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M Owada

Showing results (111-120 of 119) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1982
Cherry-red spot--myoclonus syndrome in a Japanese familyT Kitagawa, M Owada, T Sakiyama, et al.
Enzyme|January 1, 1987
Treatment of phenylketonuria with a formula consisting of low-phenylalanine peptide. A collaborative studyT Kitagawa, M Owada, K Aoki, et al.
Hypertension (Dallas, Tex. : 1979)|February 4, 1999
Involvement of PYK2 in angiotensin II signaling of vascular smooth muscle cellsS Eguchi, H Iwasaki, T Inagami, et al.
Biochemical and Biophysical Research Communications|August 1, 1982
Elevation of nucleotide pyrophosphatase activity in skin fibroblasts from patients with Lowe's syndromeH Yoshida, S Fukui, I Yamashina, et al.
Hypertension (Dallas, Tex. : 1979)|April 30, 2003
Selective involvement of p130Cas/Crk/Pyk2/c-Src in endothelin-1-induced JNK activationHiroaki Kodama, Keiichi Fukuda, Eiichi Takahashi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1997
6-Pyruvoyl-tetrahydropterin synthase deficiency with generalized dystonia and diurnal fluctuation of symptoms: a clinical and molecular studyT Hanihara, K Inoue, C Kawanishi, et al.
Human Genetics|October 28, 1997
Molecular analysis of dihydropteridine reductase deficiency: identification of two novel mutations in Japanese patientsH Ikeda, Y Matsubara, H Mikami, et al.
The Journal of Biological Chemistry|May 16, 1998
Calcium-dependent epidermal growth factor receptor transactivation mediates the angiotensin II-induced mitogen-activated protein kinase activation in vascular smooth muscle cellsS Eguchi, K Numaguchi, H Iwasaki, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Enzyme replacement therapy in Japanese Fabry disease patients: the results of a phase 2 bridging studyY Eto, T Ohashi, Y Utsunomiya, et al.
Pageof 12

Showing results (111-120 of 119) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 119 results.
Journal of Inherited Metabolic Disease|January 1, 1982
Cherry-red spot--myoclonus syndrome in a Japanese familyT Kitagawa, M Owada, T Sakiyama, et al.
Enzyme|January 1, 1987
Treatment of phenylketonuria with a formula consisting of low-phenylalanine peptide. A collaborative studyT Kitagawa, M Owada, K Aoki, et al.
Hypertension (Dallas, Tex. : 1979)|February 4, 1999
Involvement of PYK2 in angiotensin II signaling of vascular smooth muscle cellsS Eguchi, H Iwasaki, T Inagami, et al.
Biochemical and Biophysical Research Communications|August 1, 1982
Elevation of nucleotide pyrophosphatase activity in skin fibroblasts from patients with Lowe's syndromeH Yoshida, S Fukui, I Yamashina, et al.
Hypertension (Dallas, Tex. : 1979)|April 30, 2003
Selective involvement of p130Cas/Crk/Pyk2/c-Src in endothelin-1-induced JNK activationHiroaki Kodama, Keiichi Fukuda, Eiichi Takahashi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1997
6-Pyruvoyl-tetrahydropterin synthase deficiency with generalized dystonia and diurnal fluctuation of symptoms: a clinical and molecular studyT Hanihara, K Inoue, C Kawanishi, et al.
Human Genetics|October 28, 1997
Molecular analysis of dihydropteridine reductase deficiency: identification of two novel mutations in Japanese patientsH Ikeda, Y Matsubara, H Mikami, et al.
The Journal of Biological Chemistry|May 16, 1998
Calcium-dependent epidermal growth factor receptor transactivation mediates the angiotensin II-induced mitogen-activated protein kinase activation in vascular smooth muscle cellsS Eguchi, K Numaguchi, H Iwasaki, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Enzyme replacement therapy in Japanese Fabry disease patients: the results of a phase 2 bridging studyY Eto, T Ohashi, Y Utsunomiya, et al.
Pageof 12