Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Dorothy L. Williams"'
Autor:
Gurpreet K. Arora, Arun Gupta, Tong Guo, Aakash Y. Gandhi, Aaron Laine, Dorothy L. Williams, Chul Ahn, Puneeth Iyengar, Rodney E. Infante
Publikováno v:
JCSM Rapid Communications, Vol 3, Iss 2, Pp 115-128 (2020)
Abstract Background Cachexia, a syndrome of muscle atrophy, adipose loss, and anorexia, is associated with reduced survival in cancer patients. The colon adenocarcinoma C26c20 cell line secretes the cytokine leukaemia inhibitory factor (LIF), which i
Externí odkaz:
https://doaj.org/article/4c77e136133e45f4926451ca8c52f173
Autor:
Tong Guo, Chul Ahn, Gurpreet K. Arora, Dorothy L. Williams, Aaron Laine, Aakash Y. Gandhi, Puneeth Iyengar, Rodney E. Infante, Arun Gupta
Publikováno v:
JCSM Rapid Communications, Vol 3, Iss 2, Pp 115-128 (2020)
Background Cachexia, a syndrome of muscle atrophy, adipose loss, and anorexia, is associated with reduced survival in cancer patients. The colon adenocarcinoma C26c20 cell line secretes the cytokine leukaemia inhibitory factor (LIF), which induces ca
Autor:
Tong Guo, Puneeth Iyengar, Dorothy L. Williams, Aakash Y. Gandhi, Rodney E. Infante, Aaron Laine, Chul Ahn, Arun Gupta, Gurpreet K. Arora
BackgroundCachexia (CX), a syndrome of muscle atrophy, adipose loss, and anorexia, is associated with reduced survival in cancer patients. The colon adenocarcinoma C26c20 cell line secretes the cytokine leukemia inhibitor factor (LIF) which induces C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16f048ecb13c3bb2e8e47ddc3a009bf2
https://doi.org/10.1101/2020.01.28.923391
https://doi.org/10.1101/2020.01.28.923391
Autor:
Mark Valentine, William M. Crist, Edwin C. Douglass, Dorothy L. Williams, Susan Lewis, Susana C. Raimondi, Raul C. Ribeiro
Publikováno v:
Leukemia & Lymphoma. 7:401-407
Many fragile sites in the human genome occur at or near chromosomal breakpoints reportedly involved in translocations of DNA material in neoplastic cells. This fact has led some investigators to postulate that fragile sites have a pathogenic role in
Autor:
C H Pui, Dorothy L. Williams, Frederick G. Behm, William M. Crist, Gaston K. Rivera, E. Privitera, A T Look, Susana C. Raimondi
Publikováno v:
Blood. 77:2016-2022
We identified seven new recurring translocations among 483 cases of acute lymphoblastic leukemia (ALL) with adequate chromosome banding studies. Four were apparently balanced [t(1;3)(p34;p21), t(7;9)(p15;p23- p24), t(12;13)(p13;q14), t(17;19)(q22;p13
Autor:
A T Look, Geoffrey R. Kitchingman, Yasuhide Hayashi, Frederick G. Behm, Dorothy L. Williams, Gaston K. Rivera, Susana C. Raimondi, Ching-Hon Pui
Publikováno v:
Blood. 76:1626-1630
To determine the biologic significance of the structural rearrangements of the long arm of chromosome 6(6q) in acute lymphoblastic leukemia (ALL) at diagnosis, we studied 412 consecutive children whose leukemic cell chromosomes had been completely ba
Autor:
C H Pui, A T Look, W M Crist, Dorothy L. Williams, Gaston K. Rivera, Susana C. Raimondi, Frederick G. Behm, Paula K. Roberson
Publikováno v:
Journal of Clinical Oncology. 8:1380-1388
In earlier studies of the cytogenetic characteristics of leukemic lymphoblasts from children with pre-B-cell acute lymphoblastic leukemia (ALL), we concluded that certain chromosomal abnormalities explain, in part, the increased presence of high-risk
Autor:
Ann H. Fuchs, Frederick G. Behm, Yasuhide Hayashi, Geoffrey R. Kitchingman, Susana C. Raimondi, Dorothy L. Williams, Joseph Mirro, Ching-Hon Pui
Publikováno v:
Blood. 76:150-156
The frequency and characteristics of childhood acute leukemia with a 14q32 translocation [other than the t(8;14)(q24;q32)] were determined in 335 cases of newly diagnosed acute lymphoblastic leukemia (ALL) and 105 cases of acute nonlymphoblastic leuk
Autor:
William M. Crist, C H Pui, VJ Land, DJ Pullen, Michael J. Borowitz, Frederick G. Behm, Jonathan J. Shuster, Dorothy L. Williams, Susana C. Raimondi, Andrew J. Carroll
Publikováno v:
Blood. 75:1170-1177
Cytogenetic and DNA flow cytometric analyses of leukemic cells from 2,184 children with newly diagnosed acute lymphoblastic leukemia (ALL) identified 27 cases (1.2%) that had a hypodiploid line with fewer than 45 chromosomes per cell. Had cytogenetic
Autor:
Gary V. Dahl, Michael J. Schell, Dorothy L. Williams, David K. Kalwinsky, Victor M. Santana, Joseph Mirro, Susana C. Raimondi, Frederick G. Behm
Publikováno v:
Journal of Clinical Oncology. 8:75-83
Reports of close associations between recurring chromosomal abnormalities and the clinical behavior of acute nonlymphocytic leukemia (ANLL) have stimulated efforts to define this disease in cytogenetic terms. Here we report on the leukemic cell karyo