The Human ABCG1 Transporter Mobilizes Plasma Membrane and Late Endosomal Non-Sphingomyelin-Associated-Cholesterol for Efflux and Esterification

Por Neufeld, Edward B., O’Brien, Katherine, Walts, Avram D., Stonik, John A., Malide, Daniela, Combs, Christian A., Remaley, Alan T.
Publicado no Biology (Basel) (2014)

Cryopyrin-associated Periodic Syndrome Caused by a Myeloid-Restricted Somatic NLRP3 Mutation

Por Zhou, Qing, Aksentijevich, Ivona, Wood, Geryl M., Walts, Avram D., Hoffmann, Patrycja, Remmers, Elaine F., Kastner, Daniel L., Ombrello, Amanda K.
Publicado no Arthritis Rheumatol (2015)

Cellular Localization and Trafficking of the Human ABCG1 Transporter

Por Neufeld, Edward B., O’Brien, Katherine, Walts, Avram D., Stonik, John A., Demosky, Steven J., Malide, Daniela, Combs, Christian A., Remaley, Alan T.
Publicado no Biology (Basel) (2014)

Preclinical Pulmonary Fibrosis Circulating Protein Biomarkers

Por Mathai, Susan K., Cardwell, Jonathan, Metzger, Fabian, Powers, Julia, Walts, Avram D., Kropski, Jonathan A., Eickelberg, Oliver, Hauck, Stefanie M., Yang, Ivana V., Schwartz, David A.
Publicado no Am J Respir Crit Care Med (2020)

MUC5B Promoter Variant rs35705950 Affects MUC5B Expression in the Distal Airways in Idiopathic Pulmonary Fibrosis

Por Nakano, Yasushi, Yang, Ivana V., Walts, Avram D., Watson, Alan M., Helling, Britney A., Fletcher, Ashley A., Lara, Abigail R., Schwarz, Marvin I., Evans, Christopher M., Schwartz, David A.
Publicado no Am J Respir Crit Care Med (2016)

STAT3 modulates reprogramming efficiency of human somatic cells; insights from autosomal dominant Hyper IgE syndrome caused by STAT3 mutations

Por Yu, Zhen, Dmitrieva, Natalia I., Walts, Avram D., Jin, Hui, Liu, Yangtengyu, Ping, Xianfeng, Ferrante, Elisa A., Qiu, Lugui, Holland, Steven M., Freeman, Alexandra F., Chen, Guibin, Boehm, Manfred
Publicado no Biol Open (2020)

Stat3-dependent acute Rantes production in vascular smooth muscle cells modulates inflammation following arterial injury in mice

Por Kovacic, Jason C., Gupta, Rohit, Lee, Angela C., Ma, Mingchao, Fang, Fang, Tolbert, Claire N., Walts, Avram D., Beltran, Leilani E., San, Hong, Chen, Guibin, St. Hilaire, Cynthia, Boehm, Manfred
Publicado em 2009

Chronic Hypersensitivity Pneumonitis, an Interstitial Lung Disease with Distinct Molecular Signatures

Por Furusawa, Haruhiko, Cardwell, Jonathan H., Okamoto, Tsukasa, Walts, Avram D., Konigsberg, Iain R., Kurche, Jonathan S., Bang, Tami J., Schwarz, Marvin I., Brown, Kevin K., Kropski, Jonathan A., Rojas, Mauricio, Cool, Carlyne D., Lee, Joyce S., Wolters, Paul J., Yang, Ivana V., Schwartz, David A.
Publicado no Am J Respir Crit Care Med (2020)

MUC5B variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis

Por Mathai, Susan K., Humphries, Stephen M., Kropski, Jonathan A., Blackwell, Timothy S., Powers, Julia, Walts, Avram D., Markin, Cheryl, Woodward, Julia, Chung, Jonathan H., Brown, Kevin K., Steele, Mark P., Loyd, James E., Schwarz, Marvin I., Fingerlin, Tasha E., Yang, Ivana V., Lynch, David A., Schwartz, David A.
Publicado no Thorax (2019)

TGF-β signaling mediates endothelial to mesenchymal transition (EndMT) during vein graft remodeling

Por Cooley, Brian C., Nevado, Jose, Mellad, Jason, Yang, Dan, Hilaire, Cynthia St., Negro, Alejandra, Fang, Fang, Chen, Guibin, San, Hong, Walts, Avram D., Schwartzbeck, Robin L., Taylor, Brandi, Lanzer, Jan D., Wragg, Andrew, Elagha, Abdalla, Beltran, Leilani E., Berry, Colin, Feil, Robert, Virmani, Renu, Ladich, Elena, Kovacic, Jason C., Boehm, Manfred
Publicado em 2014

The relationship between complement C3 expression and the MUC5B genotype in pulmonary fibrosis

Por Okamoto, Tsukasa, Mathai, Susan K., Hennessy, Corinne E., Hancock, Laura A., Walts, Avram D., Stefanski, Adrianne L., Brown, Kevin K., Lynch, David A., Cosgrove, Gregory P., Groshong, Steve D., Cool, Carlyne D., Schwarz, Marvin I., Banda, Nirmal K., Thurman, Joshua M., Yang, Ivana V., Holers, V. Michael, Schwartz, David A.
Publicado no Am J Physiol Lung Cell Mol Physiol (2018)

Flavivirus antagonism of type I interferon signaling reveals prolidase as a regulator of IFNAR1 surface expression

Por Lubick, Kirk J., Robertson, Shelly J., McNally, Kristin L., Freedman, Brett A., Rasmussen, Angela L., Taylor, R. Travis, Walts, Avram D., Tsuruda, Seitaro, Sakai, Mizuki, Ishizuka, Mariko, Boer, Elena F., Foster, Erin C., Chiramel, Abhilash I., Addison, Conrad B., Green, Richard, Kastner, Daniel L., Katze, Michael G., Holland, Steven M., Forlino, Antonella, Freeman, Alexandra F., Boehm, Manfred, Yoshii, Kentaro, Best, Sonja M.
Publicado no Cell Host Microbe (2015)

Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndrome

Por Dmitrieva, Natalia I., Walts, Avram D., Nguyen, Dai Phuong, Grubb, Alex, Zhang, Xue, Wang, Xujing, Ping, Xianfeng, Jin, Hui, Yu, Zhen, Yu, Zu-Xi, Yang, Dan, Schwartzbeck, Robin, Dalgard, Clifton L., Kozel, Beth A., Levin, Mark D., Knutsen, Russell H., Liu, Delong, Milner, Joshua D., López, Diego B., O’Connell, Michael P., Lee, Chyi-Chia Richard, Myles, Ian A., Hsu, Amy P., Freeman, Alexandra F., Holland, Steven M., Chen, Guibin, Boehm, Manfred
Publicado no J Clin Invest (2020)