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M Ohki

Showing results (131-140 of 199) with videos related to

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Genomics|July 1, 1991
Construction and characterization of a NotI linking library of human chromosome 21A Saito, J P Abad, D N Wang, 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 breakpointH Kobayashi, Y Arai, F Hosoda, et al.
Trends in Genetics : TIG|October 1, 1993
The Runt domain identifies a new family of heteromeric transcriptional regulatorsH Kagoshima, K Shigesada, M Satake, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|June 1, 1985
[Development of a new chromogenic Limulus test specific to endotoxin]T Obayashi, T Kawai, H Tamura, et al.
Progress in Clinical and Biological Research|January 1, 1987
Removal of Limulus test-interfering factors in blood samples with perchloric acid and the improvement of the specificity of the Limulus test by fractionating amebocyte lysateT Obayashi, H Tamura, S Tanaka, et al.
Cancer Research|December 15, 1992
Consistent disruption of the AML1 gene occurs within a single intron in the t(8;21) chromosomal translocationK Shimizu, H Miyoshi, T Kozu, et al.
Cancer Genetics and Cytogenetics|August 25, 1999
Detection of translocation 8;21 on interphase cells from acute myelocytic leukemia by fluorescence in situ hybridization and its clinical applicationK Tanaka, M Arif, H Asou, et al.
Blood|January 7, 1998
Adenoviral E1A-associated protein p300 is involved in acute myeloid leukemia with t(11;22)(q23;q13)K Ida, I Kitabayashi, T Taki, et al.
British Journal of Haematology|December 24, 1997
Genetic analysis of 8;21 chromosomal translocation without AML1 gene involvement in MDS-AMLS Kawano, S Miyanishi, K Shimizu, et al.
British Journal of Haematology|December 1, 1995
Disappearance of AML1-MTG8(ETO) fusion transcript in acute myeloid leukaemia patients with t(8;21) in long-term remissionN Satake, N Maseki, T Kozu, et al.
Pageof 20

Showing results (131-140 of 199) with videos related to

Sort By:
Pageof 20
Genomics|July 1, 1991
Construction and characterization of a NotI linking library of human chromosome 21A Saito, J P Abad, D N Wang, 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 breakpointH Kobayashi, Y Arai, F Hosoda, et al.
Trends in Genetics : TIG|October 1, 1993
The Runt domain identifies a new family of heteromeric transcriptional regulatorsH Kagoshima, K Shigesada, M Satake, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|June 1, 1985
[Development of a new chromogenic Limulus test specific to endotoxin]T Obayashi, T Kawai, H Tamura, et al.
Progress in Clinical and Biological Research|January 1, 1987
Removal of Limulus test-interfering factors in blood samples with perchloric acid and the improvement of the specificity of the Limulus test by fractionating amebocyte lysateT Obayashi, H Tamura, S Tanaka, et al.
Cancer Research|December 15, 1992
Consistent disruption of the AML1 gene occurs within a single intron in the t(8;21) chromosomal translocationK Shimizu, H Miyoshi, T Kozu, et al.
Cancer Genetics and Cytogenetics|August 25, 1999
Detection of translocation 8;21 on interphase cells from acute myelocytic leukemia by fluorescence in situ hybridization and its clinical applicationK Tanaka, M Arif, H Asou, et al.
Blood|January 7, 1998
Adenoviral E1A-associated protein p300 is involved in acute myeloid leukemia with t(11;22)(q23;q13)K Ida, I Kitabayashi, T Taki, et al.
British Journal of Haematology|December 24, 1997
Genetic analysis of 8;21 chromosomal translocation without AML1 gene involvement in MDS-AMLS Kawano, S Miyanishi, K Shimizu, et al.
British Journal of Haematology|December 1, 1995
Disappearance of AML1-MTG8(ETO) fusion transcript in acute myeloid leukaemia patients with t(8;21) in long-term remissionN Satake, N Maseki, T Kozu, et al.
Pageof 20