Neonatal diabetes and congenital malabsorptive diarrhea attributable to a novel mutation in the human neurogenin-3 gene coding sequence - Wikidata - wikimedia - TriplyDB

Neonatal diabetes and congenital malabsorptive diarrhea attributable to a novel mutation in the human neurogenin-3 gene coding sequence

Neonatal diabetes and congenital malabsorptive diarrhea attributable to a novel mutation in the human neurogenin-3 gene coding sequence

http://www.wikidata.org/entity/Q35101836

about

Genome-edited human stem cell-derived beta cells: a powerful tool for drilling down on type 2 diabetes GWAS biology Infantile onset diabetes mellitus in developing countries - India Pancreas development in humans Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment Generating human intestinal tissues from pluripotent stem cells to study development and disease Many faces of monogenic diabetes Impaired enteroendocrine development in intestinal-specific Islet1 mouse mutants causes impaired glucose homeostasis.The Basic Helix-Loop-Helix Transcription Factor NEUROG3 Is Required for Development of the Human Endocrine Pancreas.Dissecting Human Gene Functions Regulating Islet Development With Targeted Gene Transduction Congenital diarrheal disorders: an updated diagnostic approach.Neurogenin3 cooperates with Foxa2 to autoactivate its own expression.Conditional deletion of neurogenin-3 using Nkx2.1iCre results in a mouse model for the central control of feeding, activity and obesity Mouse muscle as an ectopic permissive site for human pancreatic development.Neonatal diabetes, gallbladder agenesis, duodenal atresia, and intestinal malrotation caused by a novel homozygous mutation in RFX6.Genome Editing of Lineage Determinants in Human Pluripotent Stem Cells Reveals Mechanisms of Pancreatic Development and Diabetes.Genome editing in human pluripotent stem cells: a systematic approach unrevealing pancreas development and disease.Neurogenin 3 is important but not essential for pancreatic islet development in humans.A novel NEUROG3 mutation in neonatal diabetes associated with a neuro-intestinal syndrome.Differentiation of Islet Progenitors Regulated by Nicotinamide into Transcriptome-Verified β Cells That Ameliorate Diabetes.Mutant neurogenin-3 in a Turkish boy with congenital malabsorptive diarrhea.Extremely rare cause of congenital diarrhea: enteric anendocrinosis.Endocrine lineage biases arise in temporally distinct endocrine progenitors during pancreatic morphogenesis

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P2860

Neonatal diabetes and congenital malabsorptive diarrhea attributable to a novel mutation in the human neurogenin-3 gene coding sequence

http://www.wikidata.org/entity/Q35101836

description

2011 nî lūn-bûn

@nan

2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

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2011年论文

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name

Neonatal diabetes and congenit ...... rogenin-3 gene coding sequence

@ast

Neonatal diabetes and congenit ...... rogenin-3 gene coding sequence

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type

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Neonatal diabetes and congenit ...... rogenin-3 gene coding sequence

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Neonatal diabetes and congenit ...... rogenin-3 gene coding sequence

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prefLabel

Neonatal diabetes and congenit ...... rogenin-3 gene coding sequence

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Neonatal diabetes and congenit ...... rogenin-3 gene coding sequence

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P1433

The Journal of Clinical Endocrinology and Metabolism

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Neonatal diabetes and congenit ...... rogenin-3 gene coding sequence

@en

P2093

Diva D De León

http://www.w3.org/2001/XMLSchema#string

Doris A Stoffers

http://www.w3.org/2001/XMLSchema#string

Jennifer Oliver-Krasinski

http://www.w3.org/2001/XMLSchema#string

Linda Ernst

http://www.w3.org/2001/XMLSchema#string

Nkecha Hughes

http://www.w3.org/2001/XMLSchema#string

Pierre Russo

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Puja Patel

http://www.w3.org/2001/XMLSchema#string

Sara E Pinney

http://www.w3.org/2001/XMLSchema#string

P2860

Neurogenin3 activates the islet differentiation program while repressing its own expression

Rfx6 directs islet formation and insulin production in mice and humans

Polymorphic variations in the neurogenic differentiation-1, neurogenin-3, and hepatocyte nuclear factor-1alpha genes contribute to glucose intolerance in a South Indian population

IA1 is NGN3-dependent and essential for differentiation of the endocrine pancreas.

Diabetes, defective pancreatic morphogenesis, and abnormal enteroendocrine differentiation in BETA2/neuroD-deficient mice

neurogenin3 is required for the development of the four endocrine cell lineages of the pancreas

Control of endodermal endocrine development by Hes-1

Neurogenin 3 is essential for the proper specification of gastric enteroendocrine cells and the maintenance of gastric epithelial cell identity

Independent development of pancreatic alpha- and beta-cells from neurogenin3-expressing precursors: a role for the notch pathway in repression of premature differentiation

Direct evidence for the pancreatic lineage: NGN3+ cells are islet progenitors and are distinct from duct progenitors

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1960-1965

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scholarly article

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10.1210/JC.2011-0029

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7

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96

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2011-04-13T00:00:00Z

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21490072

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Afọ ọsịsa

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3135203

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