Dominant form of congenital hyperinsulinism maps to HK1 region on 10q. - Wikidata - awgldk - TriplyDB

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

http://www.wikidata.org/entity/Q37422505

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Update on neonatal hypoglycemia.Overexpression of metabolic markers HK1 and PKM2 contributes to lymphatic metastasis and adverse prognosis in Chinese gastric cancer.Re-evaluating "transitional neonatal hypoglycemia": mechanism and implications for management Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders Congenital Hyperinsulinism in china: a review of Chinese literature over the past 15 years Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology.Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism.Congenital hyperinsulinism and Poland syndrome in association with 10p13-14 duplication.Functional and Metabolomic Consequences of KATP Channel Inactivation in Human Islets.Congenital Hyperinsulinism: Diagnosis and Treatment Update.Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities.Nutrient sensing in pancreatic islets: lessons from congenital hyperinsulinism and monogenic diabetes.

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Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

http://www.wikidata.org/entity/Q37422505

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 13 July 2013

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vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

@en

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

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type

label

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

@en

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

@nl

prefLabel

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

@en

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

@nl

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Hormone Research

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Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

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Ariella Sasson

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Arupa Ganguly

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Courtney Macmullen

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David Stokes

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Dimitrios Monos

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Hakon Hakonarson

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Jonathan Bradfield

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Kara Boodhansingh

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Karthik Ganapathy

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Katarzyna Mackiewicz

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P2860

Initial sequencing and analysis of the human genome

Human DNA2 is a mitochondrial nuclease/helicase for efficient processing of DNA replication and repair intermediates

Human Dna2 is a nuclear and mitochondrial DNA maintenance protein

The human factors YY1 and LSF repress the human immunodeficiency virus type 1 long terminal repeat via recruitment of histone deacetylase 1.

Counterregulation of chromatin deacetylation and histone deacetylase occupancy at the integrated promoter of human immunodeficiency virus type 1 (HIV-1) by the HIV-1 repressor YY1 and HIV-1 activator Tat

dbSNP: the NCBI database of genetic variation

A map of human genome variation from population-scale sequencing

The UCSC Genome Browser database: update 2011

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.

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18-27

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scholarly article

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10.1159/000351943

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1

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Charles A Stanley

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2013-07-13T00:00:00Z

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