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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) locus
N 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) locus
K 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 locus
K 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 gene
A 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) gene
T 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) gene
I 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 carcinoma
Y 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 gene
K Fukino, A Teramoto, K Adachi, et al.
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of 23
Search research articles
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Showing results (31-40 of 221) with videos related to
Sort By:
Page
of 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) locus
N 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) locus
K 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 locus
K 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 gene
A 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) gene
T 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) gene
I 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 carcinoma
Y 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 gene
K Fukino, A Teramoto, K Adachi, et al.
Page
of 23