ALK5- and TGFBR2-independent role of ALK1 in the pathogenesis of hereditary hemorrhagic telangiectasia type 2

Blood

Volumn 111, Issue 2, 2008, Pages 633-642

  Park, Sung O ^a   Young, Jae Lee ^a   Seki, Tsugio ^a   Hong, Kwon Ho ^a   Fliess, Naime ^a   Jiang, Zhigang ^a   Park, Alice ^b   Wu, Xiaofang ^b   Kaartinen, Vesa ^c   Roman, Beth L ^b,d   Oh, S Paul ^a,e  

^a UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^b GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

^c UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^d UNIVERSITY OF PITTSBURGH   (United States)

^e UNIVERSITY OF FLORIDA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSFORMING GROWTH FACTOR BETA; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 1; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 2;

ALK1 GENE; ALK5 GENE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; GENE; GENE DELETION; MORPHOGENESIS; MOUSE; NONHUMAN; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE; SIGNAL TRANSDUCTION; TGFBR2 GENE; TRANSGENIC MOUSE; VASCULAR ENDOTHELIUM; ZEBRA FISH;

EID: 38349173601     PISSN: 00064971     EISSN: 00064971     Source Type: Journal    
DOI: 10.1182/blood-2007-08-107359     Document Type: Article

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