Notch1 activation in mice causes arteriovenous malformations phenocopied by EphrinB2 and EphB4 mutants

Genesis

Volumn 48, Issue 3, 2010, Pages 146-150

  Krebs, Luke T ^a   Starling, Christa ^a   Chervonsky, Alexander V ^a,b   Gridley, Thomas ^a  

^a JACKSON LABORATORY   (United States)

^b UNIVERSITY OF CHICAGO   (United States)

Author keywords

Angiogenesis; Arteriovenous malformation; EphB4; EphrinB2; Notch signaling pathway; Vascular morphogenesis

Indexed keywords

EPHRIN B2; EPHRINB4; NOTCH1 RECEPTOR; UNCLASSIFIED DRUG;

ARTERIOVENOUS MALFORMATION; ARTICLE; ENDOTHELIUM CELL; GENE DELETION; GENE MUTATION; HISTOPATHOLOGY; IMMUNOHISTOCHEMISTRY; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL;

ANIMALS; ARTERIOVENOUS MALFORMATIONS; EMBRYO, MAMMALIAN; EPHRIN-B2; IMMUNOHISTOCHEMISTRY; MICE; MICE, KNOCKOUT; PHENOTYPE; RECEPTOR, EPHB4; RECEPTOR, NOTCH1; SIGNAL TRANSDUCTION;

MAMMALIA; MUS; VERTEBRATA;

EID: 77949357053     PISSN: 1526954X     EISSN: 1526968X     Source Type: Journal    
DOI: 10.1002/dvg.20599     Document Type: Article

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