Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Angela Goodacre"'
Autor:
Ugo Consoli, Shourong Zhao, Albert B. Deisseroth, Susan Escudier, Gisela Sanchez-Williams, Johannes Drach, Angela Goodacre, Agostino Tafuri, Michael Andreeff, Yan-Rong Liu, Doris Drach, Cathleen Dunne, Elihu Estey
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3d1e5386dda87840c48d589186de7b3
https://doi.org/10.1159/000423068
https://doi.org/10.1159/000423068
Autor:
Scott Callaway, Maurice M. Morelock, Angela Goodacre, Michael Thieleking, Casey A. Laris, I. Mikic, David A. Zacharias, Timothy J. Moran, Rodney P. DeLeon, Michael Akong, Susanne Heynen, Edward A. Hunter, Jeffrey H. Price
Publikováno v:
ASSAY and Drug Development Technologies. 3:483-499
This report describes statistical validation methods implemented on assay data for inhibition of subcellular redistribution of nuclear factor kappaB (NF kappaB) in HeLa cells. We quantified cellular inhibition of cytoplasmic-nuclear translocation of
Autor:
Angela Goodacre, Virginia Snell, G. Deng, Albert B. Deisseroth, M. Andreeff, Steve Kornblau, Cynthia M. Lane
Publikováno v:
Molecular Medicine. 4:158-164
Acute myeloid leukemia (AML) is a heterogeneous collection of leukemic disorders ranging from chemotherapy-sensitive subsets [inversion 16 and t(8;21)], which often can be cured with cytosine arabinoside alone, to the most resistant subsets, which ca
Autor:
Susan Escudier, Johannes Drach, Michael Andreeff, Jennifer M. Trujillo, Angela Goodacre, J. M. Pereira-Leahy, H. U. Weier, Michael J. Keating, M. A. Cork
Publikováno v:
Blood. 81:2702-2707
Cytogenetic studies (CG) of 475 chronic lymphocytic leukemia (CLL) cases showed trisomy 12 in 6.1% or 26% of patients with abnormal karyotypes. Fluorescence in situ hybridization (FISH) detected trisomy 12 in 35% of 117 CLL patients. Only 34.6% of ca
Autor:
Nelson G. Ordóñez, Ruth L. Katz, Angela Goodacre, Nina S. Shabb, Cheryl F Hirsch-Ginsberg, Adel K. El-Naggar
Publikováno v:
Cancer. 67:1008-1018
Forty-six fine-needle aspirates of lymphoproliferative lesions from 31 human immunodeficiency virus (HIV)-positive patients were reviewed using cytomorphologic, immunocytochemical, flow cytometric (FCM), cytogenetic, and molecular studies. There were
Autor:
Andrew Rabinovich, John C. Reed, Susanne Heynen, Stanislaw Krajewski, Klaus M. Hahn, Edward A. Hunter, Robert F. Murphy, Angela Goodacre, Jeffrey H. Price, Louis Hodgson
Publikováno v:
Journal of cellular biochemistry. Supplement. 39
Cellular behavior is complex. Successfully understanding systems at ever-increasing complexity is fundamental to advances in modern science and unraveling the functional details of cellular behavior is no exception. We present a collection of prospec
Autor:
Shuwei Jiang, Johannes Drach, Heike Engel, Angela Goodacre, M. Andreeff, Afsaneh Keyhani, Gisela Sanchez-Williams, Nguyen T. Van, Marek Kimmel
Publikováno v:
Leukemia. 13(4)
Detection of karyotypic clonal abnormalities are prognostically useful in patients with acute myelogenous leukemia (AML) and myelodysplastic syndromes (MDS), but cytogenetic methods are not sensitive enough to detect low numbers of residual leukemic
Autor:
Angela Goodacre, Afsaneh Keyhani, Thomas Schenk, S. Bottcher, J. Q. Guo, Hagop M. Kantarjian, Ralph B. Arlinghaus, M. Andreeff, Kay Oliver Kliche
Publikováno v:
Leukemia. 12(5)
Acute lymphocytic leukemia (ALL) is considered a clonal disease restricted to the lymphoid compartment. The Philadelphia chromosome (Ph) is found in a subset of ALL with poor prognosis. Here we present the largest series of Ph+ ALL analyzed for invol
Autor:
Afsaneh Keyhani, Michael Andreeff, Angela Goodacre, Shuwei Jiang, Nguyen T. Van, Gisela Sanchez-Williams, Marek Kimmel, Heike Engel
Publikováno v:
British journal of haematology. 99(1)
The majority of patients with acute myelogenous leukaemia (AML) and myelodysplastic syndromes (MDS) relapse, especially those with unfavourable cytogenetics. This study was designed to investigate the presence and frequency of minimal residual diseas
Autor:
J. L. Palmer, Katharina Clodi, Mark Roberts, Michael Andreeff, Angela Goodacre, Fernando Cabanillas, Anas Younes, Mamoun Younes
Publikováno v:
British journal of haematology. 98(4)
The most common tumour suppressor gene altered in human cancers is p53, which is located on the short arm of chromosome 17. Structural abnormalities of the short arm and loss of chromosome 17 have been reported to confer resistance to chemotherapy in