Search Results - "Kalra, Ruby"

Monosomy 7 and Activating RAS Mutations Accompany Malignant Transformation in Patients With Congenital Neutropenia by Kalra, Ruby, Dale, David, Freedman, Melvin, Bonilla, Mary Ann, Weinblatt, Mark, Ganser, Arnold, Bowman, Paul, Abish, Sharon, Priest, Jack, Oseas, Ronald S., Olson, Kristin, Paderanga, Dorothy, Shannon, Kevin

“…Individuals with severe forms of congenital neutropenia suffer from recurrent infections. The therapeutic use of recombinant human granulocyte…”
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Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas by von Haken, Markus S., White, Eileen C., Daneshvar-Shyesther, Laleh, Sih, Sharon, Choi, Eugene, Kalra, Ruby, Cogen, Philip H.

“…Ependymomas are glial tumors of the brain and spinal cord occurring both sporadically and in a familial syndrome, neurofibromatosis type 2 (NF2). Previous…”
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Genetic Analysis Is Consistent With the Hypothesis That NF1 Limits Myeloid Cell Growth Through p21ras by Kalra, Ruby, Paderanga, Dorothy C., Olson, Kristin, Shannon, Kevin M.

“…Children with neurofibromatosis, type 1 (NF-1) are at increased risk of developing malignant myeloid disorders and their bone marrows frequently show loss of…”
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