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American Journal of Respiratory Cell and Molecular Biology|March 20, 2012
Human primary lung endothelial cells in cultureSuzy A A Comhair, Weiling Xu, Lori Mavrakis, et al.
Plos One|May 26, 2016
Mitochondrial Haplogroups and Risk of Pulmonary Arterial HypertensionSamar Farha, Bo Hu, Suzy Comhair, et al.
Human Genetics|September 1, 2004
Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testingMicheala A Aldred, Laura Baumber, Alison Hill, et al.
The American Journal of Pathology|July 28, 2004
Molecular classification of parathyroid neoplasia by gene expression profilingCarl Morrison, William Farrar, Jeff Kneile, 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.
Pulmonary Circulation|April 25, 2012
Pulmonary artery endothelium resident endothelial colony-forming cells in pulmonary arterial hypertensionHeng T Duong, Suzy A Comhair, Micheala A Aldred, et al.
Pulmonary Circulation|June 10, 2017
Genomic stability of pulmonary artery endothelial colony-forming cells in cultureKylie M Drake, Chiara Federici, Heng T Duong, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 2007
Human G(salpha) mutant causes pseudohypoparathyroidism type Ia/neonatal diarrhea, a potential cell-specific role of the palmitoylation cycleNoriko Makita, Junichiro Sato, Philippe Rondard, et al.
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