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M Tamai

Showing results (201-210 of 411) with videos related to

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Journal of Biochemistry|November 1, 1981
The effect of an in vivo-injected thiol protease inhibitor, E-64-c, on the calcium-induced degeneration of myofilamentsS Ishiura, K Hanada, M Tamai, et al.
Neuropharmacology|December 2, 1998
Characterization of the electrogenic Na+ -K+ pump in bipolar cells isolated from carp retinaI Zushi, M Shimura, M Tamai, et al.
British Heart Journal|September 1, 1976
Diagnosis of endocardial cushion defect with cross-sectional and M-mode scanning echocardiography. Differentiation from secundum atrial septal defectS Beppu, Y Nimura, S Nagata, et al.
Human Pathology|December 1, 1987
Leydig cells within the aspermatogenic seminiferous tubulesH Mori, M Tamai, H Fushimi, et al.
Nature Genetics|July 1, 1995
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in JapaneseS Fuchs, M Nakazawa, M Maw, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1996
Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/RDS geneM Nakazawa, E Kikawa, Y Chida, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 4, 2000
Spontaneous improvement in a case of C1q nephropathyM Nishida, H Kawakatsu, H Komatsu, et al.
Journal of Shoulder and Elbow Surgery|April 18, 2001
Two cases of synovial chondromatosis of the subacromial bursaM Horii, M Tamai, K Kido, et al.
Acta Ophthalmologica Scandinavica|September 16, 2000
Magnetic resonance imaging of a non-pigmented adenoma of the ciliary epitheliumT Nakazawa, T Abe, Y Sato, et al.
Investigative Ophthalmology & Visual Science|August 31, 2001
Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosaY Wada, T Abe, T Takeshita, et al.
Pageof 42

Showing results (201-210 of 411) with videos related to

Sort By:
Pageof 42
Journal of Biochemistry|November 1, 1981
The effect of an in vivo-injected thiol protease inhibitor, E-64-c, on the calcium-induced degeneration of myofilamentsS Ishiura, K Hanada, M Tamai, et al.
Neuropharmacology|December 2, 1998
Characterization of the electrogenic Na+ -K+ pump in bipolar cells isolated from carp retinaI Zushi, M Shimura, M Tamai, et al.
British Heart Journal|September 1, 1976
Diagnosis of endocardial cushion defect with cross-sectional and M-mode scanning echocardiography. Differentiation from secundum atrial septal defectS Beppu, Y Nimura, S Nagata, et al.
Human Pathology|December 1, 1987
Leydig cells within the aspermatogenic seminiferous tubulesH Mori, M Tamai, H Fushimi, et al.
Nature Genetics|July 1, 1995
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in JapaneseS Fuchs, M Nakazawa, M Maw, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1996
Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/RDS geneM Nakazawa, E Kikawa, Y Chida, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 4, 2000
Spontaneous improvement in a case of C1q nephropathyM Nishida, H Kawakatsu, H Komatsu, et al.
Journal of Shoulder and Elbow Surgery|April 18, 2001
Two cases of synovial chondromatosis of the subacromial bursaM Horii, M Tamai, K Kido, et al.
Acta Ophthalmologica Scandinavica|September 16, 2000
Magnetic resonance imaging of a non-pigmented adenoma of the ciliary epitheliumT Nakazawa, T Abe, Y Sato, et al.
Investigative Ophthalmology & Visual Science|August 31, 2001
Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosaY Wada, T Abe, T Takeshita, et al.
Pageof 42