Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
about
Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesiaGenetics and biology of primary ciliary dyskinesiaThe awesome power of dikaryons for studying flagella and basal bodies in Chlamydomonas reinhardtiiCCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic ciliaThe PDZ Protein Na+/H+ Exchanger Regulatory Factor-1 (NHERF1) Regulates Planar Cell Polarity and Motile Cilia OrganizationLRRC6 mutation causes primary ciliary dyskinesia with dynein arm defectsPTEN regulates cilia through Dishevelled.Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromesDisruption of the mouse Jhy gene causes abnormal ciliary microtubule patterning and juvenile hydrocephalusCompound heterozygous alterations in intraflagellar transport protein CLUAP1 in a child with a novel Joubert and oral-facial-digital overlap syndromeClinical profile of recurrent community-acquired pneumonia in children.Stem cells and fluid flow drive cyst formation in an invertebrate excretory organCcdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left-right asymmetry.Primary ciliary dyskinesia and associated sensory ciliopathiesPrimary ciliary dyskinesia-causing mutations in Amish and Mennonite communities.Picking up speed: advances in the genetics of primary ciliary dyskinesia.Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy.Expanding horizons: ciliary proteins reach beyond cilia.The role of cilia in the pathogenesis of cystic kidney disease.Cilia and Ear.Heparin cross-linked collagen sponge scaffolds improve functional regeneration of rat tracheal epithelium.Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling.Primary Ciliary Dyskinesia: An Update on New Diagnostic Modalities and Review of the Literature.Intraflagellar transport 88 (IFT88) is crucial for craniofacial development in mice and is a candidate gene for human cleft lip and palate.Clinical analysis of patients with primary ciliary dyskinesia in mainland China.Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.
P2860
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P2860
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
@ast
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
@en
type
label
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
@ast
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
@en
prefLabel
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
@ast
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
@en
P2860
P1476
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
@en
P2093
Margaret W Leigh
Thomas W Ferkol
P2860
P304
P356
10.1016/J.JPEDS.2011.11.024
P407
P577
2011-12-16T00:00:00Z