Literature DB >> 9648841

Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.

F Beards1, T Frayling, M Bulman, Y Horikawa, L Allen, M Appleton, G I Bell, S Ellard, A T Hattersley.   

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Year:  1998        PMID： 9648841     DOI： 10.2337/diabetes.47.7.1152

Source DB:  PubMed          Journal:  Diabetes        ISSN： 0012-1797            Impact factor:   9.461


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  14 in total

Review 1.  Hepatocyte Nuclear Factor 1β-Associated Kidney Disease: More than Renal Cysts and Diabetes.

Authors:  Jacobien C Verhave; Anneke P Bech; Jack F M Wetzels; Tom Nijenhuis
Journal:  J Am Soc Nephrol       Date:  2015-08-28       Impact factor: 10.121

2.  Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes.

Authors:  Limei Liu; Kazuaki Nagashima; Takao Yasuda; Yanjun Liu; Hai-Rong Hu; Guang He; Bo Feng; Mingming Zhao; Langen Zhuang; Taishan Zheng; Theodore C Friedman; Kunsan Xiang
Journal:  Diabetologia       Date:  2013-09-10       Impact factor: 10.122

3.  Genetic Counseling for Diabetes Mellitus.

Authors:  Stephanie A Stein; Kristin L Maloney; Toni I Pollin
Journal:  Curr Genet Med Rep       Date:  2014-06-01

4.  Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes.

Authors:  W M Macfarlane; T M Frayling; S Ellard; J C Evans; L I Allen; M P Bulman; S Ayres; M Shepherd; P Clark; A Millward; A Demaine; T Wilkin; K Docherty; A T Hattersley
Journal:  J Clin Invest       Date:  1999-11       Impact factor: 14.808

Review 5.  Hepatic phenotypes of HNF1B gene mutations: a case of neonatal cholestasis requiring portoenterostomy and literature review.

Authors:  Radana Kotalova; Petra Dusatkova; Ondrej Cinek; Lenka Dusatkova; Tomas Dedic; Tomas Seeman; Jan Lebl; Stepanka Pruhova
Journal:  World J Gastroenterol       Date:  2015-02-28       Impact factor: 5.742

6.  Mutations in hepatocyte nuclear factor-1beta and their related phenotypes.

Authors:  E L Edghill; C Bingham; S Ellard; A T Hattersley
Journal:  J Med Genet       Date:  2005-06-01       Impact factor: 6.318

7.  HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.

Authors:  Makiko Nakayama; Kandai Nozu; Yuki Goto; Koichi Kamei; Shuichi Ito; Hidenori Sato; Mitsuru Emi; Koichi Nakanishi; Shigeru Tsuchiya; Kazumoto Iijima
Journal:  Pediatr Nephrol       Date:  2010-02-13       Impact factor: 3.714

8.  Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease.

Authors:  C Bingham; M P Bulman; S Ellard; L I Allen; G W Lipkin; W G Hoff; A S Woolf; G Rizzoni; G Novelli; A J Nicholls; A T Hattersley
Journal:  Am J Hum Genet       Date:  2000-11-20       Impact factor: 11.025

9.  A novel mutation, Ser159Pro in the NeuroD1/BETA2 gene contributes to the development of diabetes in a Chinese potential MODY family.

Authors:  Limei Liu; Hiroto Furuta; Asako Minami; Taishan Zheng; Weiping Jia; Kishio Nanjo; Kunsan Xiang
Journal:  Mol Cell Biochem       Date:  2007-04-18       Impact factor: 3.396

10.  Cost-effective PKHD1 genetic testing for autosomal recessive polycystic kidney disease.

Authors:  Paola Krall; Cristina Pineda; Patricia Ruiz; Laia Ejarque; Teresa Vendrell; Juan Antonio Camacho; Santiago Mendizábal; Artur Oliver; José Ballarín; Roser Torra; Elisabet Ars
Journal:  Pediatr Nephrol       Date:  2013-10-27       Impact factor: 3.714
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