A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.

A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.

Item
http://www.wikidata.org/entity/Q41932839
De novo mutations in moderate or severe intellectual disabilityExpansion and concatenation of non-muscle myosin IIA filaments drive cellular contractile system formation during interphase and mitosis.A point mutation in Myh10 causes major defects in heart development and body wall closureThe role of vertebrate nonmuscle Myosin II in development and human disease.Genetic causes of congenital diaphragmatic herniaCytoplasmic mislocalization of RNA splicing factors and aberrant neuronal gene splicing in TDP-43 transgenic pig brain.Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases.Congenital diaphragmatic hernias: from genes to mechanisms to therapies.Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development.
P2860

A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.

Item
http://www.wikidata.org/entity/Q41932839
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.
@en
type
label
A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.
@en
prefLabel
A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P478
P50
P577
P5875
P698
P932
P356
P1433
P1476
A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.
@en
P2093
P2860
P304
P31
P356
P478
P50
P577
P5875
P698
P932