Pages that link to "Q24301924"

The following pages link to CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium (Q24301924):

Displaying 50 items.

• Joubert syndrome (Q1101694) (← links)
• Centrosomal protein 41 (Q21114143) (← links)
• Tubulin tyrosine ligase like 6 (Q21135838) (← links)
• Centrosomal protein 41 (Q21494148) (← links)
• C2orf62 and TTC17 are involved in actin organization and ciliogenesis in zebrafish and human (Q24324242) (← links)
• Multivalent Microtubule Recognition by Tubulin Tyrosine Ligase-like Family Glutamylases (Q24337446) (← links)
• The chemical complexity of cellular microtubules: tubulin post-translational modification enzymes and their roles in tuning microtubule functions (Q24633494) (← links)
• Zebrafish: a vertebrate tool for studying basal body biogenesis, structure, and function (Q26750633) (← links)
• Inositol polyphosphate 5-phosphatases; new players in the regulation of cilia and ciliopathies (Q27012842) (← links)
• Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome (Q27319191) (← links)
• The IN/OUT assay: a new tool to study ciliogenesis (Q27320521) (← links)
• KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome (Q27336381) (← links)
• Mouse models of ciliopathies: the state of the art. (Q27692039) (← links)
• The Cilium: Cellular Antenna and Central Processing Unit (Q28075519) (← links)
• Graded Control of Microtubule Severing by Tubulin Glutamylation (Q28116771) (← links)
• Septins: the fourth component of the cytoskeleton (Q28259172) (← links)
• Inhibition of autophagy suppresses sertraline-mediated primary ciliogenesis in retinal pigment epithelium cells (Q28543400) (← links)
• Intestinal cell kinase, a protein associated with endocrine-cerebro-osteodysplasia syndrome, is a key regulator of cilia length and Hedgehog signaling (Q28587273) (← links)
• Vestibular dysfunction, altered macular structure and trait localization in A/J inbred mice (Q30387287) (← links)
• Cytoplasmic carboxypeptidase 5 regulates tubulin glutamylation and zebrafish cilia formation and function (Q33747094) (← links)
• Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population (Q34031174) (← links)
• Ciliopathies: the trafficking connection (Q34207085) (← links)
• Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy (Q34393598) (← links)
• The nphp-2 and arl-13 genetic modules interact to regulate ciliogenesis and ciliary microtubule patterning in C. elegans (Q34679993) (← links)
• The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function (Q34708502) (← links)
• Tubulin glycylases are required for primary cilia, control of cell proliferation and tumor development in colon. (Q34806540) (← links)
• Mechanisms of otoconia and otolith development (Q35788255) (← links)
• Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies (Q35870349) (← links)
• The ciliary transition zone: from morphology and molecules to medicine (Q35902400) (← links)
• A homozygous AHI1 gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: a case report (Q36255442) (← links)
• Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy (Q36277070) (← links)
• Joubert Syndrome in French Canadians and Identification of Mutations in CEP104 (Q36339758) (← links)
• Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome (Q36342477) (← links)
• The ciliopathies: a transitional model into systems biology of human genetic disease (Q36433131) (← links)
• Arl13b and the exocyst interact synergistically in ciliogenesis (Q36463347) (← links)
• Joubert syndrome: genotyping a Northern European patient cohort (Q36475039) (← links)
• Septin cooperation with tubulin polyglutamylation contributes to cancer cell adaptation to taxanes (Q36546567) (← links)
• Mutation spectrum of Joubert syndrome and related disorders among Arabs (Q36671126) (← links)
• Current insights into renal ciliopathies: what can genetics teach us? (Q36780455) (← links)
• Genome-wide screen identifies novel machineries required for both ciliogenesis and cell cycle arrest upon serum starvation (Q36950722) (← links)
• Loss of RPGR glutamylation underlies the pathogenic mechanism of retinal dystrophy caused by TTLL5 mutations (Q36957262) (← links)
• Digenic inheritance in medical genetics (Q37185089) (← links)
• Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders (Q37185993) (← links)
• Primary cilia and kidney injury: current research status and future perspectives (Q37234721) (← links)
• Joubert syndrome: congenital cerebellar ataxia with the molar tooth (Q37257283) (← links)
• Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity (Q37370853) (← links)
• A conserved flagella-associated protein in Chlamydomonas, FAP234, is essential for axonemal localization of tubulin polyglutamylase TTLL9. (Q37416482) (← links)
• RFX7 is required for the formation of cilia in the neural tube (Q37686145) (← links)
• Zebrafish models in cardiac development and congenital heart birth defects (Q38019209) (← links)
• Diffusion tensor imaging and fiber tractography in brain malformations (Q38071553) (← links)