Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Lyska, Emerson"'
Autor:
Thai H. Ho, Kenneth M. Boucher, Timothy Sargis, Jeffrey Mohlman, Deepika Sirohi, Christopher G. Wood, Adela Ramirez-Torres, Archana M. Agarwal, Lyska Emerson, Neeraj Agarwal, Pheroze Tamboli, Benjamin T. Spike, Rebecca S. S. Tidwell, Benjamin L. Maughan, Guillermina Garcia, Eric Jonasch, Sophie Cowman, Sheryl R. Tripp, Adam A. Olalde, Christopher J. Conley, Mei Yee Koh, Miekan A Stonhill, Neelima Kandula, Xian De Liu, Kanishka Sircar, Daniel Fuja, Jose A. Karam
Publikováno v:
Clin Cancer Res
Purpose: Clear cell renal cell carcinoma (ccRCC) is frequently associated with inactivation of the von Hippel–Lindau tumor suppressor, resulting in activation of HIF-1α and HIF-2α. The current paradigm, established using mechanistic cell-based st
Autor:
William T. Couldwell, Yair M. Gozal, Evan Joyce, Jason P. Hunt, Hussam Abou-Al-Shaar, Clough Shelton, Lyska Emerson
Publikováno v:
Journal of Neurosurgery. 131:109-113
Jugular foramen cavernous hemangiomas are extremely rare vascular malformations, and, to the best of the authors’ knowledge, their occurrence as multifocal lesions involving both intra- and extracranial compartments has never been reported before.
Publikováno v:
International Journal of Surgical Pathology. 27:294-304
Cribriform-morular variant of papillary thyroid carcinoma (CMVPTC) is usually an inherited malignancy and may be a presenting indicator of familial adenomatous polyposis syndrome although it may occasionally be sporadic. Known CMVPTC mutations includ
Autor:
Lyska Emerson, Tanmay S. Panchabhai, Brandon T. Larsen, Earle S. Collum, Erinn Downs-Kelly, Katherine E. Boylan, Leif Jensen, Brittany A. Young
Publikováno v:
International Journal of Surgical Pathology. 26:629-634
Mycobacterial spindle cell pseudotumor (MSP) is a rare benign spindle cell lesion containing acid-fact mycobacteria. These lesions are most commonly identified in the lymph nodes, skin, spleen, or bone marrow of immunocompromised patients and only ra
Publikováno v:
Clinical Medicine Insights: Pathology, Vol 1 (2008)
Cytokeratin expression has been documented in a variety of sarcomas including synovial sarcomas, epithelioid sarcomas, Ewing's sarcomas and, rarely, osteosarcomas. In osteosarcomas immunohistochemically shown to expression cytokeratins, a component o
Externí odkaz:
https://doaj.org/article/e4c1b6451b074c259d4ab0aa90ea8095
Autor:
Kenneth M. Boucher, Sophie Cowman, Jose A. Karam, Guillermina Garcia, Rebecca S. S. Tidwell, Xian De Liu, Thai H. Ho, Lyska Emerson, Eric Jonasch, Adam A. Olalde, Neelima Kandula, Christopher G. Wood, Adela Ramirez-Torres, Pheroze Tamboli, Daniel Fuja, Jeffrey Mohlman, Kanishka Sircar, Miekan A Stonhill, Timothy Sargis, Neeraj Agarwal, Benjamin L. Maughan, Archana M. Agarwal, Deepika Sirohi, Sheryl R. Tripp, Christopher J. Conley, Mei Yee Koh, Benjamin T. Spike
Publikováno v:
Clinical Cancer Research. 27:3265-3265
In the original version of [this article][1] ([1][2]), the wrong files were supplied for Figs. 5B and C. The figures and related article text have been corrected in the latest online HTML and PDF versions of this article. The authors regret these err
Autor:
Emily Eckman, Lyska Emerson, John R. Hoidal, Mary-Beth Scholand, Kael F. Fischer, John D. Kriesel
Publikováno v:
Open Forum Infectious Diseases
Background Sarcoidosis is an autoimmune disease characterized by granulomatous lung disease with very prominent mediastinal adenopathy. Acid-fast bacteria, fungi, and viruses have been considered as possible causes of sarcoidosis. We used next-genera
Autor:
Cook George W, Denise Raterman, Lyska Emerson, Michael G. Benton, William J Rowell, Primo Baybayan, Daniel Burgess, Jenny Gu, Heath D. Herbold, Thomas K. Varghese, John M. O’Shea, Cynthia Moehlenkamp, George F. Mayhew, Wallace Akerley, Christine C. Lambert, John T. Fussell, Kevin Eng
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0226340 (2020)
PLoS ONE
PLoS ONE
Structural variation (SV) is typically defined as variation within the human genome that exceeds 50 base pairs (bp). SV may be copy number neutral or it may involve duplications, deletions, and complex rearrangements. Recent studies have shown SV to
Autor:
Martin J. Heslin, Manisha H. Shah, Deborah A. Freedman-Cass, James C. Yao, Paul T. Fanta, Fouad Kandeel, Whitney S. Goldner, Julie Ann Sosa, Gitonga Munene, Venu G. Pillarisetty, Christopher H. Lieu, Boris W. Kuvshinoff, Pamela L. Kunz, Jeffrey F. Moley, Jean Nicolas Vauthey, Thorvardur R. Halfdanarson, Leonard B. Saltz, Jordan Berlin, Paul F. Engstrom, Jennifer L. Burns, Matthew H. Kulke, Emily K. Bergsland, Lyska Emerson, Al B. Benson, Thomas J. Giordano, Lawrence S. Blaszkowsky, Christopher L. Wolfgang, Jonathan R. Strosberg
Publikováno v:
Scopus-Elsevier
Neuroendocrine tumors (NETs) comprise a broad family of tumors that may or may not be associated with symptoms attributable to hormonal hypersecretion. The NCCN Clinical Practice Guidelines in Oncology for Neuroendocrine Tumors discuss the diagnosis
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-3 (2017)
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-3 (2017)
Background Eosinophilic granulomatosis with polyangiitis is a rare, necrotizing systemic vasculitis associated with asthma and hypereosinophilia. Its cause and pathophysiology are still being elucidated. Case presentation We report a case of eosinoph