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E Seidman

Showing results (231-240 of 533) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 5, 2013
An RNA-seq protocol to identify mRNA expression changes in mouse diaphyseal bone: applications in mice with bone property altering Lrp5 mutationsUgur M Ayturk, Christina M Jacobsen, Danos C Christodoulou, 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.
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 9, 2012
Exercise training improves cardiac function and attenuates arrhythmia in CPVT miceEfrat Kurtzwald-Josefson, Edith Hochhauser, Guy Katz, et al.
The Journal of Clinical Investigation|June 24, 1998
Regulation of murine fetal-placental calcium metabolism by the calcium-sensing receptorC S Kovacs, C L Ho-Pao, J L Hunzelman, et al.
Journal of Molecular and Cellular Cardiology|January 15, 2013
Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathyBradley M Palmer, Joachim P Schmitt, Christine E Seidman, et al.
Nature Genetics|December 1, 1995
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathyH Watkins, D Conner, L Thierfelder, et al.
American Journal of Community Psychology|June 1, 1995
Development and validation of adolescent-perceived microsystem scales: social support, daily hassles, and involvementE Seidman, L Allen, J L Aber, et al.
Biochemistry|April 15, 1997
Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and functionN Golitsina, Y An, N J Greenfield, et al.
Biochemical Pharmacology|February 12, 2008
Increased glycogen stores due to gamma-AMPK overexpression protects against ischemia and reperfusion damageMichal Ofir, Michael Arad, Eyal Porat, et al.
The Journal of Clinical Investigation|January 12, 1999
Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain geneD Fatkin, M E Christe, O Aristizabal, et al.
Pageof 54

Showing results (231-240 of 533) with videos related to

Sort By:
Pageof 54
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 5, 2013
An RNA-seq protocol to identify mRNA expression changes in mouse diaphyseal bone: applications in mice with bone property altering Lrp5 mutationsUgur M Ayturk, Christina M Jacobsen, Danos C Christodoulou, 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.
Journal of Applied Physiology (Bethesda, Md. : 1985)|October 9, 2012
Exercise training improves cardiac function and attenuates arrhythmia in CPVT miceEfrat Kurtzwald-Josefson, Edith Hochhauser, Guy Katz, et al.
The Journal of Clinical Investigation|June 24, 1998
Regulation of murine fetal-placental calcium metabolism by the calcium-sensing receptorC S Kovacs, C L Ho-Pao, J L Hunzelman, et al.
Journal of Molecular and Cellular Cardiology|January 15, 2013
Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathyBradley M Palmer, Joachim P Schmitt, Christine E Seidman, et al.
Nature Genetics|December 1, 1995
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathyH Watkins, D Conner, L Thierfelder, et al.
American Journal of Community Psychology|June 1, 1995
Development and validation of adolescent-perceived microsystem scales: social support, daily hassles, and involvementE Seidman, L Allen, J L Aber, et al.
Biochemistry|April 15, 1997
Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and functionN Golitsina, Y An, N J Greenfield, et al.
Biochemical Pharmacology|February 12, 2008
Increased glycogen stores due to gamma-AMPK overexpression protects against ischemia and reperfusion damageMichal Ofir, Michael Arad, Eyal Porat, et al.
The Journal of Clinical Investigation|January 12, 1999
Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain geneD Fatkin, M E Christe, O Aristizabal, et al.
Pageof 54