Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nicole P. Curtiss"'
Autor:
Brooke M. Emerling, Eric D. Green, Christian P. Kratz, Nicole P. Curtiss, Jason D. Balkman, Jennifer O. Lauchle, Michelle M. Le Beau, Jeannette M. Bonifas, Kevin Shannon
Publikováno v:
Genomics. 85:600-607
Monosomy 7 and deletions of 7q are recurring leukemia-associated cytogenetic abnormalities that correlate with adverse outcomes in children and adults. We describe a 2.52-Mb genomic DNA contig that spans a commonly deleted segment of chromosome band
Autor:
David Stokoe, Elaine Carlson, Kenneth Lieuw, Suzanne Schubbert, Mignon L. Loh, Jeannette M. Bonifas, Jason Gotlib, Peter D. Emanuel, Kevin Shannon, Melissa G. Reynolds, Shashaank Vattikuti, Michelle M. Le Beau, Connie M. Lee, Soheil Meshinchi, Nicole P. Curtiss, Jennifer W. Cheng
Publikováno v:
Blood. 103:2325-2331
The PTPN11 gene encodes SHP-2 (Src homology 2 domain-containing protein tyrosine Phosphatase), a nonreceptor tyrosine protein tyrosine phosphatase (PTPase) that relays signals from activated growth factor receptors to p21Ras (Ras) and other signaling
Autor:
Christian P. Kratz, Lucy E. Side, Richard A. Larson, Kevin Shannon, Michelle M. Le Beau, Pauline W. Wang, Kathryn Teel, Nicole P. Curtiss
Publikováno v:
Genes, chromosomescancer. 39(3)
Oncogenic mutations in the KRAS2, NRAS, or FLT3 gene are detected in more than 50% of patients with de novo acute myeloid leukemia (AML). RAS mutations are also prevalent in de novo myelodysplastic syndrome (MDS), especially chronic myelomonocytic le
Autor:
Lucy E. Side, Nicole P. Curtiss, Kathryn Teel, Christian Kratz, Pauline W. Wang, Richard A. Larson, Michelle M. Le Beau, Kevin M. Shannon
Publikováno v:
Genes, Chromosomes & Cancer; Mar2004, Vol. 39 Issue 3, p217-223, 7p