Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mary Haughey"'
Autor:
Ivan O. Rosas, Souheil El-Chemaly, Patricia Julien-Williams, Mary Haughey, Ye Cui, Angelo M. Taveira-DaSilva, Hilary J. Goldberg, Amanda M. Jones, Rie Maurer, Don C. Bienfang, Elizabeth Peters, Joel Moss, Shefali Bagwe, Elizabeth P. Henske, Julian A. Villalba
Publikováno v:
Chest. 151:1302-1310
Background Animal and cellular studies support the importance of autophagy inhibition in lymphangioleiomyomatosis (LAM). In a cohort of subjects with LAM, we tested the hypothesis that treatment with sirolimus and hydroxychloroquine (an autophagy inh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0df37120e14b2769a9df4c19b4ad42ca
https://doi.org/10.1016/j.chest.2017.01.033
https://doi.org/10.1016/j.chest.2017.01.033
Autor:
Joel Moss, Shaowei Li, Mary Haughey, Edward W. Cowen, Ji-an Wang, Thomas N. Darling, Neera R. Nathan
Publikováno v:
Journal of the American Academy of Dermatology. 73:802-808
Background Oral mechanistic target of rapamycin inhibitors have been shown to reduce visceral tumor volume in patients with tuberous sclerosis complex (TSC). Objective We sought to evaluate the cutaneous response to oral sirolimus in patients with TS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc72493b37e526c2aa2bbbe2499e7835
https://doi.org/10.1016/j.jaad.2015.07.018
https://doi.org/10.1016/j.jaad.2015.07.018
Autor:
Patricia Julien-Williams, Connie G. Glasgow, Wendy K. Steagall, Mario Stylianou, Mary Haughey, Gustavo Pacheco-Rodriguez, Bernadette R. Gochuico, Joel Moss
Publikováno v:
Chest. 153(2)
Background Lymphangioleiomyomatosis (LAM) is a destructive lung disease of women caused by proliferation of neoplastic-like LAM cells, with mutations in the TSC1/2 tumor suppressor genes. Based on case reports, levels of cancer antigen 125 (CA-125),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d5bc4a010bb4c72b99d4d293fcb703c
https://pubmed.ncbi.nlm.nih.gov/29406212
https://pubmed.ncbi.nlm.nih.gov/29406212
Autor:
Suowen Xu, J. Philip McCoy, Gustavo Pacheco-Rodriguez, Joel Moss, Mario Stylianou, Mary Haughey, Thomas N. Darling, Hai-Ping Wu, Xiong Cai, Leigh Samsel
Publikováno v:
Chest. 145:108-112
Background Lymphangioleiomyomatosis (LAM), sporadic or in women with tuberous sclerosis complex (TSC), is characterized by cystic lung destruction, lymphatic involvement (eg, chylous pleural effusions, lymphangioleiomyomas), and renal angiomyolipomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8767e46eaa2705152537bab484dd668a
https://doi.org/10.1378/chest.13-1071
https://doi.org/10.1378/chest.13-1071
Autor:
Souheil El-Chemaly, Gustavo Pacheco-Rodriguez, J. Philip McCoy, Mary Haughey, Joel Moss, Wendy K. Steagall, Jing-Ping Lin, Qingyuan Fan, Leigh Samsel, Xiong Cai, Thomas N. Darling, Hai-Ping Wu
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 182:1410-1418
Lymphangioleiomyomatosis (LAM), occurring sporadically (S-LAM) or in patients with tuberous sclerosis complex (TSC), results from abnormal proliferation of LAM cells exhibiting mutations or loss of heterozygosity (LOH) of the TSC genes, TSC1 or TSC2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90b27bbf8ec33c5afd411c6c7fc2080f
https://doi.org/10.1164/rccm.201003-0489oc
https://doi.org/10.1164/rccm.201003-0489oc
Autor:
Mary Haughey, Joel Moss, Jiro Kato, Gustavo Pacheco-Rodriguez, Vincent C. Manganiello, Li Zhang, Joseph R. Fontana, Wendy K. Steagall
Publikováno v:
American journal of respiratory and critical care medicine. 191(3)
To the Editor: Lymphangioleiomyomatosis (LAM) is a rare multisystem disease affecting primarily women. It is characterized by cystic lung destruction, lymphatic infiltration, and renal angiomyolipomas, resulting from proliferation of smooth muscle-li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6b28b7e73fd28db5bf4ad30298a0068
https://pubmed.ncbi.nlm.nih.gov/25635494
https://pubmed.ncbi.nlm.nih.gov/25635494
Autor:
Joel Moss, Wendy K. Steagall, Thomas V. Colby, Jiro Kato, Mary Haughey, Gustavo Pacheco-Rodriguez, Li Zhang
Publikováno v:
European Respiratory Journal. 50:1700521
Detection of BRAF and NRAS in Langerhans-like cells from a patient with pulmonary Langerhans9 cell histiocytosishttp://ow.ly/cCDG30f0TcT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::507b65c1ce4c5326d9675dc6b1de8fc2
https://doi.org/10.1183/13993003.00521-2017
https://doi.org/10.1183/13993003.00521-2017
Autor:
Bernadette R. Gochuico, Mary Haughey, Nathan R. Peterson, Kirkland Wilson, Hai Ping Wu, Rodrigo T. Calado, Joel Moss, Neal S. Young, Shira G. Ziegler, William A. Gahl, Souheil El-Chemaly
Previous studies have identified subclinical lung disease in family members of probands with familial pulmonary fibrosis, but the natural history of preclinical pulmonary fibrosis is uncertain. The purpose of this study was to determine whether indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::225670d12b2e0598e8316d7ab6de756a
https://europepmc.org/articles/PMC3087459/
https://europepmc.org/articles/PMC3087459/
Publikováno v:
Journal of the American Society of Nephrology : JASN. 7(3)
The vasopressin-sensitive water channel (aquaporin 2; AQP-2) mediates water transport across the apical plasma membrane of the renal collecting ducts and is excreted in human urine. This study presents the hypothesis that measurements of the AQP-2 ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55c39ca3e9c998853d3022cbf1391178
https://pubmed.ncbi.nlm.nih.gov/8704105
https://pubmed.ncbi.nlm.nih.gov/8704105