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Brain Research Bulletin
|
January 1, 1997
Deficient cation channel regulation in neurons from mice with targeted disruption of the extracellular Ca2+-sensing receptor gene
C Ye, C L Ho-Pao, M Kanazirska, et al.
Scientific Reports
|
February 27, 2016
Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies
Maryam Fish, Gasnat Shaboodien, Sarah Kraus, et al.
Nature Genetics
|
February 1, 1994
A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3
C L Shovlin, J M Hughes, E G Tuddenham, et al.
Developmental Biology
|
January 8, 2000
Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand
B G Bruneau, Z Z Bao, M Tanaka, et al.
Pediatric Nephrology (Berlin, Germany)
|
December 22, 1999
Circulating inflammatory cytokine levels in hemolytic uremic syndrome
C Litalien, F Proulx, M M Mariscalco, et al.
Circulation
|
August 20, 2003
Consequences of pressure overload on sarcomere protein mutation-induced hypertrophic cardiomyopathy
Joachim P Schmitt, Christopher Semsarian, Michael Arad, et al.
Journal of the American College of Cardiology
|
September 6, 2003
Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome
Vickas V Patel, Michael Arad, Ivan P G Moskowitz, et al.
Development (Cambridge, England)
|
May 9, 2003
Tbx5 is required for forelimb bud formation and continued outgrowth
Charalampos Rallis, Benoit G Bruneau, Jo Del Buono, et al.
The New England Journal of Medicine
|
April 12, 2008
Shared genetic causes of cardiac hypertrophy in children and adults
Hiroyuki Morita, Heidi L Rehm, Andres Menesses, et al.
Cell Reports
|
May 24, 2018
Dynamic Cellular Integration Drives Functional Assembly of the Heart's Pacemaker Complex
Michael Bressan, Trevor Henley, Jonathan D Louie, et al.
Page
of 54
Search research articles
Search
Showing results (211-220 of 533) with videos related to
Sort By:
Page
of 54
Brain Research Bulletin
|
January 1, 1997
Deficient cation channel regulation in neurons from mice with targeted disruption of the extracellular Ca2+-sensing receptor gene
C Ye, C L Ho-Pao, M Kanazirska, et al.
Scientific Reports
|
February 27, 2016
Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies
Maryam Fish, Gasnat Shaboodien, Sarah Kraus, et al.
Nature Genetics
|
February 1, 1994
A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3
C L Shovlin, J M Hughes, E G Tuddenham, et al.
Developmental Biology
|
January 8, 2000
Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand
B G Bruneau, Z Z Bao, M Tanaka, et al.
Pediatric Nephrology (Berlin, Germany)
|
December 22, 1999
Circulating inflammatory cytokine levels in hemolytic uremic syndrome
C Litalien, F Proulx, M M Mariscalco, et al.
Circulation
|
August 20, 2003
Consequences of pressure overload on sarcomere protein mutation-induced hypertrophic cardiomyopathy
Joachim P Schmitt, Christopher Semsarian, Michael Arad, et al.
Journal of the American College of Cardiology
|
September 6, 2003
Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome
Vickas V Patel, Michael Arad, Ivan P G Moskowitz, et al.
Development (Cambridge, England)
|
May 9, 2003
Tbx5 is required for forelimb bud formation and continued outgrowth
Charalampos Rallis, Benoit G Bruneau, Jo Del Buono, et al.
The New England Journal of Medicine
|
April 12, 2008
Shared genetic causes of cardiac hypertrophy in children and adults
Hiroyuki Morita, Heidi L Rehm, Andres Menesses, et al.
Cell Reports
|
May 24, 2018
Dynamic Cellular Integration Drives Functional Assembly of the Heart's Pacemaker Complex
Michael Bressan, Trevor Henley, Jonathan D Louie, et al.
Page
of 54