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Advances in Experimental Medicine and Biology|March 26, 2014
Application of next-generation sequencing to identify genes and mutations causing autosomal dominant retinitis pigmentosa (adRP)Stephen P Daiger, Sara J Bowne, Lori S Sullivan, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|June 26, 2007
Plexiform-like lesions and increased tissue factor expression in a rat model of severe pulmonary arterial hypertensionR James White, David F Meoli, Robert F Swarthout, et al.
Nature|March 31, 2016
Mitochondrial ROS regulate thermogenic energy expenditure and sulfenylation of UCP1Edward T Chouchani, Lawrence Kazak, Mark P Jedrychowski, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|December 20, 2018
Early repair of ventral incisional hernia may improve quality of life after surgery for abdominal malignancy: a prospective observational cohort studyM P Feng, R B Baucom, K K Broman, et al.
Plos One|December 8, 2021
The neutrophil protein CD177 is a novel PDPN receptor that regulates human cancer-associated fibroblast physiologyJillian L Astarita, Shilpa Keerthivasan, Bushra Husain, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|August 27, 2024
Research prioritization in hernia surgery: a modified Delphi ACHQC and VHOC expert consensusDaphne Remulla, Mazen R Al-Mansour, Christopher Schneider, et al.
The European Respiratory Journal|April 10, 2009
Elastin expression in very severe human COPDG Deslee, J C Woods, C M Moore, et al.
The American Journal of Pathology|May 22, 2016
Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human DiseaseScott H Greenwald, Jeremy R Charette, Magdalena Staniszewska, et al.
Molecular Vision|May 2, 2003
Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) geneSara J Bowne, Stephen P Daiger, Kimberly A Malone, et al.
Ophthalmology|March 12, 2013
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2Francesco Testa, Albert M Maguire, Settimio Rossi, et al.
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