Osteopontin and skeletal muscle myoblasts: association with muscle regeneration and regulation of myoblast function in vitro
about
SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophyOsteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-betaDifferential Gene Expression Profiling of Dystrophic Dog Muscle after MuStem Cell TransplantationModifier genes and their effect on Duchenne muscular dystrophyExpression of osteopontin in patients with thyroid dysfunctionThe mdx mouse model as a surrogate for Duchenne muscular dystrophySex-Specific Muscular Maturation Responses Following Prenatal Exposure to Methylation-Related Micronutrients in PigsPotent pro-inflammatory and pro-fibrotic molecules, osteopontin and galectin-3, are not major disease modulators of laminin α2 chain-deficient muscular dystrophy.Dual effect of a single nucleotide polymorphism in the first intron of the porcine secreted phosphoprotein 1 gene: allele-specific binding of C/EBP beta and activation of aberrant splicing.Osteopontin, inflammation and myogenesis: influencing regeneration, fibrosis and size of skeletal muscleThe effects of MyD88 deficiency on disease phenotype in dysferlin-deficient A/J mice: role of endogenous TLR ligands.Enhanced growth and osteogenic differentiation of human osteoblast-like cells on boron-doped nanocrystalline diamond thin filmsTGFBR2 but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscleCharacterization of hTERT-immortalized osteoblast cell lines generated from wild-type and connexin43-null mouse calvaria.Identification and validation of novel contraction-regulated myokines released from primary human skeletal muscle cellsGenetic Modifiers for Neuromuscular DiseasesRole of TGF-β signaling in inherited and acquired myopathies.Persistently elevated osteopontin serum levels predict mortality in critically ill patients.Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.Expression of Osteopontin in Oral Squamous Cell Carcinoma and its Surgical Margins-An Immunohistochemical Study.The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype: Transcriptome Comparative Analysis Searching for the Protective FactorsImportance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophyAge dependent increase in the levels of osteopontin inhibits skeletal muscle regeneration.Osteopontin deficiency delays inflammatory infiltration and the onset of muscle regeneration in a mouse model of muscle injuryAlterations in osteopontin modify muscle size in females in both humans and mice.DNA Demethylation Rescues the Impaired Osteogenic Differentiation Ability of Human Periodontal Ligament Stem Cells in High Glucose.Myostatin genetic inactivation inhibits myogenesis by muscle-derived stem cells in vitro but not when implanted in the mdx mouse muscle.Osteopontin genetic variants are associated with overall survival in advanced non-small-cell lung cancer patients and bone metastasis.Progressive impairment of muscle regeneration in muscleblind-like 3 isoform knockout mice.OPN-a induces muscle inflammation by increasing recruitment and activation of pro-inflammatory macrophages.Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy.Bone sialoprotein and osteopontin in bone metastasis of osteotropic cancersStructure and function of the skeletal muscle extracellular matrix.The paradox of muscle hypertrophy in muscular dystrophy.Immune-mediated pathology in Duchenne muscular dystrophy.Methods of probing the interactions between small molecules and disordered proteins.Phosphatidylserine directly and positively regulates fusion of myoblasts into myotubes.Outside in: The matrix as a modifier of muscular dystrophy.High molecular weight gingipains from Porphyromonas gingivalis induce cytokine responses from human macrophage-like cells via a nonproteolytic mechanism.Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy.
P2860
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P2860
Osteopontin and skeletal muscle myoblasts: association with muscle regeneration and regulation of myoblast function in vitro
description
2008 nî lūn-bûn
@nan
2008 թուականին հրատարակուած գիտական յօդուած
@hyw
2008 թվականին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@ast
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@en
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@nl
type
label
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@ast
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@en
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@nl
prefLabel
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@ast
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@en
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@nl
P50
P3181
P1476
Osteopontin and skeletal muscl ...... of myoblast function in vitro
@en
P2093
Hyun-Jin Yoo
P304
P3181
P356
10.1016/J.BIOCEL.2008.03.020
P407
P577
2008-01-01T00:00:00Z