In vivo characterization of human myofibrillar myopathy genes in zebrafish.
about
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism.Atrogin-1 Deficiency Leads to Myopathy and Heart Failure in Zebrafish.A compact unc45b-promoter drives muscle-specific expression in zebrafish and mouse.215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13-15 November 2015, Heemskerk, The Netherlands.CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency.How the expression of green fluorescent protein and human cardiac actin in the heart influences cardiac function and aerobic performance in zebrafish Danio rerio.Loss of αB-crystallin function in zebrafish reveals critical roles in the development of the lens and stress resistance of the heart.Genetics of Cardiovascular Disease: Fishing for Causality.Loss of the novel Vcp (valosin containing protein) interactor Washc4 interferes with autophagy-mediated proteostasis in striated muscle and leads to myopathy in vivo
P2860
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P2860
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
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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name
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
@en
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
@nl
type
label
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
@en
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
@nl
prefLabel
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
@en
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
@nl
P2093
P50
P1476
In vivo characterization of human myofibrillar myopathy genes in zebrafish.
@en
P2093
Christoph S Clemen
Dieter O Fürst
Gerhard Wiche
Joachim Schessl
John B Bührdel
Linda Manta
Mirjam Kessler
Monika Forster
Rolf Schröder
Sofia Hirth
P304
P356
10.1016/J.BBRC.2015.03.149
P407
P577
2015-04-09T00:00:00Z