Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Mary K Porteous"'
Autor:
Joshua M Diamond, Mary K Porteous, Edward Cantu, Nuala J Meyer, Rupal J Shah, David J Lederer, Steven M Kawut, James Lee, Scarlett L Bellamy, Scott M Palmer, Vibha N Lama, Sangeeta M Bhorade, Maria Crespo, Ejigayehu Demissie, Keith Wille, Jonathan Orens, Pali D Shah, Ann Weinacker, David Weill, Selim Arcasoy, David S Wilkes, Lorraine B Ware, Jason D Christie, Lung Transplant Outcomes Group
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e51932 (2012)
INTRODUCTION:Primary graft dysfunction (PGD) is a significant contributor to early morbidity and mortality after lung transplantation. Increased vascular permeability in the allograft has been identified as a possible mechanism leading to PGD. Angiop
Externí odkaz:
https://doaj.org/article/25861605064c473f9a7ffb6dd6428564
Autor:
Hrishikesh S. Kulkarni, Kristy Ramphal, Lina Ma, Melanie Brown, Michelle Oyster, Kaitlyn N. Speckhart, Tsuyoshi Takahashi, Derek E. Byers, Mary K. Porteous, Laurel Kalman, Ramsey R. Hachem, Melanie Rushefski, Ja’Nia McPhatter, Marlene Cano, Daniel Kreisel, Masina Scavuzzo, Brigitte Mittler, Edward Cantu III, Katrine Pilely, Peter Garred, Jason D. Christie, John P. Atkinson, Andrew E. Gelman, Joshua M. Diamond
Publikováno v:
JCI Insight, Vol 5, Iss 17 (2020)
BACKGROUND The complement system plays a key role in host defense but is activated by ischemia/reperfusion injury (IRI). Primary graft dysfunction (PGD) is a form of acute lung injury occurring predominantly due to IRI, which worsens survival after l
Externí odkaz:
https://doaj.org/article/fcd4675013b44c0791e61c37230368a0
Autor:
Anna L. Peljto, Rachel Z. Blumhagen, Avram D. Walts, Jonathan Cardwell, Julia Powers, Tamera J. Corte, Joanne L. Dickinson, Ian Glaspole, Yuben P. Moodley, Martina Koziar Vasakova, Elisabeth Bendstrup, Jesper R. Davidsen, Raphael Borie, Bruno Crestani, Philippe Dieude, Francesco Bonella, Ulrich Costabel, Gunnar Gudmundsson, Seamas C. Donnelly, Jim Egan, Michael T. Henry, Michael P. Keane, Marcus P. Kennedy, Cormac McCarthy, Aoife N. McElroy, Joshua A. Olaniyi, Katherine M. A. O’Reilly, Luca Richeldi, Paolo M. Leone, Venerino Poletti, Francesco Puppo, Sara Tomassetti, Valentina Luzzi, Nurdan Kokturk, Nesrin Mogulkoc, Christine A. Fiddler, Nikhil Hirani, R. Gisli Jenkins, Toby M. Maher, Philip L. Molyneaux, Helen Parfrey, Rebecca Braybrooke, Timothy S. Blackwell, Peter D. Jackson, Steven D. Nathan, Mary K. Porteous, Kevin K. Brown, Jason D. Christie, Harold R. Collard, Oliver Eickelberg, Elena E. Foster, Kevin F. Gibson, Marilyn Glassberg, Daniel J. Kass, Jonathan A. Kropski, David Lederer, Angela L. Linderholm, Jim Loyd, Susan K. Mathai, Sydney B. Montesi, Imre Noth, Justin M. Oldham, Amy J. Palmisciano, Cristina A. Reichner, Mauricio Rojas, Jesse Roman, Neil Schluger, Barry S. Shea, Jeffrey J. Swigris, Paul J. Wolters, Yingze Zhang, Cecilia M. A. Prele, Juan I. Enghelmayer, Maria Otaola, Christopher J. Ryerson, Mauricio Salinas, Martina Sterclova, Tewodros H. Gebremariam, Marjukka Myllärniemi, Roberto G. Carbone, Haruhiko Furusawa, Masaki Hirose, Yoshikazu Inoue, Yasunari Miyazaki, Ken Ohta, Shin Ohta, Tsukasa Okamoto, Dong Soon Kim, Annie Pardo, Moises Selman, Alvaro U. Aranda, Moo Suk Park, Jong Sun Park, Jin Woo Song, Maria Molina-Molina, Lurdes Planas-Cerezales, Gunilla Westergren-Thorsson, Albert V. Smith, Ani W. Manichaikul, John S. Kim, Stephen S. Rich, Elizabeth C. Oelsner, R. Graham Barr, Jerome I. Rotter, Josee Dupuis, George O’Connor, Ramachandran S. Vasan, Michael H. Cho, Edwin K. Silverman, Marvin I. Schwarz, Mark P. Steele, Joyce S. Lee, Ivana V. Yang, Tasha E. Fingerlin, David A. Schwartz
Rationale: Idiopathic pulmonary fibrosis is a rare, irreversible, and progressive disease of the lungs. Common genetic variants, in addition to non-genetic factors, have been consistently associated with IPF. Rare variants identified by candidate gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0670c24aedc8efa23979477ed15d39b
http://hdl.handle.net/10044/1/101620
http://hdl.handle.net/10044/1/101620
Autor:
Nikhil Jiwrajka, Giorgos Loizidis, Karen C. Patterson, Maryl E. Kreider, Cheilonda R. Johnson, Wallace T. Miller, Eduardo Jose Mortani Barbosa, Namrata Patel, Michael F. Beers, Leslie A. Litzky, Michael D. George, Mary K. Porteous
Publikováno v:
Journal of clinical rheumatology : practical reports on rheumaticmusculoskeletal diseases. 28(5)
