Pages that link to "Q26829114"

The following pages link to Cilia in vertebrate development and disease (Q26829114):

Displaying 50 items.

• An inducible CiliaGFP mouse model for in vivo visualization and analysis of cilia in live tissue. (Q22001107) (← links)
• Mammalian axoneme central pair complex proteins: Broader roles revealed by gene knockout phenotypes (Q26770927) (← links)
• The Evi5 family in cellular physiology and pathology (Q27013381) (← links)
• Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function (Q27309098) (← links)
• Iqcg is essential for sperm flagellum formation in mice (Q27330274) (← links)
• MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone (Q27343217) (← links)
• Mouse models of ciliopathies: the state of the art. (Q27692039) (← links)
• The Role of RPGR and Its Interacting Proteins in Ciliopathies (Q28081883) (← links)
• A simple cell-based assay reveals that diverse neuropsychiatric risk genes converge on primary cilia (Q28484197) (← links)
• SDCCAG8 regulates pericentriolar material recruitment and neuronal migration in the developing cortex (Q28507239) (← links)
• ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis (Q28507428) (← links)
• Arl13b-regulated cilia activities are essential for polarized radial glial scaffold formation (Q28507617) (← links)
• TTC26/DYF13 is an intraflagellar transport protein required for transport of motility-related proteins into flagella (Q28585342) (← links)
• Cluap1 localizes preferentially to the base and tip of cilia and is required for ciliogenesis in the mouse embryo (Q28588539) (← links)
• The Rilp-like proteins Rilpl1 and Rilpl2 regulate ciliary membrane content. (Q28592935) (← links)
• A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi (Q28593154) (← links)
• The MIA complex is a conserved and novel dynein regulator essential for normal ciliary motility (Q30538934) (← links)
• Refining genotype-phenotype correlation in Alström syndrome through study of primary human fibroblasts (Q33906983) (← links)
• CYLD mediates ciliogenesis in multiple organs by deubiquitinating Cep70 and inactivating HDAC6. (Q34452444) (← links)
• Tubulin acetylation: responsible enzymes, biological functions and human diseases (Q34487624) (← links)
• Regulation of Sufu activity by p66β and Mycbp provides new insight into vertebrate Hedgehog signaling (Q34518987) (← links)
• Identification and characterization of a novel allele of Caenorhabditis elegans bbs-7. (Q34653584) (← links)
• Function and regulation of primary cilia and intraflagellar transport proteins in the skeleton (Q35101099) (← links)
• BBS4 is necessary for ciliary localization of TrkB receptor and activation by BDNF. (Q35175053) (← links)
• Dido mutations trigger perinatal death and generate brain abnormalities and behavioral alterations in surviving adult mice (Q35485464) (← links)
• Developmental disruptions underlying brain abnormalities in ciliopathies (Q35709972) (← links)
• Observation of the Ciliary Movement of Choroid Plexus Epithelial Cells Ex Vivo. (Q35745826) (← links)
• Katanin p80 regulates human cortical development by limiting centriole and cilia number (Q35797268) (← links)
• Deacetylation of α-tubulin and cortactin is required for HDAC6 to trigger ciliary disassembly. (Q35922131) (← links)
• A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology (Q36060885) (← links)
• Formation of the transition zone by Mks5/Rpgrip1L establishes a ciliary zone of exclusion (CIZE) that compartmentalises ciliary signalling proteins and controls PIP2 ciliary abundance (Q36172263) (← links)
• Regulation of polycystin-1 ciliary trafficking by motifs at its C-terminus and polycystin-2 but not by cleavage at the GPS site (Q36462325) (← links)
• RC/BTB2 is essential for formation of primary cilia in mammalian cells (Q36593829) (← links)
• The continuing challenge of understanding, preventing, and treating neural tube defects. (Q36914843) (← links)
• PACRG, a protein linked to ciliary motility, mediates cellular signaling (Q37052753) (← links)
• Molecular connections between nuclear and ciliary import processes (Q37152626) (← links)
• The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery (Q37161998) (← links)
• Functional interplay between cylindromatosis and histone deacetylase 6 in ciliary homeostasis revealed by phenotypic analysis of double knockout mice. (Q37317317) (← links)
• The Chlamydomonas mutant pf27 reveals novel features of ciliary radial spoke assembly. (Q37601756) (← links)
• Protein quality control by Rer1p in the early secretory pathway: from mechanism to implication in Alzheimer's disease (Q37689657) (← links)
• Centriole splitting caused by loss of the centrosomal linker protein C-NAP1 reduces centriolar satellite density and impedes centrosome amplification. (Q37699012) (← links)
• Compartmentalization of signaling by vesicular trafficking: a shared building design for the immune synapse and the primary cilium (Q38070788) (← links)
• The primary cilium: guardian of organ development and homeostasis (Q38205342) (← links)
• Symmetry breakage in the vertebrate embryo: when does it happen and how does it work? (Q38223849) (← links)
• Progenitor genealogy in the developing cerebral cortex (Q38241685) (← links)
• Beta cell connectivity in pancreatic islets: a type 2 diabetes target? (Q38260861) (← links)
• Metabolic regulation and energy homeostasis through the primary Cilium (Q38301656) (← links)
• Control of Adult Neurogenesis by Short-Range Morphogenic-Signaling Molecules (Q38659223) (← links)
• Phosphorylation-dependent Akt-Inversin interaction at the basal body of primary cilia. (Q38768808) (← links)
• INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (Q38811329) (← links)