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Leukemia
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July 1, 1997
Lack of ETV6 (TEL) gene rearrangements or p16INK4A/p15INK4B homozygous gene deletions in infant acute lymphoblastic leukemia
K W Maloney, J E Rubnitz, M L Cleary, et al.
Blood
|
July 15, 1994
Frequency and prognostic significance of HRX rearrangements in infant acute lymphoblastic leukemia: a Pediatric Oncology Group study
J E Rubnitz, M P Link, J J Shuster, et al.
Neoplasia (New York, N.Y.)
|
August 10, 2000
p27KIP1 deletions in childhood acute lymphoblastic leukemia
H Komuro, M B Valentine, J E Rubnitz, et al.
Leukemia
|
June 1, 1996
High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan
D C Liang, T B Chou, J S Chen, et al.
Leukemia
|
April 13, 2011
Impact of genetic variation in FKBP5 on clinical response in pediatric acute myeloid leukemia patients: a pilot study
A K Mitra, K Crews, S Pounds, et al.
Blood
|
June 1, 1996
Molecular analysis of t(11;19) breakpoints in childhood acute leukemias
J E Rubnitz, F G Behm, A M Curcio-Brint, et al.
Blood
|
December 24, 1998
Hyperdiploid acute lymphoblastic leukemia with 51 to 65 chromosomes: a distinct biological entity with a marked propensity to undergo apoptosis
C Ito, M Kumagai, A Manabe, et al.
Leukemia
|
August 11, 1998
Transient encephalopathy following high-dose methotrexate treatment in childhood acute lymphoblastic leukemia
J E Rubnitz, M V Relling, P L Harrison, et al.
Blood
|
February 15, 1997
Case-control study suggests a favorable impact of TEL rearrangement in patients with B-lineage acute lymphoblastic leukemia treated with antimetabolite-based therapy: a Pediatric Oncology Group study
J E Rubnitz, J J Shuster, V J Land, et al.
Leukemia
|
April 14, 2000
Prognostic factors in infants with acute myeloid leukemia
C H Pui, S C Raimondi, D K Srivastava, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 69) with videos related to
Sort By:
Page
of 7
Leukemia
|
July 1, 1997
Lack of ETV6 (TEL) gene rearrangements or p16INK4A/p15INK4B homozygous gene deletions in infant acute lymphoblastic leukemia
K W Maloney, J E Rubnitz, M L Cleary, et al.
Blood
|
July 15, 1994
Frequency and prognostic significance of HRX rearrangements in infant acute lymphoblastic leukemia: a Pediatric Oncology Group study
J E Rubnitz, M P Link, J J Shuster, et al.
Neoplasia (New York, N.Y.)
|
August 10, 2000
p27KIP1 deletions in childhood acute lymphoblastic leukemia
H Komuro, M B Valentine, J E Rubnitz, et al.
Leukemia
|
June 1, 1996
High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan
D C Liang, T B Chou, J S Chen, et al.
Leukemia
|
April 13, 2011
Impact of genetic variation in FKBP5 on clinical response in pediatric acute myeloid leukemia patients: a pilot study
A K Mitra, K Crews, S Pounds, et al.
Blood
|
June 1, 1996
Molecular analysis of t(11;19) breakpoints in childhood acute leukemias
J E Rubnitz, F G Behm, A M Curcio-Brint, et al.
Blood
|
December 24, 1998
Hyperdiploid acute lymphoblastic leukemia with 51 to 65 chromosomes: a distinct biological entity with a marked propensity to undergo apoptosis
C Ito, M Kumagai, A Manabe, et al.
Leukemia
|
August 11, 1998
Transient encephalopathy following high-dose methotrexate treatment in childhood acute lymphoblastic leukemia
J E Rubnitz, M V Relling, P L Harrison, et al.
Blood
|
February 15, 1997
Case-control study suggests a favorable impact of TEL rearrangement in patients with B-lineage acute lymphoblastic leukemia treated with antimetabolite-based therapy: a Pediatric Oncology Group study
J E Rubnitz, J J Shuster, V J Land, et al.
Leukemia
|
April 14, 2000
Prognostic factors in infants with acute myeloid leukemia
C H Pui, S C Raimondi, D K Srivastava, et al.
Page
of 7