Ichizo Nishino spends much of his time researching Genetics, Myopathy, Internal medicine, Endocrinology and Mutation. His Myopathy research entails a greater understanding of Pathology. His Pathology course of study focuses on Danon disease and Glycogen storage disease.
The Internal medicine study combines topics in areas such as Nonsense mutation, Respiratory chain, Ullrich congenital muscular dystrophy and Bethlem myopathy. His studies in Endocrinology integrate themes in fields like Collagen VI, Congenital muscular dystrophy and Muscle weakness. His work deals with themes such as Autophagosome membrane, Neuroscience and Autophagosome maturation, which intersect with Bioinformatics.
His main research concerns Pathology, Myopathy, Internal medicine, Genetics and Muscular dystrophy. His Pathology research includes elements of Muscle weakness and Skeletal muscle. His study looks at the relationship between Skeletal muscle and fields such as Cell biology, as well as how they intersect with chemical problems.
His studies deal with areas such as Rimmed vacuoles, Hereditary inclusion body myopathy, Anatomy, Danon disease and Disease as well as Myopathy. The concepts of his Internal medicine study are interwoven with issues in Gastroenterology, Endocrinology and Cardiology. His Muscular dystrophy study incorporates themes from Limb-girdle muscular dystrophy and Duchenne muscular dystrophy.
His primary areas of study are Pathology, Internal medicine, Myopathy, Muscle biopsy and Muscular dystrophy. Ichizo Nishino has researched Pathology in several fields, including Mutation, Phenotype and Antibody. His Mutation research integrates issues from Congenital muscular dystrophy and Cell biology.
His study in Internal medicine is interdisciplinary in nature, drawing from both Gastroenterology, Endocrinology and Cardiology. The study incorporates disciplines such as Pathological, Nemaline bodies, Respiratory failure, Disease and Weakness in addition to Myopathy. His Muscular dystrophy study is concerned with the field of Genetics as a whole.
Ichizo Nishino mostly deals with Pathology, Myopathy, Muscular dystrophy, Internal medicine and Muscle biopsy. He works in the field of Pathology, namely Myositis. His Myopathy research incorporates elements of Danon disease, Hypertrophic cardiomyopathy and Chaperone, Cell biology.
His work carried out in the field of Muscular dystrophy brings together such families of science as Phenotype, Biceps, Nonsense and Exon. His research in Internal medicine intersects with topics in Gastroenterology, Endocrinology, Facial Muscle Weakness and Genotype. Ichizo Nishino has included themes like Dermatomyositis and Neurology in his Muscle biopsy study.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Guidelines for the use and interpretation of assays for monitoring autophagy
Daniel J. Klionsky;Fabio C. Abdalla;Hagai Abeliovich;Robert T. Abraham.
Autophagy (2012)
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin.
Autophagy (2016)
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes
Daniel J. Klionsky;Hagai Abeliovich;Patrizia Agostinis;Devendra K. Agrawal.
Autophagy (2008)
Thymidine Phosphorylase Gene Mutations in MNGIE, a Human Mitochondrial Disorder
Ichizo Nishino;Antonella Spinazzola;Michio Hirano.
Science (1999)
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
Ichizo Nishino;Jin Fu;Kurenai Tanji;Takeshi Yamada.
Nature (2000)
Adiponectin and AdipoR1 regulate PGC-1alpha and mitochondria by Ca(2+) and AMPK/SIRT1.
Masato Iwabu;Toshimasa Yamauchi;Miki Okada-Iwabu;Koji Sato.
Nature (2010)
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin.
Parasites & Vectors (2016)
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies
Daniel E. Michele;Rita Barresi;Motoi Kanagawa;Fumiaki Saito.
Nature (2002)
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
L C Papadopoulou;C M Sue;M M Davidson;K Tanji.
Nature Genetics (1999)
Skeletal Muscle FOXO1 (FKHR) Transgenic Mice Have Less Skeletal Muscle Mass, Down-regulated Type I (Slow Twitch/Red Muscle) Fiber Genes, and Impaired Glycemic Control
Yasutomi Kamei;Shinji Miura;Miki Suzuki;Yuko Kai.
Journal of Biological Chemistry (2004)
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