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J Nakura

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The Tohoku Journal of Experimental Medicine|December 1, 1991
Substrain comparison of genetically hypertensive rats using DNA fingerprinting, and genetic analysis of blood pressure in the inbred ratsT Katsuya, J Higaki, T Miki, et al.
The Japanese Journal of Human Genetics|December 1, 1993
Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22K Nagano, J Nakura, K Kihara, et al.
Genomics|August 10, 1995
Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mappingL Ye, J Nakura, N Mitsuda, et al.
Human Molecular Genetics|October 1, 1993
Population variation in the dinucleotide repeat polymorphism at the D8S360 locusK Kamino, J Nakura, K Kihara, et al.
Gerontology|January 1, 1993
Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8J Nakura, T Miki, K Nagano, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1989
Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markersY Takemoto, T Miki, J Nakura, et al.
Human Molecular Genetics|February 1, 1994
Dinucleotide repeat polymorphism at D7S813L Ye, J Nakura, T Miki, et al.
The Japanese Journal of Human Genetics|December 1, 1994
Six dinucleotide repeat polymorphisms on chromosome 7J Nakura, T Miki, L Ye, et al.
Journal of Biochemistry|April 1, 1991
Effects of individual mutations in the P-450(C21) pseudogene on the P-450(C21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiencyY Higashi, T Hiromasa, A Tanae, et al.
American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
The Tohoku Journal of Experimental Medicine|December 1, 1991
Substrain comparison of genetically hypertensive rats using DNA fingerprinting, and genetic analysis of blood pressure in the inbred ratsT Katsuya, J Higaki, T Miki, et al.
The Japanese Journal of Human Genetics|December 1, 1993
Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22K Nagano, J Nakura, K Kihara, et al.
Genomics|August 10, 1995
Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mappingL Ye, J Nakura, N Mitsuda, et al.
Human Molecular Genetics|October 1, 1993
Population variation in the dinucleotide repeat polymorphism at the D8S360 locusK Kamino, J Nakura, K Kihara, et al.
Gerontology|January 1, 1993
Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8J Nakura, T Miki, K Nagano, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1989
Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markersY Takemoto, T Miki, J Nakura, et al.
Human Molecular Genetics|February 1, 1994
Dinucleotide repeat polymorphism at D7S813L Ye, J Nakura, T Miki, et al.
The Japanese Journal of Human Genetics|December 1, 1994
Six dinucleotide repeat polymorphisms on chromosome 7J Nakura, T Miki, L Ye, et al.
Journal of Biochemistry|April 1, 1991
Effects of individual mutations in the P-450(C21) pseudogene on the P-450(C21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiencyY Higashi, T Hiromasa, A Tanae, et al.
American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.
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