TM Frayling, CM Lindgren, JC Chevre, S Menzel, M … - Diabetes, 2003 - Am Diabetes Assoc Maturity-onset diabetes of the young (MODY) is a heterogeneous single gene disorder characterized
by non–insulin-dependent diabetes, an early onset and autosomal dominant inheritance. Mutations
in six genes have been shown to cause MODY. Approximately 15–20% of families fitting ... Cited by 41 - Related articles - BL Direct - All 6 versions
- ►shouxi.net J Wang, G Cortina, SV Wu, R Tran, JH Cho, MJ Tsai … - The New England journal …, 2006 - nejm.org Results The patients had few intestinal enteroendocrine cells positive for chromogranin A, but
they had normal numbers of Paneth's, goblet, and absorptive cells. We identified two homozygous
mutations in NEUROG3, both of which rendered the NEUROG3 protein unable to activate ... Cited by 37 - Related articles - BL Direct - All 8 versions
M Hara, X Wang, VP Paz, N Iwasaki, M Honda, Y … - Journal of Human …, 2001 - Springer M. Hara ( ) · X. Wang · VP Paz · GI Bell Howard Hughes Medical Institute, The University of
Chicago, 5841 South Maryland Avenue, MC1028, Chicago, IL 60637, USA Tel. 1-773-702-9118
; Fax 1-773-702-9237 e-mail: mhara@midway.uchicago.edu N. Iwasaki · Y. Iwamoto ... Cited by 8 - Related articles - BL Direct - All 5 versions
- ►nih.gov NL Brown, SL Dagenais, CM Chen, T Glaser - Mammalian Genome, 2002 - Springer Abstract. The human ATOH7 gene encodes a basic helix-loop- helix (bHLH) transcription factor
that is highly similar to Dro- sophila Atonal within the conserved bHLH domain. The ATOH7 coding
region is contained within a single exon. We mapped ATOH7 to Chromosome (Chr) ... Cited by 7 - Related articles - BL Direct - All 6 versions
WE Winter - Reviews in Endocrine & Metabolic Disorders, 2003 - Springer Page 1. Reviews in Endocrine & Metabolic Disorders 2003;4:43–51 C 2003 Kluwer
Academic Publishers. Manufactured in The Netherlands. Newly Defined Genetic
Diabetes Syndromes: Maturity Onset Diabetes of the Young ... Cited by 7 - Related articles - BL Direct - All 3 versions
JF Louet, SB Smith, JF Gautier, M … - Diabetes, Obesity …, 2008 - interscience.wiley.com Ketosis-prone diabetes (KPD) is a phenotypically defined form of diabetes characterized by male
predominance and severe insulin deficiency. Neurogenin3 (NGN3) is a proendocrine gene,
which is essential for the fate of pancreatic β cells. Mice lacking ngn3 develop early ... Cited by 1 - Related articles - All 2 versions
V Nocerino, C Colombo, R Bonfanti, D Iafusco … - Diabetic medicine: a …, 2009 - ncbi.nlm.nih.gov 1: Diabet Med. 2009 Jun;26(6):660-1. Mutations in IAPP and NEUROG3 genes are
not a common cause of permanent neonatal/infancy/childhood-onset diabetes. Nocerino
V, Colombo C, Bonfanti R, Iafusco D, Barbetti F. Publication ... Related articles - All 2 versions
F Barbetti, V Nocerino, C Colombo, R Bonfanti, D … - interscience.wiley.com It is also possible that your web browser is not configured or not able to display style sheets.
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