Mesodermal Pten inactivation leads to alveolar capillary dysplasia-like phenotype

Journal of Clinical Investigation

Volumn 122, Issue 11, 2012, Pages 3862-3872

  Tiozzo, Caterina ^a,b,f   Carraro, Gianni ^b,c   Al Alam, Denise ^b   Baptista, Sheryl ^b   Danopoulos, Soula ^b   Li, Aimin ^a   Lavarreda Pearce, Maria ^b   Li, Changgong ^a   De Langhe, Stijn ^d   Chan, Belinda ^a   Borok, Zea ^a   Bellusci, Saverio ^b,c   Minoo, Parviz ^a,e  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b CHILDREN S HOSPITAL LOS ANGELES   (United States)

^c JUSTUS LIEBIG UNIVERSITY GIESSEN   (Germany)

^d DEPARTMENT OF MEDICINE   (United States)

^e WOMEN S AND CHILDREN S HOSPITAL   (United States)

^f NASSAU UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; PROTEIN KINASE B;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CELL DIFFERENTIATION; CELL LINEAGE; CONGENITAL ALVEOLAR CAPILLARY DYSPLASIA; CONTROLLED STUDY; EMBRYO; GENE; GENE EXPRESSION PROFILING; GENE INACTIVATION; HEMANGIOBLAST; HUMAN; HUMAN TISSUE; MOUSE; NEWBORN; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PTEN GENE; PULMONARY VASCULAR DISEASE;

ANIMALS; CELL DIFFERENTIATION; CELL LINEAGE; ENDOTHELIAL CELLS; ENZYME ACTIVATION; FORKHEAD TRANSCRIPTION FACTORS; HUMANS; LUNG; MESODERM; MICE; MICE, KNOCKOUT; PERSISTENT FETAL CIRCULATION SYNDROME; PHENOTYPE; PROTO-ONCOGENE PROTEINS C-AKT; PTEN PHOSPHOHYDROLASE; PULMONARY ALVEOLI;

EID: 84868620747     PISSN: 00219738     EISSN: 15588238     Source Type: Journal    
DOI: 10.1172/JCI61334     Document Type: Article

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