about
Axonemal positioning and orientation in three-dimensional space for primary cilia: what is known, what is assumed, and what needs clarificationRer1p maintains ciliary length and signaling by regulating γ-secretase activity and Foxj1a levels.Neural crest cell signaling pathways critical to cranial bone development and pathology.Function and regulation of primary cilia and intraflagellar transport proteins in the skeletonMidline craniofacial malformations with a lipomatous cephalocele are associated with insufficient closure of the neural tube in the tuft mouse.Using the avian mutant talpid2 as a disease model for understanding the oral-facial phenotypes of oral-facial-digital syndromeCraniofacial Ciliopathies Reveal Specific Requirements for GLI Proteins during Development of the Facial Midline.nlz1 is required for cilia formation in zebrafish embryogenesis.A tissue-specific role for intraflagellar transport genes during craniofacial development.Molecular mechanisms of midfacial developmental defects.Utilizing the chicken as an animal model for human craniofacial ciliopathies.Canonical and noncanonical intraflagellar transport regulates craniofacial skeletal development.Understanding Mechanisms of GLI-Mediated Transcription during Craniofacial Development and Disease Using the Ciliopathic Mutant, talpid2.Joubert syndrome and related disorders, prenatal diagnosis with ultrasound and magnetic resonance imaging.Anosmin-1 over-expression increases adult neurogenesis in the subventricular zone and neuroblast migration to the olfactory bulb.Unmasking the ciliopathies: craniofacial defects and the primary cilium.Discovery, Diagnosis, and Etiology of Craniofacial Ciliopathies.Emerging from their burrow: Hedgehog pathway inhibitors for cancer.Cilia-dependent GLI processing in neural crest cells is required for tongue development.Primary cilia modulate balance of canonical and non-canonical Wnt signaling responses in the injured kidney.Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome).Role of the Primary Cilia on the Macula Densa and Thick Ascending Limbs in Regulation of Sodium Excretion and Hemodynamics.Morphological and molecular changes associated with Pitchfork during mouse palate development.Isolation of primary cilia by shear force.Multiple postnatal craniofacial anomalies are characterized by conditional loss of polycystic kidney disease 2 (Pkd2).SHP2-Deficiency in Chondrocytes Deforms Orofacial Cartilage and Ciliogenesis in Mice.Patched1 is required in neural crest cells for the prevention of orofacial clefts.Cilia length and intraflagellar transport regulation by kinases PKG-1 and GCK-2 in C. elegans sensory neurons.BBS9 gene in nonsyndromic craniosynostosis: Role of the primary cilium in the aberrant ossification of the suture osteogenic niche.Hypomorphic Smo mutant with inefficient ciliary enrichment disrupts the highest level of vertebrate Hedgehog response.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
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
name
The emerging face of primary cilia.
@ast
The emerging face of primary cilia.
@en
type
label
The emerging face of primary cilia.
@ast
The emerging face of primary cilia.
@en
prefLabel
The emerging face of primary cilia.
@ast
The emerging face of primary cilia.
@en
P2860
P356
P1433
P1476
The emerging face of primary cilia.
@en
P2093
Norann A Zaghloul
Samantha A Brugmann
P2860
P304
P356
10.1002/DVG.20728
P577
2011-04-01T00:00:00Z