Laminin-α2 Chain-Deficient Congenital Muscular Dystrophy: Pathophysiology and Development of Treatment.
about
A novel early onset phenotype in a zebrafish model of merosin deficient congenital muscular dystrophyLaminin: loss-of-function studies.Adhesion G-protein coupled receptors and extracellular matrix proteins: Roles in myelination and glial cell development.Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism.Bioenergetic Impairment in Congenital Muscular Dystrophy Type 1A and Leigh Syndrome Muscle CellsEngineering micromyocardium to delineate cellular and extracellular regulation of myocardial tissue contractility.Aberrant Caspase Activation in Laminin-α2-Deficient Human Myogenic Cells is Mediated by p53 and Sirtuin Activity.Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy.Muscular dystrophy meets protein biochemistry, the mother of invention.Natural disease history of the dy2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy.Effects of metformin on congenital muscular dystrophy type 1A disease progression in mice: a gender impact study
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P2860
Laminin-α2 Chain-Deficient Congenital Muscular Dystrophy: Pathophysiology and Development of Treatment.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
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2015年學術文章
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2015年學術文章
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name
Laminin-α2 Chain-Deficient Con ...... and Development of Treatment.
@en
type
label
Laminin-α2 Chain-Deficient Con ...... and Development of Treatment.
@en
prefLabel
Laminin-α2 Chain-Deficient Con ...... and Development of Treatment.
@en
P1476
Laminin-α2 Chain-Deficient Con ...... and Development of Treatment.
@en
P2093
Madeleine Durbeej
P356
10.1016/BS.CTM.2015.05.002
P577
2015-01-01T00:00:00Z