Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Emma Murad"'
Autor:
Gerald A. Soff, Xianhe Bai, Muhammad Waqas, Traci E. Battle, David A. Frank, Channing J. Der, Masuko Ushio-Fukai, Wolfgang Dubiel, Emma Murad, Keqiang Ye, Francesca Cerimele, Jack L. Arbiser, Paul M. Campbell, Baskaran Govindarajan
Publikováno v:
Journal of Biological Chemistry. 278:35501-35507
Natural products comprise a major source of small molecular weight angiogenesis inhibitors. We have used the transformed endothelial cell line SVR as an effective screen of natural product extracts to isolate anti-angiogenesis and anti-tumor compound
Autor:
Rathnagiri Polavarapu, Jing Shi, Emma Murad, Anne Marie Whalen, Sampath Parthasarathy, J. David Lambeth, Rebecca S. Arnold, John A. Petros, Carrie Q. Sun
Publikováno v:
Proceedings of the National Academy of Sciences. 98:5550-5555
Nox1, a homologue of gp91 phox , the catalytic moiety of the superoxide (O \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \setlength{\oddsid
Autor:
Sareeta Parker, Emma Murad
Publikováno v:
Journal of the American Academy of Dermatology. 62:139-141
Follicular mucinosis is an uncommon inflammatory disorder characterized histologically by mucin accumulation in the follicular epithelium. The condition is generally divided into primary and secondary forms, the latter being frequently associated wit
Autor:
Bahig M. Shehata, Traci E. Battle, Francesca Cerimele, Aristidis Eliopoulos, Emma Murad, Cynthia Cohen, Jack L. Arbiser, John W. Sixbey, Randolph S. Watnick, Rebecca A. Lynch, Ken R. Smith, Nada C. Macaron, David A. Frank
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 102(1)
Burkitt's lymphoma (BL) is an aggressive B cell neoplasm, which is one of the most common neoplasms of childhood. It is highly widespread in East Africa, where it appears in endemic form associated with Epstein–Barr virus (EBV) infection, and aroun
Autor:
Emma Murad, Matthew Nunnelley, Toshiyuki Yamamoto, Francesca Cerimele, William D. Martin, Benjamin Lefkove, Baskaran Govindarajan, Karin Litani, Jack L. Arbiser, Marie Csete, Chunsik Lee, Daniel J. Brat, Cynthia Cohen
Publikováno v:
The Journal of biological chemistry. 280(7)
Tuberous sclerosis (TS) is a common autosomal dominant disorder caused by loss or malfunction of hamartin (tsc1) or tuberin (tsc2). Many lesions in TS do not demonstrate loss of heterozygosity for these genes, implying that dominant negative forms of