Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics.
about
Myofibrillar myopathies: new developments.Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review).RNAi-based gene therapy for dominant Limb Girdle Muscular Dystrophies.Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association oExome analysis of two limb-girdle muscular dystrophy families: mutations identified and challenges encounteredLaser capture microdissection of metachromatically stained skeletal muscle allows quantification of fiber type specific gene expression.Cytosolic 5'-nucleotidase 1A autoimmunity in sporadic inclusion body myositis.Alternative splicing of human insulin receptor gene (INSR) in type I and type II skeletal muscle fibers of patients with myotonic dystrophy type 1 and type 2.A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies.Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies.Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis.Myofibrillar disruption and RNA-binding protein aggregation in a mouse model of limb-girdle muscular dystrophy 1DDesminopathies: pathology and mechanisms.The cell biology of disease: cellular and molecular mechanisms underlying muscular dystrophy.The Classification, Natural History and Treatment of the Limb Girdle Muscular DystrophiesProteomic identification of biomarkers of skeletal muscle disorders.Genetic basis of limb-girdle muscular dystrophies: the 2014 updateCostamere proteins and their involvement in myopathic processes.Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy.DDA: A Novel Network-Based Scoring Method to Identify Disease-Disease Associations.No need for more muscle biopsies in members of the Spanish LGMD1F family. The gene has been identified at last.DNAJB6 myopathy: a vacuolar myopathy with childhood onset.
P2860
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P2860
Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics.
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Etiology of limb girdle muscul ...... re microdissection proteomics.
@ast
Etiology of limb girdle muscul ...... re microdissection proteomics.
@en
Etiology of limb girdle muscul ...... re microdissection proteomics.
@nl
type
label
Etiology of limb girdle muscul ...... re microdissection proteomics.
@ast
Etiology of limb girdle muscul ...... re microdissection proteomics.
@en
Etiology of limb girdle muscul ...... re microdissection proteomics.
@nl
prefLabel
Etiology of limb girdle muscul ...... re microdissection proteomics.
@ast
Etiology of limb girdle muscul ...... re microdissection proteomics.
@en
Etiology of limb girdle muscul ...... re microdissection proteomics.
@nl
P2093
P2860
P356
P1433
P1476
Etiology of limb girdle muscul ...... re microdissection proteomics.
@en
P2093
Daniel P Judge
Hanno Steen
Kathryn R Wagner
Matthew W Feldman
Mohammad Salajegheh
Ralph W Kuncl
Steven A Greenberg
Zachary Waldon
P2860
P304
P356
10.1002/ANA.22649
P577
2012-01-01T00:00:00Z