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I Nonaka

Showing results (391-400 of 503) with videos related to

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Brain & Development|December 9, 2000
Siblings of Schwartz-Jampel syndrome with abnormal muscle computed tomographic findingsH Iwata, H Ozawa, A Kamei, et al.
Biochemical and Biophysical Research Communications|November 2, 2001
Correlation of functional and ultrastructural abnormalities of mitochondria in mouse heart carrying a pathogenic mutant mtDNA with a 4696-bp deletionK Nakada, K Inoue, C S Chen, et al.
Journal of Neuroimmunology|May 18, 2000
Haemopoietic biglycan produced by brain cells stimulates growth of microglial cellsA Kikuchi, H Tomoyasu, I Kido, et al.
Life Sciences|March 17, 2006
Irreversible morphological changes in leg bone following chronic gravitational unloading of growing ratsY Ohira, F Kawano, X D Wang, et al.
Lancet (London, England)|June 4, 1994
Diffuse leukodystrophy with a large-scale mitochondrial DNA deletionA Nakai, Y Goto, K Fujisawa, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|May 1, 2018
Enhanced immunity in intradermal vaccination by novel hollow microneedlesN Ogai, I Nonaka, Y Toda, et al.
No to Hattatsu = Brain and Development|July 1, 1995
[Non-Fukuyama type merosin-positive congenital muscular dystrophy with delayed muscle fiber type differentiation: a case report]S Korematsu, O Kobayashi, N Fukushima, et al.
Biochimica Et Biophysica Acta|January 22, 1993
Immunoblot analysis of dystrophin-related protein (DRP)R Koga, S Ishiura, M Takemitsu, et al.
FEBS Letters|November 5, 1997
Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophyY Miyagoe, K Hanaoka, I Nonaka, et al.
No to Hattatsu = Brain and Development|January 1, 1991
[A case with MELAS associated with epilepsia partialis continua]M Miyazaki, T Saijo, K Mori, et al.
Pageof 51

Showing results (391-400 of 503) with videos related to

Sort By:
Pageof 51
Brain & Development|December 9, 2000
Siblings of Schwartz-Jampel syndrome with abnormal muscle computed tomographic findingsH Iwata, H Ozawa, A Kamei, et al.
Biochemical and Biophysical Research Communications|November 2, 2001
Correlation of functional and ultrastructural abnormalities of mitochondria in mouse heart carrying a pathogenic mutant mtDNA with a 4696-bp deletionK Nakada, K Inoue, C S Chen, et al.
Journal of Neuroimmunology|May 18, 2000
Haemopoietic biglycan produced by brain cells stimulates growth of microglial cellsA Kikuchi, H Tomoyasu, I Kido, et al.
Life Sciences|March 17, 2006
Irreversible morphological changes in leg bone following chronic gravitational unloading of growing ratsY Ohira, F Kawano, X D Wang, et al.
Lancet (London, England)|June 4, 1994
Diffuse leukodystrophy with a large-scale mitochondrial DNA deletionA Nakai, Y Goto, K Fujisawa, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|May 1, 2018
Enhanced immunity in intradermal vaccination by novel hollow microneedlesN Ogai, I Nonaka, Y Toda, et al.
No to Hattatsu = Brain and Development|July 1, 1995
[Non-Fukuyama type merosin-positive congenital muscular dystrophy with delayed muscle fiber type differentiation: a case report]S Korematsu, O Kobayashi, N Fukushima, et al.
Biochimica Et Biophysica Acta|January 22, 1993
Immunoblot analysis of dystrophin-related protein (DRP)R Koga, S Ishiura, M Takemitsu, et al.
FEBS Letters|November 5, 1997
Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophyY Miyagoe, K Hanaoka, I Nonaka, et al.
No to Hattatsu = Brain and Development|January 1, 1991
[A case with MELAS associated with epilepsia partialis continua]M Miyazaki, T Saijo, K Mori, et al.
Pageof 51