Neonatal diabetes mellitus: a model for personalized medicine - Wikidata - awgldk - TriplyDB

Neonatal diabetes mellitus: a model for personalized medicine

Neonatal diabetes mellitus: a model for personalized medicine

http://www.wikidata.org/entity/Q34037120

about

Genetics and pathophysiology of neonatal diabetes mellitus.The cost-effectiveness of personalized genetic medicine: the case of genetic testing in neonatal diabetes.Sulfonylurea treatment before genetic testing in neonatal diabetes: pros and cons Disruption of a novel Kruppel-like transcription factor p300-regulated pathway for insulin biosynthesis revealed by studies of the c.-331 INS mutation found in neonatal diabetes mellitus.The Krüppel-like zinc finger protein GLIS3 transactivates neurogenin 3 for proper fetal pancreatic islet differentiation in mice.Creation of the Web-based University of Chicago Monogenic Diabetes Registry: using technology to facilitate longitudinal study of rare subtypes of diabetes Clinical and metabolic features of adult-onset diabetes caused by ABCC8 mutations.Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes Ion channels and regulation of insulin secretion in human β-cells: a computational systems analysis Diabetes mellitus due to the toxic misfolding of proinsulin variants.Current understanding of K ATP channels in neonatal diseases: focus on insulin secretion disorders.Insulin gene mutations and diabetes Monogenic diabetes: Implementation of translational genomic research towards precision medicine.Neonatal Diabetes and the KATP Channel: From Mutation to Therapy.Sulfonylurea treatment in an infant with transient neonatal diabetes mellitus caused by an adenosine triphosphate binding cassette subfamily C member 8 gene mutation.Sulfonylurea for the treatment of neonatal diabetes owing to KATP-channel mutations: a systematic review and meta-analysis.Understanding childhood diabetes mellitus: new pathophysiological aspects.Early transition from insulin to sulfonylureas in neonatal diabetes and follow-up: Experience from China.A novel NEUROG3 mutation in neonatal diabetes associated with a neuro-intestinal syndrome.Personalized precision medicine in extreme preterm infants with transient neonatal diabetes mellitus.Identification of insulin gene variants in neonatal diabetes.Early insulin therapy prevents beta cell loss in a mouse model for permanent neonatal diabetes (Munich Ins2 C95S)The diagnosis and management of monogenic diabetes in children and adolescents

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Neonatal diabetes mellitus: a model for personalized medicine

http://www.wikidata.org/entity/Q34037120

description

2010 nî lūn-bûn

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Neonatal diabetes mellitus: a model for personalized medicine

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Neonatal diabetes mellitus: a model for personalized medicine

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J.TEM.2010.03.004

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Trends in Endocrinology and Metabolism

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Neonatal diabetes mellitus: a model for personalized medicine

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Graeme I Bell

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Louis H Philipson

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Rochelle N Naylor

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Siri Atma W Greeley

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P2860

Neonatal Diabetes Mellitus and Neonatal Polycystic, Dysplastic Kidneys: Phenotypically Discordant Recurrence of a Mutation in the Hepatocyte Nuclear Factor-1β Gene Due to Germline Mosaicism

Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1? in human pancreatic development

Rfx6 directs islet formation and insulin production in mice and humans

The G53D mutation in Kir6.2 (KCNJ11) is associated with neonatal diabetes and motor dysfunction in adulthood that is improved with sulfonylurea therapy.

Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence

Mutations in PTF1A cause pancreatic and cerebellar agenesis

Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes

Impaired glucose homeostasis in transgenic mice expressing the human transient neonatal diabetes mellitus locus, TNDM

A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes

A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes.

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464-472

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scholarly article

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10.1016/J.TEM.2010.03.004

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8

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20434356

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