Abnormal cardiac inflow patterns during postnatal development in a mouse model of Holt-Oram syndrome

American Journal of Physiology - Heart and Circulatory Physiology

Volumn 289, Issue 3 58-3, 2005, Pages

  Zhou, Yu Qing ^a   Zhu, Yonghong ^a,b   Bishop, Jonathan ^a   Davidson, Lorinda ^a   Henkelman, R Mark ^a,b,c   Bruneau, Benoit G ^a,b,c   Foster, F Stuart ^a,b,c  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY OF TORONTO   (Canada)

Author keywords

Atrial septal defect; Doppler flow sampling; Left ventricular diastolic function; Right ventricular dilatation; Tbx5 mutation

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; B SCAN; BIOMICROSCOPY; BODY WEIGHT; CONTROLLED STUDY; FEMALE; GENE; GENE EXPRESSION; GENE MUTATION; HEART ATRIUM SEPTUM DEFECT; HEART LEFT VENTRICLE ENDDIASTOLIC PRESSURE; HEART LEFT VENTRICLE FILLING; HEART LEFT VENTRICLE FUNCTION; HEART LEFT VENTRICLE HYPERTROPHY; HEART RATE; HOLT ORAM SYNDROME; M MODE ECHOCARDIOGRAPHY; MALE; MOUSE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; TBX5 GENE; TWO DIMENSIONAL ECHOCARDIOGRAPHY;

ANIMALS; DIASTOLE; DISEASE MODELS, ANIMAL; ECHOCARDIOGRAPHY; FEMALE; HEART; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, ATRIAL; MALE; MICE; MICE, MUTANT STRAINS; PHENOTYPE; SYSTOLE; T-BOX DOMAIN PROTEINS; VENTRICULAR DYSFUNCTION, LEFT; VENTRICULAR DYSFUNCTION, RIGHT;

EID: 23944450566     PISSN: 03636135     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpheart.00027.2005     Document Type: Article

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