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Leukemia
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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
|
June 1, 1993
Human t(1;19)(q23;p13) pre-B acute lymphoblastic leukemia in mice with severe combined immunodeficiency
F M Uckun, J R Downing, R Gunther, et al.
Blood
|
April 1, 1996
Rearrangement of the MLL gene confers a poor prognosis in childhood acute lymphoblastic leukemia, regardless of presenting age
F G Behm, S C Raimondi, J L Frestedt, et al.
Blood
|
December 31, 1997
12p abnormalities and the TEL gene (ETV6) in childhood acute lymphoblastic leukemia
S C Raimondi, S A Shurtleff, J R Downing, 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.
Blood
|
January 15, 1994
The der(11)-encoded MLL/AF-4 fusion transcript is consistently detected in t(4;11)(q21;q23)-containing acute lymphoblastic leukemia
J R Downing, D R Head, S C Raimondi, et al.
Leukemia
|
May 26, 2007
MN1 overexpression is an important step in the development of inv(16) AML
C Carella, J Bonten, S Sirma, et al.
Leukemia
|
December 1, 1995
TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis
S A Shurtleff, A Buijs, F G Behm, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 117) with videos related to
Sort By:
Page
of 12
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
|
June 1, 1993
Human t(1;19)(q23;p13) pre-B acute lymphoblastic leukemia in mice with severe combined immunodeficiency
F M Uckun, J R Downing, R Gunther, et al.
Blood
|
April 1, 1996
Rearrangement of the MLL gene confers a poor prognosis in childhood acute lymphoblastic leukemia, regardless of presenting age
F G Behm, S C Raimondi, J L Frestedt, et al.
Blood
|
December 31, 1997
12p abnormalities and the TEL gene (ETV6) in childhood acute lymphoblastic leukemia
S C Raimondi, S A Shurtleff, J R Downing, 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.
Blood
|
January 15, 1994
The der(11)-encoded MLL/AF-4 fusion transcript is consistently detected in t(4;11)(q21;q23)-containing acute lymphoblastic leukemia
J R Downing, D R Head, S C Raimondi, et al.
Leukemia
|
May 26, 2007
MN1 overexpression is an important step in the development of inv(16) AML
C Carella, J Bonten, S Sirma, et al.
Leukemia
|
December 1, 1995
TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis
S A Shurtleff, A Buijs, F G Behm, et al.
Page
of 12