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M Kunishige

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Muscle & Nerve|July 1, 1995
Mitochondrial encephalomyopathy with autosomal dominant inheritance: a clinical and genetic entity of mitochondrial diseasesH Kawai, M Akaike, K Yokoi, et al.
Angiology|March 1, 1997
Interferon alpha-2a therapy for disseminated intravascular coagulation in a patient with blue rubber bleb nevus syndrome. A case reportM Kunishige, H Azuma, K Masuda, et al.
Journal of the Neurological Sciences|July 1, 1996
Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathiesT Mitsui, H Kawai, M Nagasawa, et al.
Journal of Cellular Biochemistry|April 20, 2000
Functional association between nicotinic acetylcholine receptor and sarcomeric proteins via actin and desmin filamentsT Mitsui, M Kawajiri, M Kunishige, et al.
Clinical Cardiology|March 1, 1997
Cardiac dysfunction in patients with chronic progressive external ophthalmoplegiaM Akaike, H Kawai, K Yokoi, et al.
Journal of the Neurological Sciences|February 10, 1998
New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiencyI Higuchi, H Iwaki, H Kawai, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 1, 1995
Graves' disease in HTLV-I carriersH Kawai, K Yokoi, M Akaike, et al.
Environmental and Molecular Mutagenesis|October 26, 1999
Spontaneous mutation frequency and pattern in Big Blue mice fed a vitamin E-supplemented dietS R Moore, K A Hill, P W Heinmoller, et al.
Mutation Research|February 13, 2001
Mutation frequency is reduced in the cerebellum of Big Blue mice overexpressing a human wild type SOD1 geneM Kunishige, K A Hill, A M Riemer, et al.
Muscle & Nerve|October 15, 1998
Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese familiesH Kawai, M Akaike, M Kunishige, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Muscle & Nerve|July 1, 1995
Mitochondrial encephalomyopathy with autosomal dominant inheritance: a clinical and genetic entity of mitochondrial diseasesH Kawai, M Akaike, K Yokoi, et al.
Angiology|March 1, 1997
Interferon alpha-2a therapy for disseminated intravascular coagulation in a patient with blue rubber bleb nevus syndrome. A case reportM Kunishige, H Azuma, K Masuda, et al.
Journal of the Neurological Sciences|July 1, 1996
Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathiesT Mitsui, H Kawai, M Nagasawa, et al.
Journal of Cellular Biochemistry|April 20, 2000
Functional association between nicotinic acetylcholine receptor and sarcomeric proteins via actin and desmin filamentsT Mitsui, M Kawajiri, M Kunishige, et al.
Clinical Cardiology|March 1, 1997
Cardiac dysfunction in patients with chronic progressive external ophthalmoplegiaM Akaike, H Kawai, K Yokoi, et al.
Journal of the Neurological Sciences|February 10, 1998
New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiencyI Higuchi, H Iwaki, H Kawai, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 1, 1995
Graves' disease in HTLV-I carriersH Kawai, K Yokoi, M Akaike, et al.
Environmental and Molecular Mutagenesis|October 26, 1999
Spontaneous mutation frequency and pattern in Big Blue mice fed a vitamin E-supplemented dietS R Moore, K A Hill, P W Heinmoller, et al.
Mutation Research|February 13, 2001
Mutation frequency is reduced in the cerebellum of Big Blue mice overexpressing a human wild type SOD1 geneM Kunishige, K A Hill, A M Riemer, et al.
Muscle & Nerve|October 15, 1998
Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese familiesH Kawai, M Akaike, M Kunishige, et al.
Pageof 2