Zobrazeno 1 - 10
of 46
pro vyhledávání: '"J. R. Downing"'
Publikováno v:
Journal of Virology. 71:2535-2539
The nef gene of the human and simian immunodeficiency viruses (HIV and SIV) encodes a 27 to 34 kDa myristoylated protein that induces downregulation of CD4 from the cell surface and enhances virus infectivity. As shown by experiments on SIV-infected
Autor:
J R, Downing, D R, Head, S C, Raimondi, A J, Carroll, A M, Curcio-Brint, T A, Motroni, M G, Hulshof, D J, Pullen, P H, Domer
Publikováno v:
Blood. 83:330-335
The t(4;11)(q21;q23) is the most common translocation involving band 11q23 and is found predominantly in acute lymphoblastic leukemias (ALLs) of infants. Recent studies have shown that this translocation involves the MLL gene on chromosome 11 and the
Publikováno v:
Methods in molecular medicine. 6
The diagnosis and classification of non-Hodgkin's lymphoma (NHL) has traditionally been made based on morphologic and mununophenotypic criteria. Unfortunately, because of the diverse nature of this group of diseases, rehante solely on these criteria
Publikováno v:
Methods in molecular medicine. 55
The development of modern molecular biology techniques and their use in characterizing the genetic abnormalities that are of pathogenic significance in non-Hodgkin's lymphoma (NHL) now provides a means to diagnose and rationally subcategorize these n
Autor:
J R, Downing
Publikováno v:
Verhandlungen der Deutschen Gesellschaft fur Pathologie. 87
Contemporary treatment of acute leukemia requires the accurate assignment of patients at diagnosis to specific risk groups. To determine whether gene expression profiling could enhance risk assignment, we used oligonucleotide microarrays to analyze t
Publikováno v:
Annals of hematology. 83
The current cure rate of 80% in childhood acute lymphoblastic leukemia (ALL) attests to the effectiveness of risk-directed therapy developed through well-designed clinical trials. The ongoing Total Therapy Study XV at St. Jude Children's Research Hos
Publikováno v:
Genes, chromosomescancer. 30(4)
To determine whether the BCL10 mutation plays a role in the oncogenesis of plasma cell dyscrasias, we used polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP) and direct sequencing analysis and examined the genomic BCL10 muta
Publikováno v:
Leukemia. 13(9)
Publikováno v:
Advances in pediatrics. 45
Molecular genetic determinants of malignant diseases in children are providing insights into the mechanisms of malignancies. These findings have improved diagnosis, treatment, and prognosis.
Autor:
S C, Raimondi, S A, Shurtleff, J R, Downing, J, Rubnitz, S, Mathew, M, Hancock, C H, Pui, G K, Rivera, G C, Grosveld, F G, Behm
Publikováno v:
Blood. 90(11)
Although abnormalities involving the short arm of chromosome 12 (12p) are one of the most frequently observed rearrangements in childhood acute lymphoblastic leukemia (ALL), little is known about the frequency of different structural abnormalities an