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Genes, Chromosomes & Cancer
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May 1, 1991
Molecular assignment of a translocation breakpoint in acute myeloid leukemia with t(8;21)
K Shimizu, H Ichikawa, H Miyoshi, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
July 1, 1991
[An 8; 21 chromosome translocation associated leukemia presenting with large intestinal granulocytic sarcoma: a report of two cases]
T Matsunaga, N Maseki, Y Kaneko, et al.
Genes, Chromosomes & Cancer
|
November 20, 1997
Hematologic malignancies with the t(10;11) (p13;q21) have the same molecular event and a variety of morphologic or immunologic phenotypes
H Kobayashi, F Hosoda, N Maseki, et al.
Leukemia
|
June 25, 1998
Amplification of the TCL1 flanking region at 14q32.1 with no TCL1 gene transcription in a patient with peripheral T cell lymphoma
Sakashita, H Kobayashi, N Satake, et al.
Blood
|
August 15, 1993
Junctions of the AML1/MTG8(ETO) fusion are constant in t(8;21) acute myeloid leukemia detected by reverse transcription polymerase chain reaction
T Kozu, H Miyoshi, K Shimizu, et al.
Genes, Chromosomes & Cancer
|
July 1, 1997
Inversion of chromosome 11 inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: identification of a P1 clone spanning the 11q22 breakpoint
H Kobayashi, Y Arai, F Hosoda, et al.
Cancer Research
|
January 1, 1987
Different karyotypic patterns in early and advanced stage neuroblastomas
Y Kaneko, N Kanda, N Maseki, et al.
Leukemia
|
January 1, 1989
Chromosome pattern in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis
Y Kaneko, N Maseki, M Sakurai, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
June 1, 1992
[Malignant lymphoma occurring subsequent to autoimmune disease]
T Matsunaga, N Maseki, Y Kaneko, et al.
Cancer Research
|
December 15, 1992
Consistent disruption of the AML1 gene occurs within a single intron in the t(8;21) chromosomal translocation
K Shimizu, H Miyoshi, T Kozu, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 67) with videos related to
Sort By:
Page
of 7
Genes, Chromosomes & Cancer
|
May 1, 1991
Molecular assignment of a translocation breakpoint in acute myeloid leukemia with t(8;21)
K Shimizu, H Ichikawa, H Miyoshi, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
July 1, 1991
[An 8; 21 chromosome translocation associated leukemia presenting with large intestinal granulocytic sarcoma: a report of two cases]
T Matsunaga, N Maseki, Y Kaneko, et al.
Genes, Chromosomes & Cancer
|
November 20, 1997
Hematologic malignancies with the t(10;11) (p13;q21) have the same molecular event and a variety of morphologic or immunologic phenotypes
H Kobayashi, F Hosoda, N Maseki, et al.
Leukemia
|
June 25, 1998
Amplification of the TCL1 flanking region at 14q32.1 with no TCL1 gene transcription in a patient with peripheral T cell lymphoma
Sakashita, H Kobayashi, N Satake, et al.
Blood
|
August 15, 1993
Junctions of the AML1/MTG8(ETO) fusion are constant in t(8;21) acute myeloid leukemia detected by reverse transcription polymerase chain reaction
T Kozu, H Miyoshi, K Shimizu, et al.
Genes, Chromosomes & Cancer
|
July 1, 1997
Inversion of chromosome 11 inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: identification of a P1 clone spanning the 11q22 breakpoint
H Kobayashi, Y Arai, F Hosoda, et al.
Cancer Research
|
January 1, 1987
Different karyotypic patterns in early and advanced stage neuroblastomas
Y Kaneko, N Kanda, N Maseki, et al.
Leukemia
|
January 1, 1989
Chromosome pattern in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis
Y Kaneko, N Maseki, M Sakurai, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology
|
June 1, 1992
[Malignant lymphoma occurring subsequent to autoimmune disease]
T Matsunaga, N Maseki, Y Kaneko, et al.
Cancer Research
|
December 15, 1992
Consistent disruption of the AML1 gene occurs within a single intron in the t(8;21) chromosomal translocation
K Shimizu, H Miyoshi, T Kozu, et al.
Page
of 7