Maturity-onset diabetes of the young: from clinical description to molecular genetic characterization.
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Insights into the genetic basis of type 2 diabetesHnf6 and Tcf2 (MODY5) are linked in a gene network operating in a precursor cell domain of the embryonic pancreasSpecies-specific differences in the expression of the HNF1A, HNF1B and HNF4A genes.Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population.Evaluation of serum 1,5 anhydroglucitol levels as a clinical test to differentiate subtypes of diabetesDetailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes risk.Mild fasting hyperglycemia in children: high rate of glucokinase mutations and some risk of developing type 1 diabetes mellitus.Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pathology of insulin resistance and beta cell failure.MED25 is a mediator component of HNF4α-driven transcription leading to insulin secretion in pancreatic beta-cells.First UK survey of paediatric type 2 diabetes and MODYTCF7L2: the biggest story in diabetes genetics since HLA?Early onset of liver steatosis in a Japanese girl with maturity-onset diabetes of the young type 3 (MODY3).Expression profile of HMBOX1, a novel transcription factor, in human cancers using highly specific monoclonal antibodies.Animal models of GWAS-identified type 2 diabetes genes.Genetics of type 2 diabetes mellitus and obesity--a review.Role of HNF-1alpha in regulating the expression of genes involved in cellular growth and proliferation in pancreatic beta-cells.Type 2 diabetes and obesity: genomics and the clinic.Messenger RNA processing and its role in diabetes.The genetics of type 2 diabetes and its clinical relevance.HNF1B-associated clinical phenotypes: the kidney and beyond.Fetal anomalies associated with HNF1B mutations: report of 20 autopsy cases.Diabetes susceptibility in the Canadian Oji-Cree population is moderated by abnormal mRNA processing of HNF1A G319S transcripts.GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.A Novel Mutation of the Glucokinase Gene in Maturity-onset Diabetes of the Young Type 2 (MODY2).Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics.Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients.Heterozygous glucokinase mutations and birth weight in Spanish children.Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.Glucokinase mutations in pediatric patients with impaired fasting glucose.Genetic Testing of Maturity-Onset Diabetes of the Young Current Status and Future Perspectives.
P2860
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P2860
Maturity-onset diabetes of the young: from clinical description to molecular genetic characterization.
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Maturity-onset diabetes of the ...... ular genetic characterization.
@ast
Maturity-onset diabetes of the ...... ular genetic characterization.
@en
Maturity-onset diabetes of the ...... ular genetic characterization.
@nl
type
label
Maturity-onset diabetes of the ...... ular genetic characterization.
@ast
Maturity-onset diabetes of the ...... ular genetic characterization.
@en
Maturity-onset diabetes of the ...... ular genetic characterization.
@nl
prefLabel
Maturity-onset diabetes of the ...... ular genetic characterization.
@ast
Maturity-onset diabetes of the ...... ular genetic characterization.
@en
Maturity-onset diabetes of the ...... ular genetic characterization.
@nl
P356
P1476
Maturity-onset diabetes of the ...... ular genetic characterization.
@en
P2093
P304
P356
10.1053/BEEM.2001.0148
P577
2001-09-01T00:00:00Z