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C T Basson

Showing results (21-30 of 37) with videos related to

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Developmental Biology|February 13, 2001
TBX5 transcription factor regulates cell proliferation during cardiogenesisC J Hatcher, M S Kim, C S Mah, et al.
The Journal of Cell Biology|March 1, 1990
Spatiotemporal segregation of endothelial cell integrin and nonintegrin extracellular matrix-binding proteins during adhesion eventsC T Basson, W J Knowles, L Bell, et al.
The New England Journal of Medicine|March 31, 1994
The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)C T Basson, G S Cowley, S D Solomon, et al.
Circulation|June 4, 1998
Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defectsD W Benson, A Sharkey, D Fatkin, et al.
The Journal of Clinical Investigation|September 1, 1995
Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3C A MacRae, N Ghaisas, S Kass, et al.
The Journal of Clinical Investigation|September 7, 2000
Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complexM Casey, C J Vaughan, J He, et al.
Genomics|August 1, 1996
Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130C T Basson, C A MacRae, M Schoenberg-Fejzo, et al.
Science (New York, N.Y.)|July 4, 1998
Congenital heart disease caused by mutations in the transcription factor NKX2-5J J Schott, D W Benson, C T Basson, et al.
Nature Genetics|August 1, 1994
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1S Kass, C MacRae, H L Graber, et al.
Circulation|May 23, 2001
Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorderC J Vaughan, M Casey, J He, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Developmental Biology|February 13, 2001
TBX5 transcription factor regulates cell proliferation during cardiogenesisC J Hatcher, M S Kim, C S Mah, et al.
The Journal of Cell Biology|March 1, 1990
Spatiotemporal segregation of endothelial cell integrin and nonintegrin extracellular matrix-binding proteins during adhesion eventsC T Basson, W J Knowles, L Bell, et al.
The New England Journal of Medicine|March 31, 1994
The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)C T Basson, G S Cowley, S D Solomon, et al.
Circulation|June 4, 1998
Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defectsD W Benson, A Sharkey, D Fatkin, et al.
The Journal of Clinical Investigation|September 1, 1995
Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3C A MacRae, N Ghaisas, S Kass, et al.
The Journal of Clinical Investigation|September 7, 2000
Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complexM Casey, C J Vaughan, J He, et al.
Genomics|August 1, 1996
Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130C T Basson, C A MacRae, M Schoenberg-Fejzo, et al.
Science (New York, N.Y.)|July 4, 1998
Congenital heart disease caused by mutations in the transcription factor NKX2-5J J Schott, D W Benson, C T Basson, et al.
Nature Genetics|August 1, 1994
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1S Kass, C MacRae, H L Graber, et al.
Circulation|May 23, 2001
Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorderC J Vaughan, M Casey, J He, et al.
Pageof 4