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Showing results (71-80 of 153) with videos related to

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American Journal of Human Genetics|July 1, 1989
Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase geneA Hata, C Setoyama, K Shimada, et al.
Human Genetics|May 1, 1991
A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiencyA Hata, T Matsuura, C Setoyama, et al.
The Journal of Clinical Investigation|March 1, 1994
Angiotensinogen as a risk factor for essential hypertension in JapanA Hata, C Namikawa, M Sasaki, et al.
American Journal of Medical Genetics|June 27, 2000
Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in Japanese womenG Kobashi, H Yamada, T Asano, et al.
American Journal of Clinical Pathology|October 1, 1995
p53 protein expression and p53 gene mutation in thymic epithelial tumors. An immunohistochemical and DNA sequencing studyH Tateyama, T Eimoto, T Tada, et al.
Genes & Development|July 25, 1998
Determinants of specificity in TGF-beta signal transductionY G Chen, A Hata, R S Lo, et al.
American Journal of Human Genetics|October 1, 1990
Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase geneA Hata, M Emi, G Luc, et al.
Biochimica Et Biophysica Acta|October 29, 1985
Assignment of ESR signals of Escherichia coli terminal oxidase complexesA Hata, Y Kirino, K Matsuura, et al.
Seminars in Thrombosis and Hemostasis|January 7, 2000
The factor V Leiden mutation is not a common cause of pregnancy-induced hypertension in JapanG Kobashi, H Yamada, T Asano, et al.
The EMBO Journal|March 15, 1994
Tyrosine kinases Lyn and Syk regulate B cell receptor-coupled Ca2+ mobilization through distinct pathwaysM Takata, H Sabe, A Hata, et al.
Pageof 16

Showing results (71-80 of 153) with videos related to

Sort By:
Pageof 16
American Journal of Human Genetics|July 1, 1989
Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase geneA Hata, C Setoyama, K Shimada, et al.
Human Genetics|May 1, 1991
A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiencyA Hata, T Matsuura, C Setoyama, et al.
The Journal of Clinical Investigation|March 1, 1994
Angiotensinogen as a risk factor for essential hypertension in JapanA Hata, C Namikawa, M Sasaki, et al.
American Journal of Medical Genetics|June 27, 2000
Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in Japanese womenG Kobashi, H Yamada, T Asano, et al.
American Journal of Clinical Pathology|October 1, 1995
p53 protein expression and p53 gene mutation in thymic epithelial tumors. An immunohistochemical and DNA sequencing studyH Tateyama, T Eimoto, T Tada, et al.
Genes & Development|July 25, 1998
Determinants of specificity in TGF-beta signal transductionY G Chen, A Hata, R S Lo, et al.
American Journal of Human Genetics|October 1, 1990
Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase geneA Hata, M Emi, G Luc, et al.
Biochimica Et Biophysica Acta|October 29, 1985
Assignment of ESR signals of Escherichia coli terminal oxidase complexesA Hata, Y Kirino, K Matsuura, et al.
Seminars in Thrombosis and Hemostasis|January 7, 2000
The factor V Leiden mutation is not a common cause of pregnancy-induced hypertension in JapanG Kobashi, H Yamada, T Asano, et al.
The EMBO Journal|March 15, 1994
Tyrosine kinases Lyn and Syk regulate B cell receptor-coupled Ca2+ mobilization through distinct pathwaysM Takata, H Sabe, A Hata, et al.
Pageof 16