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Laminin-Mediated Interactions in Thymocyte Migration and DevelopmentThe potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophyThe laminin response in inflammatory bowel disease: protection or malignancy?Secretome Profiling of Periodontal Ligament from Deciduous and Permanent Teeth Reveals a Distinct Expression Pattern of Laminin ChainsRecent advances using zebrafish animal models for muscle disease drug discoveryPotent pro-inflammatory and pro-fibrotic molecules, osteopontin and galectin-3, are not major disease modulators of laminin α2 chain-deficient muscular dystrophy.Peptide-modified chitosan hydrogels promote skin wound healing by enhancing wound angiogenesis and inhibiting inflammation.Mesenchymal Stromal Cells for Sphincter Regeneration: Role of Laminin Isoforms upon Myogenic Differentiation.Influence of ovarian muscle contraction and oocyte growth on egg chamber elongation in Drosophila.Pathoproteomic profiling of the skeletal muscle matrisome in dystrophinopathy associated myofibrosis.Absence of microRNA-21 does not reduce muscular dystrophy in mouse models of LAMA2-CMDMuscular dystrophy in a dish: engineered human skeletal muscle mimetics for disease modeling and drug discovery.The role of laminins in the organization and function of neuromuscular junctions.G Protein-Coupled Receptors in Myelinating Glia.Promoting differentiation of cultured myoblasts using biomimetic surfaces that present alpha-laminin-2 peptides.Deletion of integrin α7 subunit does not aggravate the phenotype of laminin α2 chain-deficient mice.The evolution of the dystroglycan complex, a major mediator of muscle integrity.Regulation of the blood-testis barrier by a local axis in the testis: role of laminin α2 in the basement membrane.The laminin family: founding members of the basement membrane.Lectin-binding characterizes the healthy human skeletal muscle glycophenotype and identifies disease-specific changes in dystrophic muscle.Peptide-Modified Chitosan Hydrogels Accelerate Skin Wound Healing by Promoting Fibroblast Proliferation, Migration, and Secretion.Are mechanically sensitive regulators involved in the function and (patho)physiology of cerebral palsy-related contractures?A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese patient.Recapitulation of Extracellular LAMININ Environment Maintains Stemness of Satellite Cells In Vitro.Laminin heparin-binding peptides bind to several growth factors and enhance diabetic wound healing.Shaping Synapses by the Neural Extracellular Matrix.
P2860
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P2860
description
2012 nî lūn-bûn
@nan
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
2012年论文
@zh
2012年论文
@zh-cn
name
Laminin-211 in skeletal muscle function.
@ast
Laminin-211 in skeletal muscle function.
@en
type
label
Laminin-211 in skeletal muscle function.
@ast
Laminin-211 in skeletal muscle function.
@en
prefLabel
Laminin-211 in skeletal muscle function.
@ast
Laminin-211 in skeletal muscle function.
@en
P2860
P356
P1476
Laminin-211 in skeletal muscle function.
@en
P2093
Johan Holmberg
Madeleine Durbeej
P2860
P304
P356
10.4161/CAM.22618
P577
2012-11-15T00:00:00Z