D G Gilliland
Overview
Explore the profile of D G Gilliland including associated specialties, affiliations and a list of published articles.
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96
Citations
3960
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Recent Articles
11.
Brown J, Levine R, Thompson C, Basile G, Gilliland D, Freedman A
Leukemia
. 2008 Aug;
22(10):1966-9.
PMID: 18754031
No abstract available.
12.
Quintas-Cardama A, Tong W, Manshouri T, Vega F, Lennon P, Cools J, et al.
Leukemia
. 2008 Apr;
22(6):1117-24.
PMID: 18401417
Amplification of the NUP214-ABL1 oncogene can be detected in patients with T cell acute lymphoblastic leukemia (T-ALL). We screened 29 patients with T cell malignancies for the expression of NUP214-ABL1...
13.
Lasho T, Tefferi A, Hood J, Verstovsek S, Gilliland D, Pardanani A
Leukemia
. 2008 Mar;
22(9):1790-2.
PMID: 18354492
No abstract available.
14.
Pardanani A, Hood J, Lasho T, Levine R, Martin M, Noronha G, et al.
Leukemia
. 2007 Jun;
21(8):1658-68.
PMID: 17541402
JAK2V617F and MPLW515L/K represent recently identified mutations in myeloproliferative disorders (MPD) that cause dysregulated JAK-STAT signaling, which is implicated in MPD pathogenesis. We developed TG101209, an orally bioavailable small molecule...
15.
Tefferi A, Sirhan S, Lasho T, Schwager S, Li C, Dingli D, et al.
Br J Haematol
. 2005 Oct;
131(2):166-71.
PMID: 16197445
Polycythaemia vera (PV) is closely associated with both an acquired activating mutation of the JAK2 tyrosine kinase (JAK2(V617F)) in granulocyte-derived DNA and increased granulocyte polycythaemia rubra vera-1 (PRV-1) expression. In...
16.
Graux C, Cools J, Melotte C, Quentmeier H, Ferrando A, Levine R, et al.
Nat Genet
. 2004 Sep;
36(10):1084-9.
PMID: 15361874
In T-cell acute lymphoblastic leukemia (T-ALL), transcription factors are known to be deregulated by chromosomal translocations, but mutations in protein tyrosine kinases have only rarely been identified. Here we describe...
17.
Stone R, De Angelo J, Galinsky I, Estey E, Klimek V, Grandin W, et al.
Ann Hematol
. 2004 May;
83 Suppl 1:S89-90.
PMID: 15124689
No abstract available.
18.
Gilliland D
Ann Hematol
. 2004 May;
83 Suppl 1:S75-6.
PMID: 15124682
There is still a compelling need to improve therapeutic outcome in AML. However, during the past several years our understanding of the genetic basis of AML, and the nature of...
19.
Vandenberghe P, Wlodarska I, Michaux L, Zachee P, Boogaerts M, Vanstraelen D, et al.
Leukemia
. 2004 Feb;
18(4):734-42.
PMID: 14973504
Detection of the FIP1L1-PDGFRA fusion gene or the corresponding cryptic 4q12 deletion supports the diagnosis of chronic eosinophilic leukemia (CEL) in patients with chronic hypereosinophilia. We retrospectively characterized 17 patients...
20.