The genetics of pulmonary arterial hypertension in the post-BMPR2 era

por Fessel, Joshua P., Loyd, James E., Austin, Eric D.
Publicado 2011

Letter to Editor

por Weingarten, Angela J., Loyd, James E., Doyle, Thomas P.
Publicado 2016

An evidence-based knowledgebase of pulmonary arterial hypertension to identify genes and pathways relevant to pathogenesis

por Zhao, Min, Austin, Eric D., Hemnes, Anna R., Loyd, James E., Zhao, Zhongming
Publicado 2014

Adverse effects of BMPR2 suppression in macrophages in animal models of pulmonary hypertension

por West, James, Chen, Xinping, Yan, Ling, Gladson, Santhi, Loyd, James, Rizwan, Hamid, Talati, Megha
Publicado 2020

Copy-number variation in BMPR2 is not associated with the pathogenesis of pulmonary arterial hypertension

por Johnson, Jennifer A, Vnencak-Jones, Cindy L, Cogan, Joy D, Loyd, James E, West, James
Publicado 2009

Pulmonary arterial hypertension: Specialists’ knowledge, practices, and attitudes of genetic counseling and genetic testing in the USA

por Jacher, Joseph E., Martin, Lisa J., Chung, Wendy K., Loyd, James E., Nichols, William C.
Publicado 2017

Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita

por Parry, Erin M, Alder, Jonathan K, Lee, Stella S, Phillips, John A, Loyd, James E, Duggal, Priya, Armanios, Mary
Publicado 2011

A disease-associated frameshift mutation in caveolin-1 disrupts caveolae formation and function through introduction of a de novo ER retention signal

por Copeland, Courtney A., Han, Bing, Tiwari, Ajit, Austin, Eric D., Loyd, James E., West, James D., Kenworthy, Anne K.
Publicado 2017

Fibrosing mediastinitis complicating prior histoplasmosis is associated with human leukocyte antigen DQB1*04:02 − a case control study

por Strock, Stephen B, Gaudieri, Silvana, Mallal, Simon, Yu, Chang, Mitchell, Daphne, Cogan, Joy, Mason, Wendi, Crowe, Deborah, Loyd, James E
Publicado 2015

Altered prostanoid production by fibroblasts cultured from the lungs of human subjects with idiopathic pulmonary fibrosis

por Cruz-Gervis, Roberto, Stecenko, Arlene A, Dworski, Ryszard, Lane, Kirk B, Loyd, James E, Pierson, Richard, King, Gayle, Brigham, Kenneth L
Publicado 2002

Genetics and genomics of pulmonary arterial hypertension

por Morrell, Nicholas W., Aldred, Micheala A., Chung, Wendy K., Elliott, C. Gregory, Nichols, William C., Soubrier, Florent, Trembath, Richard C., Loyd, James E.
Publicado 2019

Sex hormone exposure and reproductive factors in pulmonary arterial hypertension: a case–control study

por Badlam, Jessica B., Badesch, David, Brittain, Evan, Cordell, Shannon, Ding, Tan, Fox, Kelly, Hemnes, Anna, Loyd, James, Pugh, Meredith, Robbins, Ivan, Yu, Chang, Austin, Eric D.
Publicado 2020

Aberrant caveolin-1–mediated Smad signaling and proliferation identified by analysis of adenine 474 deletion mutation (c.474delA) in patient fibroblasts: a new perspective on the m...

por Marsboom, Glenn, Chen, Zhenlong, Yuan, Yang, Zhang, Yanmin, Tiruppathi, Chinnaswamy, Loyd, James E., Austin, Eric D., Machado, Roberto F., Minshall, Richard D., Rehman, Jalees, Malik, Asrar B.
Publicado 2017

Peripheral Blood Telomere Attrition in Persons at Risk for Familial Pulmonary Fibrosis

por Salisbury, Margaret L., Markin, Cheryl R., Wu, Pingsheng, Cogan, Joy D., Mitchell, Daphne B., Liu, Qi, Loyd, James E., Lancaster, Lisa H., Kropski, Jonathan A., Blackwell, Timothy S.
Publicado 2022

Physiologic and molecular consequences of endothelial Bmpr2 mutation

por Majka, Susan, Hagen, Moira, Blackwell, Thomas, Harral, Julie, Johnson, Jennifer A, Gendron, Robert, Paradis, Helene, Crona, Daniel, Loyd, James E, Nozik-Grayck, Eva, Stenmark, Kurt R, West, James
Publicado 2011

Mast cell number, phenotype, and function in human pulmonary arterial hypertension

por Farha, Samar, Sharp, Jacqueline, Asosingh, Kewal, Park, Margaret, Comhair, Suzy A. A., Tang, W. H. Wilson, Thomas, Jim, Farver, Carol, Hsieh, Fred, Loyd, James E., Erzurum, Serpil C.
Publicado 2012

Ancestral Mutation in Telomerase Causes Defects in Repeat Addition Processivity and Manifests As Familial Pulmonary Fibrosis

por Alder, Jonathan K., Cogan, Joy D., Brown, Andrew F., Anderson, Collin J., Lawson, William E., Lansdorp, Peter M., Phillips, John A., Loyd, James E., Chen, Julian J.-L., Armanios, Mary
Publicado 2011

BMPR2 expression is suppressed by signaling through the estrogen receptor

por Austin, Eric D, Hamid, Rizwan, Hemnes, Anna R, Loyd, James E, Blackwell, Tom, Yu, Chang, Phillips III, John A, Gaddipati, Radhika, Gladson, Santhi, Gu, Everett, West, James, Lane, Kirk B
Publicado 2012

Expression of a Human Caveolin-1 Mutation in Mice Drives Inflammatory and Metabolic Defect-Associated Pulmonary Arterial Hypertension

por Rathinasabapathy, Anandharajan, Copeland, Courtney, Crabtree, Amber, Carrier, Erica J., Moore, Christy, Shay, Sheila, Gladson, Santhi, Austin, Eric D., Kenworthy, Anne K., Loyd, James E., Hemnes, Anna R., West, James D.
Publicado 2020

Truncating and missense BMPR2 mutations differentially affect the severity of heritable pulmonary arterial hypertension

por Austin, Eric D, Phillips, John A, Cogan, Joy D, Hamid, Rizwan, Yu, Chang, Stanton, Krista C, Phillips, Charles A, Wheeler, Lisa A, Robbins, Ivan M, Newman, John H, Loyd, James E
Publicado 2009