Human desmin-coding gene: complete nucleotide sequence, characterization and regulation of expression during myogenesis and development.
about
The toxic effect of R350P mutant desmin in striated muscle of man and mouseA dysfunctional desmin mutation in a patient with severe generalized myopathySevere infantile-onset cardiomyopathy associated with a homozygous deletion in desmin.Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation.Interaction of Theiler's virus with intermediate filaments of infected cellsDesmin-related myopathies in mice and man.Identification and mutational analysis of the glycosylation sites of human keratin 18.Two desmin gene mutations associated with myofibrillar myopathies in Polish familiesCompound heterozygosity of predicted loss-of-function DES variants in a family with recessive desminopathyDesmin splice variants causing cardiac and skeletal myopathy.Assessing self-renewal and differentiation in human embryonic stem cell lines.Desminopathies in muscle disease.Inhibition of desmin expression blocks myoblast fusion and interferes with the myogenic regulators MyoD and myogenin.Desminopathies: pathology and mechanisms.Tragedy in a heartbeat: malfunctioning desmin causes skeletal and cardiac muscle diseaseMolecular pathology of myofibrillar myopathies.Intermediate filament diseases: desminopathy.Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene.Extracellular signal-regulated protein kinase mediates interleukin 17 (IL-17)-induced IL-8 secretion in Helicobacter pylori-infected human gastric epithelial cells.Desmin-related myopathy.A novel site, Mt, in the human desmin enhancer is necessary for maximal expression in skeletal muscle.Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissueStructural and functional analysis of a new desmin variant causing desmin-related myopathy.Intermediate filaments: regulation of gene expression and assembly.An RFLP map for 2q33-q37 from multicase mycobacterial and leishmanial disease families: no evidence for an Lsh/Ity/Bcg gene homologue influencing susceptibility to leprosy.Assembly of amino-terminally deleted desmin in vimentin-free cells.The mouse filensin gene: structure and evolutionary relation to other intermediate filament genes.Lack of desmin results in abortive muscle regeneration and modifications in synaptic structure.Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patients.Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.The identification of myogenic cells in skeletal muscle, with emphasis on the use of tritiated thymidine autoradiography and desmin antibodies.TGF-alpha, EGF, and their cognate EGF receptor are co-expressed with desmin during embryonic, fetal, and neonatal myogenesis in mouse tongue development.Familial cardioneuromyopathy with hyaline masses and nemaline rods: a novel phenotype.Molecular insights into cardiomyopathies associated with desmin (DES) mutations
P2860
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P2860
Human desmin-coding gene: complete nucleotide sequence, characterization and regulation of expression during myogenesis and development.
description
1989 nî lūn-bûn
@nan
1989 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年学术文章
@wuu
1989年学术文章
@zh-cn
1989年学术文章
@zh-hans
1989年学术文章
@zh-my
1989年学术文章
@zh-sg
1989年學術文章
@yue
name
Human desmin-coding gene: comp ...... ng myogenesis and development.
@ast
Human desmin-coding gene: comp ...... ng myogenesis and development.
@en
Human desmin-coding gene: comp ...... ng myogenesis and development.
@nl
type
label
Human desmin-coding gene: comp ...... ng myogenesis and development.
@ast
Human desmin-coding gene: comp ...... ng myogenesis and development.
@en
Human desmin-coding gene: comp ...... ng myogenesis and development.
@nl
prefLabel
Human desmin-coding gene: comp ...... ng myogenesis and development.
@ast
Human desmin-coding gene: comp ...... ng myogenesis and development.
@en
Human desmin-coding gene: comp ...... ng myogenesis and development.
@nl
P2093
P1433
P1476
Human desmin-coding gene: comp ...... ng myogenesis and development.
@en
P2093
Butler-Browne G
Lilienbaum A
P304
P356
10.1016/0378-1119(89)90227-8
P407
P577
1989-05-01T00:00:00Z