LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
about
The molecular basis of emerin-emerin and emerin-BAF interactionsLIMCH1 regulates nonmuscle myosin-II activity and suppresses cell migration.Lmo7 is dispensable for skeletal muscle and cardiac function.Diseases of the Nucleoskeleton.Knockdown of Lmo7 inhibits chick myogenesis.The Pathogenesis and Therapies of Striated Muscle Laminopathies
P2860
LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
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LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
@en
LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
@nl
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label
LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
@en
LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
@nl
prefLabel
LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
@en
LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy.
@nl
P2860
P356
P1433
P1476
LMO7-null mice exhibit phenotypes consistent with emery-dreifuss muscular dystrophy
@en
P2093
Aaron Mull
P2860
P304
P356
10.1002/MUS.24286
P577
2014-11-19T00:00:00Z