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Richard C Trembath

Showing results (21-30 of 169) with videos related to

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Human Molecular Genetics|August 31, 2004
A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groupsFrancesca Capon, Michael H Allen, Mahreen Ameen, et al.
Human Molecular Genetics|March 6, 2012
BMPR-II deficiency elicits pro-proliferative and anti-apoptotic responses through the activation of TGFβ-TAK1-MAPK pathways in PAHMd Talat Nasim, Takeshi Ogo, Hasnin M Chowdhury, et al.
Human Molecular Genetics|October 30, 2003
Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertensionRajiv D Machado, Nung Rudarakanchana, Carl Atkinson, et al.
Circulation|April 10, 2002
Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptorCarl Atkinson, Susan Stewart, Paul D Upton, et al.
American Journal of Medical Genetics|October 31, 2002
Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophyMicheala A Aldred, Salim Aftimos, Christine Hall, et al.
Human Molecular Genetics|July 24, 2008
Failure of bone morphogenetic protein receptor trafficking in pulmonary arterial hypertension: potential for rescueAnastasia Sobolewski, Nung Rudarakanchana, Paul D Upton, et al.
American Journal of Respiratory and Critical Care Medicine|July 17, 2013
Assessment of a pulmonary origin for blood outgrowth endothelial cells by examination of identical twins harboring a BMPR2 mutationMark L Ormiston, Laura Southgate, Carmen Treacy, et al.
The European Respiratory Journal|August 29, 2024
Genetics and precision genomics approaches to pulmonary hypertensionEric D Austin, Micheala A Aldred, Mona Alotaibi, et al.
American Journal of Human Genetics|February 16, 2005
Genetic association analysis using data from triads and unrelated subjectsMichael P Epstein, Colin D Veal, Richard C Trembath, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defectsKatie M G Snape, Deborah Ruddy, Martin Zenker, et al.
Pageof 17

Showing results (21-30 of 169) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|August 31, 2004
A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groupsFrancesca Capon, Michael H Allen, Mahreen Ameen, et al.
Human Molecular Genetics|March 6, 2012
BMPR-II deficiency elicits pro-proliferative and anti-apoptotic responses through the activation of TGFβ-TAK1-MAPK pathways in PAHMd Talat Nasim, Takeshi Ogo, Hasnin M Chowdhury, et al.
Human Molecular Genetics|October 30, 2003
Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertensionRajiv D Machado, Nung Rudarakanchana, Carl Atkinson, et al.
Circulation|April 10, 2002
Primary pulmonary hypertension is associated with reduced pulmonary vascular expression of type II bone morphogenetic protein receptorCarl Atkinson, Susan Stewart, Paul D Upton, et al.
American Journal of Medical Genetics|October 31, 2002
Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophyMicheala A Aldred, Salim Aftimos, Christine Hall, et al.
Human Molecular Genetics|July 24, 2008
Failure of bone morphogenetic protein receptor trafficking in pulmonary arterial hypertension: potential for rescueAnastasia Sobolewski, Nung Rudarakanchana, Paul D Upton, et al.
American Journal of Respiratory and Critical Care Medicine|July 17, 2013
Assessment of a pulmonary origin for blood outgrowth endothelial cells by examination of identical twins harboring a BMPR2 mutationMark L Ormiston, Laura Southgate, Carmen Treacy, et al.
The European Respiratory Journal|August 29, 2024
Genetics and precision genomics approaches to pulmonary hypertensionEric D Austin, Micheala A Aldred, Mona Alotaibi, et al.
American Journal of Human Genetics|February 16, 2005
Genetic association analysis using data from triads and unrelated subjectsMichael P Epstein, Colin D Veal, Richard C Trembath, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defectsKatie M G Snape, Deborah Ruddy, Martin Zenker, et al.
Pageof 17