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Nishino Ichizo
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http://hub.abes.fr/bmj/periodical/ard/2012/volume_71/issue_10/B3506C23F1B54C7BE053120B220AB6A2/authorship/8
http://hub.abes.fr/bmj/periodical/jnnp/2013/volume_84/issue_9/B35A17CA240B5B19E053120B220AE1F6/authorship/8
http://hub.abes.fr/bmj/periodical/jnnp/2013/volume_84/issue_6/B35A17CA23AD5B19E053120B220AE1F6/authorship/2
http://hub.abes.fr/oup/periodical/hmg/2006/volume_15/issue_8/101093hmgddl045/authorship/9
http://hub.abes.fr/oup/periodical/hmg/2009/volume_18/issue_4/101093hmgddn401/authorship/6
http://hub.abes.fr/oup/periodical/hmg/2007/volume_16/issue_2/101093hmgddl446/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2010/volume_19/issue_1/101093hmgddp477/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2007/volume_16/issue_21/101093hmgddm231/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_5/101093hmgddg043/authorship/17
http://hub.abes.fr/oup/periodical/jbchem/2003/volume_133/issue_5/101093jbmvg084/authorship/5
http://hub.abes.fr/oup/periodical/hmg/1995/volume_4/issue_5/101093hmg45807/authorship/14
http://hub.abes.fr/oup/periodical/hmg/2007/volume_16/issue_22/101093hmgddm220/authorship/5
http://hub.abes.fr/oup/periodical/brainj/2006/volume_129/issue_6/101093brainawl077/authorship/10
http://hub.abes.fr/oup/periodical/jbchem/2003/volume_134/issue_1/101093jbmvg113/authorship/6
http://hub.abes.fr/oup/periodical/jbchem/2004/volume_135/issue_6/101093jbmvh086/authorship/7
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Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2
Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in α-dystroglycanopathies
A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy
A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy
Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient mice
Central core disease is due to RYR1 mutations in more than 90% of patients
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease
Expression of ARPP-16/19 in Rat Denervated Skeletal Muscle
Subcellular Localization of Fukutin and Fukutin-Related Protein in Muscle Cells
Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease
A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy
Localization of Calpain 3 in Human Skeletal Muscle and Its Alteration in Limb-Girdle Muscular Dystrophy 2A Muscle
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