Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
about
X-linked disorders with cerebellar dysgenesisActive transport of the ubiquitin ligase MID1 along the microtubules is regulated by protein phosphatase 2ALoss of extracellular superoxide dismutase leads to acute lung damage in the presence of ambient air: a potential mechanism underlying adult respiratory distress syndromeHedgehog-dependent E3-ligase Midline1 regulates ubiquitin-mediated proteasomal degradation of Pax6 during visual system development.ISL1 directly regulates FGF10 transcription during human cardiac outflow formation.The Challenge of Prenatal Diagnostic Work-Up of Maternally Inherited X-Linked Opitz G/BBB: Case Report and Literature Review.Alternative polyadenylation signals and promoters act in concert to control tissue-specific expression of the Opitz Syndrome gene MID1.Pediatric primary central nervous system germ cell tumors of different prognosis groups show characteristic miRNome traits and chromosome copy number variations.Mid1/Mid2 expression in craniofacial development and a literature review of X-linked opitz syndrome.Human neural crest cells display molecular and phenotypic hallmarks of stem cellsX-linked Opitz G/BBB syndrome: identification of a novel mutation and prenatal diagnosis in a Korean family.X-linked microtubule-associated protein, Mid1, regulates axon development.Developmental disorders of the midbrain and hindbrain.Molecular mechanisms of cell shape changes that contribute to vertebrate neural tube closure.Cellular and molecular basis of cerebellar development.The multifactorial origin of respiratory morbidity in patients surviving neonatal repair of esophageal atresia.Reduced Mid1 Expression and Delayed Neuromotor Development in daDREAM Transgenic Mice.Dental treatment of a patient with Opitz G/BBB syndrome.Two Novel Pathogenic MID1 Variants and Genotype-Phenotype Correlation Reanalysis in X-Linked Opitz G/BBB Syndrome.A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain.
P2860
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P2860
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
@en
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
@nl
type
label
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
@en
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
@nl
prefLabel
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
@en
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
@nl
P2093
P50
P356
P1476
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome
@en
P2093
M Le Merrer
M Vekemans
P304
P356
10.1136/JMG.2003.014829
P407
P577
2004-05-01T00:00:00Z