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T Arinami

Showing results (31-40 of 136) with videos related to

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Human Genetics|August 1, 1987
Frequency of the fragile X syndrome in institutionalized mentally retarded females in JapanT Arinami, I Kondo, S Nakajima, et al.
Neuroscience Letters|December 8, 2000
Mutation analysis of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) in schizophreniaK Sakurai, M Toru, K Yamakawa-Kobayashi, et al.
American Journal of Human Genetics|February 11, 1999
Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26H Ikeda, T Sasaki, T Yoshimoto, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 22, 1999
The 5' region of the tryptophan hydroxylase gene: mutation search and association study with alcoholismH Ishiguro, T Saito, H Shibuya, et al.
Neurology|November 1, 1996
The 5-repeat allele in the very-low-density lipoprotein receptor gene polymorphism is not increased in sporadic Alzheimer's disease in JapaneseT Arinami, K Takekoshi, H Yanagi, et al.
Human Genetics|June 1, 1990
Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3----qter)T Arinami, T Hirano, K Kobayashi, et al.
Human Genetics|November 1, 1993
Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutateT Arinami, M Asano, K Kobayashi, et al.
Psychiatric Genetics|June 13, 1998
Systematic search for mutations in the 14-3-3 eta chain gene on chromosome 22 in schizophrenicsT Hayakawa, H Ishiguro, M Toru, et al.
Human Genetics|September 1, 1987
A fragile X female with Down syndromeT Arinami, I Kondo, H Hamaguchi, et al.
Psychiatry Research|April 29, 1999
No association between C-45T polymorphism in the Sp1 binding site of the promoter region of the cholecystokinin gene and alcoholismH Ishiguro, T Saito, H Shibuya, et al.
Pageof 14

Showing results (31-40 of 136) with videos related to

Sort By:
Pageof 14
Human Genetics|August 1, 1987
Frequency of the fragile X syndrome in institutionalized mentally retarded females in JapanT Arinami, I Kondo, S Nakajima, et al.
Neuroscience Letters|December 8, 2000
Mutation analysis of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) in schizophreniaK Sakurai, M Toru, K Yamakawa-Kobayashi, et al.
American Journal of Human Genetics|February 11, 1999
Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26H Ikeda, T Sasaki, T Yoshimoto, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 22, 1999
The 5' region of the tryptophan hydroxylase gene: mutation search and association study with alcoholismH Ishiguro, T Saito, H Shibuya, et al.
Neurology|November 1, 1996
The 5-repeat allele in the very-low-density lipoprotein receptor gene polymorphism is not increased in sporadic Alzheimer's disease in JapaneseT Arinami, K Takekoshi, H Yanagi, et al.
Human Genetics|June 1, 1990
Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3----qter)T Arinami, T Hirano, K Kobayashi, et al.
Human Genetics|November 1, 1993
Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutateT Arinami, M Asano, K Kobayashi, et al.
Psychiatric Genetics|June 13, 1998
Systematic search for mutations in the 14-3-3 eta chain gene on chromosome 22 in schizophrenicsT Hayakawa, H Ishiguro, M Toru, et al.
Human Genetics|September 1, 1987
A fragile X female with Down syndromeT Arinami, I Kondo, H Hamaguchi, et al.
Psychiatry Research|April 29, 1999
No association between C-45T polymorphism in the Sp1 binding site of the promoter region of the cholecystokinin gene and alcoholismH Ishiguro, T Saito, H Shibuya, et al.
Pageof 14