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K Ozono

Showing results (61-70 of 88) with videos related to

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Human Molecular Genetics|September 1, 1994
Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotypeN Okamoto, Y Wada, S Ida, et al.
The Journal of Pediatrics|September 20, 2001
Fluorescence in situ hybridization analysis of peripheral blood cells in Pearson marrow-pancreas syndromeI Yanagihara, K Inui, K Yanagihara, et al.
Anesthesiology|December 1, 1990
The inhibitory action of halothane on reflex constriction in mesenteric capacitance veinsT A Stekiel, K Ozono, J B McCallum, et al.
Biochimica Et Biophysica Acta|January 20, 1998
Human galactocerebrosidase gene: promoter analysis of the 5'-flanking region and structural organizationN Sakai, H Fukushima, K Inui, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 6, 2017
Analysis of public discourse on heart transplantation in Japan using social network service dataN Nawa, H Ishida, H Suginobe, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 6, 2000
Genomic organization of the human chondromodulin-1 gene containing a promoter region that confers the expression of reporter gene in chondrogenic ATDC5 cellsI Yanagihara, M Yamagata, N Sakai, et al.
Journal of Human Genetics|April 6, 2001
A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemiaH Hirai, S Nakajima, A Miyauchi, et al.
The Journal of Biological Chemistry|April 8, 1994
Identification of a vitamin D-responsive element in the 5'-flanking region of the rat 25-hydroxyvitamin D3 24-hydroxylase geneY Ohyama, K Ozono, M Uchida, et al.
Journal of Child Neurology|July 5, 2007
Neuronal intranuclear hyaline inclusion disease with rapidly progressive neurological symptomsT Mano, S Takizawa, I Mohri, et al.
Human Mutation|February 12, 2000
A novel mutation of the down-regulated in adenoma gene in a Japanese case with congential chloride diarrhea. Mutations in brief no. 198. OnlineY Etani, S Mushiake, H Tajiri, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|September 1, 1994
Monoallelic expression of normal mRNA in the PIT1 mutation heterozygotes with normal phenotype and biallelic expression in the abnormal phenotypeN Okamoto, Y Wada, S Ida, et al.
The Journal of Pediatrics|September 20, 2001
Fluorescence in situ hybridization analysis of peripheral blood cells in Pearson marrow-pancreas syndromeI Yanagihara, K Inui, K Yanagihara, et al.
Anesthesiology|December 1, 1990
The inhibitory action of halothane on reflex constriction in mesenteric capacitance veinsT A Stekiel, K Ozono, J B McCallum, et al.
Biochimica Et Biophysica Acta|January 20, 1998
Human galactocerebrosidase gene: promoter analysis of the 5'-flanking region and structural organizationN Sakai, H Fukushima, K Inui, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 6, 2017
Analysis of public discourse on heart transplantation in Japan using social network service dataN Nawa, H Ishida, H Suginobe, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 6, 2000
Genomic organization of the human chondromodulin-1 gene containing a promoter region that confers the expression of reporter gene in chondrogenic ATDC5 cellsI Yanagihara, M Yamagata, N Sakai, et al.
Journal of Human Genetics|April 6, 2001
A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemiaH Hirai, S Nakajima, A Miyauchi, et al.
The Journal of Biological Chemistry|April 8, 1994
Identification of a vitamin D-responsive element in the 5'-flanking region of the rat 25-hydroxyvitamin D3 24-hydroxylase geneY Ohyama, K Ozono, M Uchida, et al.
Journal of Child Neurology|July 5, 2007
Neuronal intranuclear hyaline inclusion disease with rapidly progressive neurological symptomsT Mano, S Takizawa, I Mohri, et al.
Human Mutation|February 12, 2000
A novel mutation of the down-regulated in adenoma gene in a Japanese case with congential chloride diarrhea. Mutations in brief no. 198. OnlineY Etani, S Mushiake, H Tajiri, et al.
Pageof 9