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M Oshimura

Showing results (201-210 of 242) with videos related to

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Journal of Medical Genetics|January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndromeJ R Engel, A Smallwood, A Harper, et al.
Molecular and Cellular Biology|May 11, 2000
Telomere maintenance in telomerase-deficient mouse embryonic stem cells: characterization of an amplified telomeric DNAH Niida, Y Shinkai, M P Hande, et al.
Human Molecular Genetics|February 7, 2001
Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genesM Meguro, K Mitsuya, N Nomura, et al.
Cancer Genetics and Cytogenetics|May 1, 1983
A summary of cytogenetic studies on 534 cases of chronic myelocytic leukemia in JapanT Ishihara, M Sasaki, M Oshimura, et al.
Genomics|November 20, 1995
Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1K Kitagawa, X Wang, I Hatada, et al.
Genomics|July 20, 1995
Construction of 110 cosmid markers and a 4.5-Mb YAC contig on human chromosome 8p12-q11A Kurimasa, N Suzuki, S Kumano, et al.
Genomics|August 1, 1992
Assignment of a human DNA double-strand break repair gene (XRCC5) to chromosome 2D J Chen, M S Park, E Campbell, et al.
Oncogene|July 1, 1993
Deletion mapping of chromosome 3p in human uterine cervical cancerT Kohno, H Takayama, M Hamaguchi, et al.
Biochimica Et Biophysica Acta|January 6, 1992
Structure of the human pituitary adenylate cyclase activating polypeptide (PACAP) geneM Hosoya, C Kimura, K Ogi, et al.
Human Molecular Genetics|July 13, 2001
A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitusT Arima, R A Drewell, K L Arney, et al.
Pageof 25

Showing results (201-210 of 242) with videos related to

Sort By:
Pageof 25
Journal of Medical Genetics|January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndromeJ R Engel, A Smallwood, A Harper, et al.
Molecular and Cellular Biology|May 11, 2000
Telomere maintenance in telomerase-deficient mouse embryonic stem cells: characterization of an amplified telomeric DNAH Niida, Y Shinkai, M P Hande, et al.
Human Molecular Genetics|February 7, 2001
Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genesM Meguro, K Mitsuya, N Nomura, et al.
Cancer Genetics and Cytogenetics|May 1, 1983
A summary of cytogenetic studies on 534 cases of chronic myelocytic leukemia in JapanT Ishihara, M Sasaki, M Oshimura, et al.
Genomics|November 20, 1995
Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1K Kitagawa, X Wang, I Hatada, et al.
Genomics|July 20, 1995
Construction of 110 cosmid markers and a 4.5-Mb YAC contig on human chromosome 8p12-q11A Kurimasa, N Suzuki, S Kumano, et al.
Genomics|August 1, 1992
Assignment of a human DNA double-strand break repair gene (XRCC5) to chromosome 2D J Chen, M S Park, E Campbell, et al.
Oncogene|July 1, 1993
Deletion mapping of chromosome 3p in human uterine cervical cancerT Kohno, H Takayama, M Hamaguchi, et al.
Biochimica Et Biophysica Acta|January 6, 1992
Structure of the human pituitary adenylate cyclase activating polypeptide (PACAP) geneM Hosoya, C Kimura, K Ogi, et al.
Human Molecular Genetics|July 13, 2001
A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitusT Arima, R A Drewell, K L Arney, et al.
Pageof 25