Protein folding disease and ATP sensitive potassium channel. 2015

Atsushi Sanbe

UI MeSH Term Description Entries
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D015221 Potassium Channels Cell membrane glycoproteins that are selectively permeable to potassium ions. At least eight major groups of K channels exist and they are made up of dozens of different subunits. Ion Channels, Potassium,Ion Channel, Potassium,Potassium Channel,Potassium Ion Channels,Channel, Potassium,Channel, Potassium Ion,Channels, Potassium,Channels, Potassium Ion,Potassium Ion Channel
D016229 Amyloid beta-Peptides Peptides generated from AMYLOID BETA-PEPTIDES PRECURSOR. An amyloid fibrillar form of these peptides is the major component of amyloid plaques found in individuals with Alzheimer's disease and in aged individuals with trisomy 21 (DOWN SYNDROME). The peptide is found predominantly in the nervous system, but there have been reports of its presence in non-neural tissue. Alzheimer beta-Protein,Amyloid Protein A4,Amyloid beta-Peptide,Amyloid beta-Protein,beta Amyloid,beta-Amyloid Protein,Alzheimer's ABP,Alzheimer's Amyloid Fibril Protein,Amyloid AD-AP,Amyloid Fibril Protein, Alzheimer's,Amyloid beta-Proteins,ABP, Alzheimer's,AD-AP, Amyloid,Alzheimer ABP,Alzheimer beta Protein,Alzheimers ABP,Amyloid AD AP,Amyloid beta Peptide,Amyloid beta Peptides,Amyloid beta Protein,Amyloid beta Proteins,Amyloid, beta,Protein A4, Amyloid,Protein, beta-Amyloid,beta Amyloid Protein,beta-Peptide, Amyloid,beta-Peptides, Amyloid,beta-Protein, Alzheimer,beta-Protein, Amyloid,beta-Proteins, Amyloid
D016923 Cell Death The termination of the cell's ability to carry out vital functions such as metabolism, growth, reproduction, responsiveness, and adaptability. Death, Cell
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus
D057165 Proteostasis Deficiencies Disorders caused by imbalances in the PROTEIN HOMEOSTASIS network - synthesis, folding, and transport of proteins; post-translational modifications; and degradation or clearance of misfolded proteins. Protein Misfolding Disorders,Proteinopathy,Protein Folding Diseases,Protein Folding Disorders,Protein Misfolding Diseases,Proteostasis Dysfunctions,Deficiency, Proteostasis,Disease, Protein Folding,Disease, Protein Misfolding,Disorder, Protein Folding,Disorder, Protein Misfolding,Dysfunction, Proteostasis,Folding Disease, Protein,Folding Disorder, Protein,Misfolding Disease, Protein,Misfolding Disorder, Protein,Protein Folding Disease,Protein Folding Disorder,Protein Misfolding Disease,Protein Misfolding Disorder,Proteinopathies,Proteostasis Deficiency,Proteostasis Dysfunction
D020914 Myopathies, Structural, Congenital A heterogeneous group of diseases characterized by the early onset of hypotonia, developmental delay of motor skills, non-progressive weakness. Each of these disorders is associated with a specific histologic muscle fiber abnormality. Centronuclear Myopathy,Congenital Fiber Type Disproportion,Myopathy, Myotubular,Tubular Aggregate Myopathy,Autosomal Dominant Myotubular Myopathy,Autosomal Recessive Centronuclear Myopathy,CFTDM,Congenital Fiber-Type Disproportion,Congenital Myopathy with Fiber Type Disproportion,Congenital Non-Progressive Myopathies,Congenital Structural Myopathies,Fiber-Type Disproportion Myopathy, Congenital,Myopathy, Centronuclear, 1,Myopathy, Centronuclear, Autosomal Dominant,Myopathy, Congenital, With Fiber-Type Disproportion,Myopathy, Tubular Aggregate,Myotubular Myopathy,Myotubular Myopathy 1,Myotubular Myopathy, Autosomal Dominant,Myotubular Myopathy, X-Linked,Non-Progressive Myopathies, Congenital,Structural Myopathies, Congenital,X-Linked Centronuclear Myopathy,X-Linked Myotubular Myopathy,XLMTM,Aggregate Myopathies, Tubular,Aggregate Myopathy, Tubular,Centronuclear Myopathies,Centronuclear Myopathies, X-Linked,Centronuclear Myopathy, X-Linked,Congenital Fiber-Type Disproportions,Congenital Non Progressive Myopathies,Congenital Non-Progressive Myopathy,Congenital Structural Myopathy,Disproportion, Congenital Fiber-Type,Disproportions, Congenital Fiber-Type,Fiber Type Disproportion Myopathy, Congenital,Fiber-Type Disproportion, Congenital,Fiber-Type Disproportions, Congenital,Myopathies, Centronuclear,Myopathies, Congenital Non-Progressive,Myopathies, Congenital Structural,Myopathies, Myotubular,Myopathies, Tubular Aggregate,Myopathies, X-Linked Centronuclear,Myopathies, X-Linked Myotubular,Myopathy, Centronuclear,Myopathy, Congenital Non-Progressive,Myopathy, Congenital Structural,Myopathy, X-Linked Centronuclear,Myopathy, X-Linked Myotubular,Myotubular Myopathies,Myotubular Myopathies, X-Linked,Myotubular Myopathy, X Linked,Non Progressive Myopathies, Congenital,Non-Progressive Myopathy, Congenital,Structural Myopathy, Congenital,Tubular Aggregate Myopathies,X Linked Centronuclear Myopathy,X Linked Myotubular Myopathy,X-Linked Centronuclear Myopathies,X-Linked Myotubular Myopathies
D038203 alpha-Crystallin B Chain One of the alpha crystallin subunits. In addition to being expressed in the lens (LENS, CRYSTALLINE), alpha-crystallin B chain has been found in a variety of tissues such as HEART; BRAIN; MUSCLE; and KIDNEY. Accumulation of the protein in the brain is associated with NEURODEGENERATIVE DISEASES such as CREUTZFELDT-JAKOB SYNDROME and ALEXANDER DISEASE. Crystallins, alpha B Chain,alpha B-Crystallin,Rosenthal Fiber Component,alpha-Crystallin, B Subunit,B Chain, alpha-Crystallin,B Subunit alpha-Crystallin,alpha B Crystallin,alpha Crystallin B Chain,alpha Crystallin, B Subunit

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