Background/Objective \ud Patients classified as interstitial pneumonia with autoimmune features (IPAF) have interstitial lung disease (ILD) and features of autoimmunity but do not fulfill criteria for connective tissue diseases (CTDs). Our goal was t
Autor:
Mary K. Porteous, David J. Lederer, Laurel Kalman, Elana J. Bernstein, Michelle Oyster, Jason D. Christie, Pali D. Shah, Jonathan P. Singer, Chadi A. Hage, Joshua M. Diamond, Jonathan B. Orens, Laurie D. Snyder, Edward Cantu, Keith M. Wille, Jake G. Natalini, Steven M. Kawut, Vibha N. Lama, John F. McDyer, Ann Weinacker, Lorraine B. Ware
Publikováno v:
J Heart Lung Transplant
Background Previous studies have reported similarities in long-term outcomes following lung transplantation for connective tissue disease-associated interstitial lung disease (CTD-ILD) and idiopathic pulmonary fibrosis (IPF). However, it is unknown w
Autor:
Michelle Oyster, Joshua M. Diamond, Jayaram K. Udupa, Selim M. Arcasoy, Scott M. Palmer, Hao-Min Pan, Michaela R. Anderson, David J. Lederer, Mary K. Porteous, Jason D. Christie, Steven M. Kawut, Nadine Al-Naamani, Yubing Tong, Drew A. Torigian
Publikováno v:
Ann Am Thorac Soc
Rationale: Obesity is associated with an increased risk of pulmonary hypertension (PH); however, regional adipose tissue deposition is heterogeneous with distinct cardiovascular phenotypes. Objectives: To determine the association of body mass index
Autor:
David Artis, Mary K. Porteous, Steven A. Saenz, Edward Cantu, Jason D. Christie, Joshua M. Diamond, Elia D. Tait Wojno, Laurel A. Monticelli
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 201:63-72
Rationale: Primary graft dysfunction (PGD) is the leading cause of early morbidity and mortality after lung transplantation, but the immunologic mechanisms are poorly understood. Innate lymphoid cells (ILC) are a heterogeneous family of immune cells
Autor:
Yi Luo, Denis Streltsov, Mary K. Porteous, Carly McCoubrey, Pitchumani Sivakumar, Edward Cantu, Jason D. Christie, Gabor Jarai, John Ryan Thompson, Michael F. Beers, Ron Ammar
Publikováno v:
Respiratory Research, Vol 22, Iss 1, Pp 1-13 (2021)
Respiratory Research
Respiratory Research
Background Idiopathic pulmonary fibrosis (IPF) is a fatal lung disease with a significant unmet medical need. Development of transformational therapies for IPF is challenging in part to due to lack of robust predictive biomarkers of prognosis and tre
Autor:
Anna J. Podolanczuk, Joao A. Andrade, Nishant Gupta, Ather Siddiqi, Megan L. Neely, David J. Lederer, Nina Patel, Jesse Roman, Murali Ramaswamy, Rajat Walia, Yolanda Mageto, Shirin Shafazand, Amy Hajari Case, Joseph A. Lasky, Doug Lee, Kalpalatha K. Guntupalli, Mark P. Steele, Wael Asi, Hyun J Kim, Tracy Luckhardt, Timothy Liesching, Paul Sachs, Mary E. Strek, Sally Suliman, Kevin F. Gibson, Laurie D. Snyder, David Hotchkin, Randolph J. Lipchik, Kevin R. Flaherty, Eric S. White, Justin M. Oldham, Timothy P.M. Whelan, Mary K. Porteous, Imre Noth, Craig S Conoscenti, Prema Menon, Daniel F. Dilling, Jeremy Tabak, John Fitzgerald, Scott Beegle, Marilyn K. Glassberg, Lisa Lancaster, Francis Cordova, Rishi Raj, Tessy Paul, Paul Mohabir, Mridu Gulati, Ayodeji Adegunsoye, Andrew Namen, Tristan J. Huie, Robert J. Kaner, Lake Morrison, Leann Silhan, Rany Condos, David Zhang, Zeenat Safdar, John A. Belperio, Maryl Kreider, Albert Baker, Daniel A. Culver, Tonya D. Russell, Howard J. Huang, Shaun Bender, Barry Sigal, Jason Lobo
Publikováno v:
Respiratory Research
Respiratory Research, Vol 22, Iss 1, Pp 1-9 (2021)
Respiratory Research, Vol 22, Iss 1, Pp 1-9 (2021)
Background Hospitalizations are common among patients with idiopathic pulmonary fibrosis (IPF). We investigated the impact of hospitalizations on outcomes in patients with IPF. Methods The IPF-PRO Registry is an observational US registry that enrolle
Autor:
Selim M. Arcasoy, John S. Kim, Jonathan P. Singer, Michaela R. Anderson, Joshua M. Diamond, David J. Lederer, Grace Gallagher, Mary K. Porteous, Jayaram K. Udupa, Drew A. Torigian, Imaani Easthausen, Yubing Tong, R. Graham Barr, Matthew R. Baldwin, John R. Greenland, Jasleen Kukreja, Dympna Gallagher, Jason D. Christie, Scott M. Palmer, Laurie D. Snyder, Edward Cantu, Meghan Aversa, Steven R. Hays, Luke Benvenuto
Publikováno v:
Thorax
Thorax, vol 75, iss 9
Thorax, vol 75, iss 9
CT measurement of body composition may improve lung transplant candidate selection. We assessed whether skeletal muscle adipose deposition on abdominal and thigh CT scans was associated with 6 min walk distance (6MWD) and wait-list survival in lung t