(Q28283975)

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Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome

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scholarly article

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Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome (English)

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congenital disorder

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Alagille syndrome

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Manfred Gessler

object named as

Manfred Gessler

7

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author name string

Andreas Fischer

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Barbara Klamt

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Nina Schumacher

3

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Christiane Glaeser

4

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Ingo Hansmann

5

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Hartmut Fenge

6

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language of work or name

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publication date

September 2004

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Mammalian Genome

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15

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9

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711-6

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The Notch target genes Hey1 and Hey2 are required for embryonic vascular development

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https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic assembly of the heart: implications for congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ventricular septal defect and cardiomyopathy in mice lacking the transcription factor CHF1/Hey2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mouse model of Alagille syndrome: Notch2 as a genetic modifier of Jag1 haploinsufficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental mosaicism of JAG1 mutations in families with Alagille syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gridlock signalling pathway fashions the first embryonic artery

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

gridlock, an HLH gene required for assembly of the aorta in zebrafish

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Closure of ventricular septal defects: a study of factors influencing spontaneous and surgical closure

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HERP1 is a cell type-specific primary target of Notch

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

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Tricuspid atresia. A re-evaluation and classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

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Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of Alagille's syndrome with translocation (4;14) (q21;q21)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative analysis of the human and mouse Hey1 promoter: Hey genes are new Notch target genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Jagged1 mutations in alagille syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the human and mouse HEY1, HEY2, and HEYL genes: cloning, mapping, and mutation screening of a new bHLH gene family

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of ventricular septal defect with special reference to spontaneous closure rate, subaortic ridge and aortic valve prolapse

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hey bHLH factors in cardiovascular development.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15389319

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1007/S00335-004-2389-X

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