A Brackenridge, ER Pearson, F Shojaee- … - Diabetes, 2006 - Am Diabetes Assoc Heterozygous mutations in the transcription factors hepatocyte nuclear factor
(HNF)-1α and -1β result in MODY (maturity-onset diabetes of the young).
Despite structural similarity between HNF-1α and -1β, HNF-1β mutation ... Cited by 16 - Related articles - BL Direct - All 5 versions
- ►shouxi.net A Brackenridge, ER Pearson, F Shojaee- … - Diabetes, 2006 - Am Diabetes Assoc Production Rate in Subjects With Hepatocyte Nuclear ... Anna Brackenridge, 1
Ewan R. Pearson, 2 Fariba Shojaee-Moradie, 3 Andrew T. Hattersley, 2 ... David
Russell-Jones, 1 and A. Margot Umpleby 3 ... Heterozygous mutations in the ... Cited by 2 - Related articles - All 2 versions
D Beckers, C Bellanné-Chantelot, M Maes - The Journal of pediatrics, 2007 - Elsevier This patient was originally described in 1996 by Devriendt et al 6 as having
atypical Alagille syndrome. The child is now 18 years of age, and an HNF-1β
mutation has recently been established. The patient was a growth-retarded ... Cited by 8 - Related articles - All 9 versions
- Free from Publisher ER Pearson, MK Badman, CR Lockwood, PM … - Diabetes Care, 2004 - Am Diabetes Assoc OBJECTIVE—Mutations in the highly homologous transcription factors hepatocyte
nuclear factor (HNF)-1α and -1β cause maturity-onset diabetes of the young
types 3 and 5, respectively. Diabetes due to HNF-1α mutations is well ... Cited by 33 - Related articles - BL Direct - All 6 versions
K Raile, E Klopocki, T Wessel, D Deiss, D Horn … - Diabetes care, 2008 - Am Diabetes Assoc Mature-onset diabetes of the young 5 (MODY5) is characterized by a wide clinical
spectrum, including diabetes and kidney disease (1–3). Associated gene defects
are either mutations within HNF1B or a 1.4–1.5 Mb monoallelic deletion of ... Cited by 2 - Related articles - All 3 versions
[CITATION] Fetal growth is altered by fetal genotype and not insulin treatment of maternal …
K Pilgaard, CB Jensen, JH Schou, V Lyssenko, … - Diabetologia, 2009 - Springer Abstract Aims/hypothesis We studied the physiological, metabolic and hormonal
mechanisms underlying the elevated risk of type 2 diabetes in carriers of TCF7L2
gene. Methods We undertook genotyping of 81 healthy young Danish men for ... Cited by 6 - Related articles - All 2 versions
D Müller, E Klopocki, LM Neumann, S … - Kidney international, 2006 - cat.inist.fr A complex phenotype with cystic renal disease. D MÜLLER, E KLOPOCKI, LM NEUMANN,
S MUNDLOS, M TAUPITZ, I SCHULZE, HH ROPERS, U QUERFELD ... Cited by 7 - Related articles - BL Direct - All 3 versions
- ►oxfordjournals.org C Haumaitre, M Fabre, S Cormier, C Baumann … - Human molecular genetics, 2006 - Oxford Univ Press Heterozygous mutations in the HNF1ß/vHNF1/TCF2 gene cause maturity-onset
diabetes of the young (MODY5), associated with severe renal disease and abnormal
genital tract. Here, we characterize two fetuses, a 27-week male and a ... Cited by 29 - Related articles - BL Direct - All 6 versions
- ►diabetesjournals.org [PDF] M Shepherd, ER Pearson, J Houghton, G Salt, … - Diabetes Care, 2003 - Am Diabetes Assoc Type 1 diabetes is associated with other autoimmune diseases. Many diabetes
centers routinely screen patients with type 1 diabetes for auto- immune thyroid
disease (ATD). The pres- ence of two autoimmune diseases raises the ... Cited by 35 - Related articles - BL Direct - All 5 versions
