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M Emi

Showing results (31-40 of 221) with videos related to

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Nihon Rinsho. Japanese Journal of Clinical Medicine|July 6, 2000
[Methods of single-nucleotide polymorphism analysis and application to hereditary cancer syndrome]I Mikami, H Nagai, H Harada, et al.
Journal of Human Genetics|March 20, 1999
Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the human nuclear factor kappa-beta subunit 1 (NFKB1) locusN Ota, T Nakajima, Y Shirai, et al.
Journal of Human Genetics|December 16, 1998
A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locusK Tsukamoto, N Ohta, Y Shirai, et al.
Nihon Geka Gakkai Zasshi|May 1, 1996
[Genetic alterations and DNA-based diagnosis in breast cancer]S Matsumoto, M Emi, F Kasumi, et al.
Journal of Human Genetics|June 4, 1998
Isolation and mapping of a polymorphic CA repeat sequence at the human interleukin 6 locusK Tsukamoto, K Haruta, T Shiba, et al.
Nucleic Acids Research|September 25, 1990
Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase geneA Hata, M Robertson, M Emi, et al.
Journal of Human Genetics|November 26, 1999
Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) geneT Nakajima, T Hamakubo, T Kodama, et al.
Journal of Human Genetics|July 14, 2001
Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) geneI Nakazawa, T Nakajima, T Ishigami, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 18, 2000
Association of allelic loss on 1q, 4p, 7q, 9p, 9q, and 16q with postoperative death in papillary thyroid carcinomaY Kitamura, K Shimizu, S Tanaka, et al.
Journal of Human Genetics|March 4, 2000
A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL geneK Fukino, A Teramoto, K Adachi, et al.
Pageof 23

Showing results (31-40 of 221) with videos related to

Sort By:
Pageof 23
Nihon Rinsho. Japanese Journal of Clinical Medicine|July 6, 2000
[Methods of single-nucleotide polymorphism analysis and application to hereditary cancer syndrome]I Mikami, H Nagai, H Harada, et al.
Journal of Human Genetics|March 20, 1999
Isolation and radiation hybrid mapping of a highly polymorphic CA repeat sequence at the human nuclear factor kappa-beta subunit 1 (NFKB1) locusN Ota, T Nakajima, Y Shirai, et al.
Journal of Human Genetics|December 16, 1998
A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locusK Tsukamoto, N Ohta, Y Shirai, et al.
Nihon Geka Gakkai Zasshi|May 1, 1996
[Genetic alterations and DNA-based diagnosis in breast cancer]S Matsumoto, M Emi, F Kasumi, et al.
Journal of Human Genetics|June 4, 1998
Isolation and mapping of a polymorphic CA repeat sequence at the human interleukin 6 locusK Tsukamoto, K Haruta, T Shiba, et al.
Nucleic Acids Research|September 25, 1990
Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase geneA Hata, M Robertson, M Emi, et al.
Journal of Human Genetics|November 26, 1999
Genomic structure and chromosomal mapping of the human sterol regulatory element binding protein (SREBP) cleavage-activating protein (SCAP) geneT Nakajima, T Hamakubo, T Kodama, et al.
Journal of Human Genetics|July 14, 2001
Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) geneI Nakazawa, T Nakajima, T Ishigami, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 18, 2000
Association of allelic loss on 1q, 4p, 7q, 9p, 9q, and 16q with postoperative death in papillary thyroid carcinomaY Kitamura, K Shimizu, S Tanaka, et al.
Journal of Human Genetics|March 4, 2000
A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL geneK Fukino, A Teramoto, K Adachi, et al.
Pageof 23