 2015; 112(9):1696-704. PubMed ID: 26346360
[TBL] [Abstract][Full Text] [Related]
34. Identification of a new mutation in the hepatocyte nuclear factor-1alpha gene in a Polish family with early-onset type 2 diabetes mellitus.
Malecki MT; Klupa T; Frey J; Cyganek K; Galicka-Stankowska D; Wanic K; Sieradzki J
Diabetes Nutr Metab; 2001 Oct; 14(5):288-91. PubMed ID: 11806470
[TBL] [Abstract][Full Text] [Related]
35. Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q.
Shaw JT; Lovelock PK; Kesting JB; Cardinal J; Duffy D; Wainwright B; Cameron DP
Diabetes; 1998 Nov; 47(11):1793-6. PubMed ID: 9792550
[TBL] [Abstract][Full Text] [Related]
36. Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect.
Klupa T; Warram JH; Antonellis A; Pezzolesi M; Nam M; Malecki MT; Doria A; Rich SS; Krolewski AS
Diabetes Care; 2002 Dec; 25(12):2292-301. PubMed ID: 12453976
[TBL] [Abstract][Full Text] [Related]
37. Identification and functional characterization of a novel mutation of hepatocyte nuclear factor-1alpha gene in a Korean family with MODY3.
Kim KA; Kang K; Chi YI; Chang I; Lee MK; Kim KW; Shoelson SE; Lee MS
Diabetologia; 2003 May; 46(5):721-7. PubMed ID: 12712243
[TBL] [Abstract][Full Text] [Related]
38. Genetic variation in the hepatocyte nuclear factor-1 alpha gene in Danish Caucasians with late-onset NIDDM.
Urhammer SA; Rasmussen SK; Kaisaki PJ; Oda N; Yamagata K; Møller AM; Fridberg M; Hansen L; Hansen T; Bell GI; Pedersen O
Diabetologia; 1997 Apr; 40(4):473-5. PubMed ID: 9112026
[TBL] [Abstract][Full Text] [Related]
39. Structure/function studies of hepatocyte nuclear factor-1alpha, a diabetes-associated transcription factor.
Yang Q; Yamagata K; Yamamoto K; Miyagawa J; Takeda J; Iwasaki N; Iwahashi H; Yoshiuchi I; Namba M; Miyazaki J; Hanafusa T; Matsuzawa Y
Biochem Biophys Res Commun; 1999 Dec; 266(1):196-202. PubMed ID: 10581189
[TBL] [Abstract][Full Text] [Related]
40. Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
Low BSJ; Lim CS; Ding SSL; Tan YS; Ng NHJ; Krishnan VG; Ang SF; Neo CWY; Verma CS; Hoon S; Lim SC; Tai ES; Teo AKK
Nat Commun; 2021 May; 12(1):3133. PubMed ID: 34035238
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]