Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Elisabeth D. Willers"'
Autor:
Timothy N. Holt, John A. Phillips, Rizwan Hamid, Shafia S. Memon, John H. Newman, Lora K. Hedges, Bethany Womack, Lisa Wheeler, Elisabeth D. Willers
Publikováno v:
Pulmonary Circulation
High-altitude pulmonary hypertension (HAPH) is a consequence of chronic alveolar hypoxia, leading to hypoxic vasoconstriction and remodeling of the pulmonary circulation. Brisket disease in cattle is a naturally occurring animal model of hypoxic pulm
Autor:
Gérald Simonneau, Jude J. McElroy, Marc Humbert, Kari E. Roberts, Elisabeth D. Willers, Krista C. Stanton, Benjamin Sztrymf, Melissa A. Prince, Lisa Wheeler, John H. Newman, James A. Knowles, James E. Loyd, John A. Phillips, Robyn J. Barst, Ivan M. Robbins, Daniel W. Byrne, James R. Runo, Joy A. Cogan, Jane A. Morse
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 173:798-802
Rationale: Serotonin is a pulmonary vasoconstrictor and smooth muscle cell mitogen. The serotonin transporter (SERT) is abundant in pulmonary vascular smooth muscle. Compared with the short (S) allele, the long (L) SERT promoter allele is associated
Autor:
Elisabeth D. Willers, John H. Newman
Publikováno v:
Chest. 130:1633-1635
Publikováno v:
C56. PULMONARY AND NON-PULMONARY CRITICAL CARE: GREAT CASES!.
Publikováno v:
B105. CASE REPORTS: DRUGS AND DEVICES IN CRITICAL CARE.
Autor:
Elisabeth D. Willers, Ivan M. Robbins
Publikováno v:
Contemporary Cardiology™ ISBN: 9781588296610
Most of what is known about the genetic basis of pulmonary hypertension (PH) is related to mutations in bone morphogenetic protein receptor 2 (BMPR2), which have been identified in patients with pulmonary arterial hypertension (PAH). However, a numbe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82f513b64d99628870c07d849f6e76f3
https://doi.org/10.1007/978-1-60327-075-5_5
https://doi.org/10.1007/978-1-60327-075-5_5
Autor:
Elisabeth D, Willers, John H, Newman
Publikováno v:
Chest. 130(6)