His main research concerns Genetics, Sarcoglycan, Dystrophin, Muscular dystrophy and Sarcoglycanopathy. The concepts of his Genetics study are interwoven with issues in Molecular biology and Malignant hyperthermia. His Molecular biology study combines topics in areas such as Rimmed vacuoles, Hereditary inclusion body myopathy, Vacuole and Myopathy.
Satoru Noguchi focuses mostly in the field of Muscular dystrophy, narrowing it down to matters related to Gene mutation and, in some cases, Missense mutation, Congenital muscular dystrophy, Fukutin, Internal medicine and Endocrinology. Satoru Noguchi studied Sarcoglycanopathy and Sarcospan that intersect with Cell signaling. His Neuroscience research is multidisciplinary, incorporating elements of MAP1LC3B, Chaperone-mediated autophagy and Autophagy database.
Satoru Noguchi spends much of his time researching Myopathy, Pathology, Muscular dystrophy, Genetics and Internal medicine. Satoru Noguchi has researched Myopathy in several fields, including Rimmed vacuoles, Sialic acid, Hereditary inclusion body myopathy, Vacuole and Muscle atrophy. His Pathology research integrates issues from Emerin and Muscle weakness, Anatomy.
His Muscular dystrophy research incorporates themes from Limb-girdle muscular dystrophy, Duchenne muscular dystrophy, Gene mutation and Muscle disorder. His work focuses on many connections between Internal medicine and other disciplines, such as Endocrinology, that overlap with his field of interest in Endoplasmic reticulum. His work in the fields of Dystrophin, such as Sarcoglycan, overlaps with other areas such as Dystrophin-associated protein.
Satoru Noguchi mostly deals with Muscle weakness, Muscle biopsy, RYR1, Myopathy and Malignant hyperthermia. His studies in Muscle weakness integrate themes in fields like Rimmed vacuoles, Ptosis, Oculopharyngeal muscular dystrophy, Skin biopsy and Hypotonia. His research in Hypotonia intersects with topics in Pathological, Bioinformatics, X-linked myotubular myopathy, Medical genetics and Myotubularin.
His work carried out in the field of Myopathy brings together such families of science as Molecular biology, Chaperone and Missense mutation. His Molecular biology study incorporates themes from Limb-girdle muscular dystrophy, Collagen VI, Huntingtin and Mutation. His work in Skeletal muscle addresses subjects such as Exome sequencing, which are connected to disciplines such as Internal medicine.
Satoru Noguchi mainly focuses on Muscle biopsy, Neurology, Muscular dystrophy, Nonsense and Muscle weakness. His work deals with themes such as Cancer research, Interquartile range, Myositis, Skin biopsy and Huntingtin, which intersect with Muscle biopsy. His Neurology study integrates concerns from other disciplines, such as Dermatology, Dermatomyositis, Rash, Autoantibody and Disease.
His study with Muscular dystrophy involves better knowledge in Genetics. The Nonsense study combines topics in areas such as Sarcolemma, Atrioventricular block, Biceps, Exon and Nonsense mutation. His Muscle weakness research includes elements of Rimmed vacuoles, Immunohistochemistry, Pathology and Ptosis, Oculopharyngeal muscular dystrophy.
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.
Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy
Satoru Noguchi;Elizabeth M. McNally;Kamel Ben Othmane;Yasuko Hagiwara.
From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy
Eijiro Ozawa;Satoru Noguchi;Yuji Mizuno;Yasuko Hagiwara.
Muscle & Nerve (1998)
Dystrophin-associated proteins in muscular dystrophy
Eijiro Ozawa;Mikiharu Yoshida;Atsushi Suzuki;Yuji Mizuno.
Human Molecular Genetics (1995)
Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside.
Mikiharu Yoshida;Atsushi Suzuki;Hideko Yamamoto;Satoru Noguchi.
FEBS Journal (1994)
Selective deficiency of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
Y.K. Hayashi;M. Ogawa;K. Tagawa;S. Noguchi.
Mutations in the sarcoglycan genes in patients with myopathy.
David J. Duggan;J. Rafael Gorospe;Marina Fanin;Eric P. Hoffman.
The New England Journal of Medicine (1997)
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy
Ichizo Nishino;S. Noguchi;K. Murayama;A. Driss.
Autophagic degradation of nuclear components in mammalian cells.
Young-Eun Park;Yukiko K Hayashi;Gisèle Bonne;Takuro Arimura.
Mutations That Disrupt the Carboxyl-Terminus of γ-Sarcoglycan Cause Muscular Dystrophy
Elizabeth M. McNally;David Duggan;J. Rafael Gorospe;Carsten G. Bönnemann.
Human Molecular Genetics (1996)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: