Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus. - Wikidata - awgldk - TriplyDB

Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus.

Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus.

http://www.wikidata.org/entity/Q54340488

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Maturity-Onset Diabetes of the Young: What Do Clinicians Need to Know?Undiagnosed MODY: Time for Action Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families.Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population.Molecular diagnosis of maturity onset diabetes of the young in India.Systematic Population Screening, Using Biomarkers and Genetic Testing, Identifies 2.5% of the U.K. Pediatric Diabetes Population With Monogenic Diabetes.A Single Nucleotide Variant in HNF-1β is Associated with Maturity-Onset Diabetes of the Young in a Large Chinese Family.Abnormalities in chromosome 6q24 as a cause of early-onset, non-obese, non-autoimmune diabetes mellitus without history of neonatal diabetes.Efficacy and safety of alogliptin in a pediatric patient with maturity-onset diabetes of the young type 1.GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.A Case of Novel Mutation of HNF1B in Maturity-onset Diabetes of the Young Type 5 (MODY5)South Asian individuals with diabetes who are referred for MODY testing in the UK have a lower mutation pick-up rate than white European people.Clinical heterogeneity of abnormal glucose homeostasis associated with the HNF4A R311H mutation.Maturity-onset diabetes of the young (MODY) as a model for elucidating the multifactorial origin of type 2 diabetes mellitus.Comprehensive screening for monogenic diabetes in 89 Japanese children with insulin-requiring antibody-negative type 1 diabetes.Genetic and clinical characteristics of Chinese children with Glucokinase-maturity-onset diabetes of the young (GCK-MODY).Screening of diabetes of youth for hepatocyte nuclear factor 1 mutations: clinical phenotype of HNF1β-related maturity-onset diabetes of the young and HNF1α-related maturity-onset diabetes of the young in Japanese.Molecular and clinical characterization of glucokinase maturity-onset diabetes of the young (GCK-MODY) in Japanese patients.Incidental mild hyperglycemia in children: two MODY 2 families identified in Brazilian subjects.A Novel p.L145Q Mutation in the HNF1B Gene in a Case of Maturity-onset Diabetes of the Young Type 5 (MODY5).

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Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus.

http://www.wikidata.org/entity/Q54340488

description

2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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2011年學術文章

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Comprehensive molecular analys ...... t MODY-type diabetes mellitus.

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Comprehensive molecular analys ...... t MODY-type diabetes mellitus.

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Comprehensive molecular analys ...... t MODY-type diabetes mellitus.

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Comprehensive molecular analys ...... t MODY-type diabetes mellitus.

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Comprehensive molecular analys ...... t MODY-type diabetes mellitus.

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Comprehensive molecular analys ...... t MODY-type diabetes mellitus.

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J.1399-5448.2011.00827.X

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Pediatric Diabetes

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Comprehensive molecular analys ...... t MODY-type diabetes mellitus.

@en

P2093

Hironori Nagasaka

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Katsuya Aizu

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Kazuhiko Jinno

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Koji Kobayashi

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Momoko Shiozaki

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Nobuyoshi Tamagawa

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Rika Fujimaru

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Tatsuhiko Urakami

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Tohru Yorifuji

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Toshihiro Tajima

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P2860

Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

Human hepatocyte nuclear factor 4 isoforms are encoded by distinct and differentially expressed genes

Homeostasis model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin concentrations in man

A missense mutation of Pax4 gene (R121W) is associated with type 2 diabetes in Japanese

Beta-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors.

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.

Monogenic diabetes in the young, pharmacogenetics and relevance to multifactorial forms of type 2 diabetes.

Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes.

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26-32

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scholarly article

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10.1111/J.1399-5448.2011.00827.X

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1

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13

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2011-11-08T00:00:00Z

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22060211

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