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K Ozono

Showing results (81-90 of 88) with videos related to

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Journal of Neurochemistry|March 1, 1996
Molecular cloning and expression of cDNA for murine galactocerebrosidase and mutation analysis of the twitcher mouse, a model of Krabbe's diseaseN Sakai, K Inui, N Tatsumi, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Analysis of localization of mutated tissue-nonspecific alkaline phosphatase proteins associated with neonatal hypophosphatasia using green fluorescent protein chimerasG Cai, T Michigami, T Yamamoto, et al.
Journal of Periodontal Research|August 27, 2016
Gene therapy improves dental manifestations in hypophosphatasia model miceR Okawa, O Iijima, M Kishino, et al.
Journal of Bone and Mineral Metabolism|August 11, 2001
Hypophosphatemic rickets accompanying McCune-Albright syndrome: evidence that a humoral factor causes hypophosphatemiaT Yamamoto, K I Miyamoto, K Ozono, et al.
Leukemia|August 27, 2011
WT1 peptide vaccination following allogeneic stem cell transplantation in pediatric leukemic patients with high risk for relapse: successful maintenance of durable remissionY Hashii, E Sato-Miyashita, R Matsumura, et al.
Clinical Genetics|April 26, 2008
Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblingsY Miyoshi, M Akagi, A K Agarwal, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 1, 2019
Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfectaY Ohata, S Takeyari, Y Nakano, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 5, 2020
Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfectaY Ohata, S Takeyari, Y Nakano, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Journal of Neurochemistry|March 1, 1996
Molecular cloning and expression of cDNA for murine galactocerebrosidase and mutation analysis of the twitcher mouse, a model of Krabbe's diseaseN Sakai, K Inui, N Tatsumi, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Analysis of localization of mutated tissue-nonspecific alkaline phosphatase proteins associated with neonatal hypophosphatasia using green fluorescent protein chimerasG Cai, T Michigami, T Yamamoto, et al.
Journal of Periodontal Research|August 27, 2016
Gene therapy improves dental manifestations in hypophosphatasia model miceR Okawa, O Iijima, M Kishino, et al.
Journal of Bone and Mineral Metabolism|August 11, 2001
Hypophosphatemic rickets accompanying McCune-Albright syndrome: evidence that a humoral factor causes hypophosphatemiaT Yamamoto, K I Miyamoto, K Ozono, et al.
Leukemia|August 27, 2011
WT1 peptide vaccination following allogeneic stem cell transplantation in pediatric leukemic patients with high risk for relapse: successful maintenance of durable remissionY Hashii, E Sato-Miyashita, R Matsumura, et al.
Clinical Genetics|April 26, 2008
Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblingsY Miyoshi, M Akagi, A K Agarwal, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 1, 2019
Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfectaY Ohata, S Takeyari, Y Nakano, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 5, 2020
Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfectaY Ohata, S Takeyari, Y Nakano, et al.
Pageof 9