Pages that link to "Q27967648"
Jump to navigation
Jump to search
The following pages link to The nonmotile ciliopathies (Q27967648):
Displaying 50 items.
- Discovering regulators of centriole biogenesis through siRNA-based functional genomics in human cells (Q24295076) (← links)
- Cep126 is required for pericentriolar satellite localisation to the centrosome and for primary cilium formation (Q24298370) (← links)
- Evolutionarily assembled cis-regulatory module at a human ciliopathy locus (Q24303601) (← links)
- Ciliary entry of the kinesin-2 motor KIF17 is regulated by importin-beta2 and RanGTP (Q24621121) (← links)
- The role of primary cilia in neuronal function (Q24632925) (← links)
- Bardet-Biedl Syndrome (Q26744178) (← links)
- Gorab Is Required for Dermal Condensate Cells to Respond to Hedgehog Signals during Hair Follicle Morphogenesis (Q26766281) (← links)
- From quantitative protein complex analysis to disease mechanism (Q26823230) (← links)
- Polycystin-1 cleavage and the regulation of transcriptional pathways (Q27012570) (← links)
- Spectrum of clinical diseases caused by disorders of primary cilia (Q27024881) (← links)
- Scrutinizing ciliopathies by unraveling ciliary interaction networks (Q27025614) (← links)
- Basal body multipotency and axonemal remodelling are two pathways to a 9+0 flagellum. (Q27317104) (← links)
- Pitchfork and Gprasp2 Target Smoothened to the Primary Cilium for Hedgehog Pathway Activation (Q27321217) (← links)
- Mutations in a guanylate cyclase GCY-35/GCY-36 modify Bardet-Biedl syndrome-associated phenotypes in Caenorhabditis elegans (Q27335893) (← links)
- Trafficking to the ciliary membrane: how to get across the periciliary diffusion barrier? (Q27967655) (← links)
- A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition (Q28000057) (← links)
- Trafficking in and to the primary cilium (Q28000124) (← links)
- The axoneme: the propulsive engine of spermatozoa and cilia and associated ciliopathies leading to infertility (Q28066065) (← links)
- Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management (Q28071634) (← links)
- Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa (Q28115096) (← links)
- Transcriptional program of ciliated epithelial cells reveals new cilium and centrosome components and links to human disease (Q28118826) (← links)
- Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization (Q28119115) (← links)
- TTC26/DYF13 is an intraflagellar transport protein required for transport of motility-related proteins into flagella (Q28585342) (← links)
- A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi (Q28593154) (← links)
- The primary cilium: a signalling centre during vertebrate development (Q29547197) (← links)
- From central to rudimentary to primary: the history of an underappreciated organelle whose time has come. The primary cilium (Q30450537) (← links)
- RFX2 is essential in the ciliated organ of asymmetry and an RFX2 transgene identifies a population of ciliated cells sufficient for fluid flow (Q30513992) (← links)
- Protein arginine methyltransferases interact with intraflagellar transport particles and change location during flagellar growth and resorption (Q33632424) (← links)
- Lights on for aminopeptidases in cystic kidney disease (Q33685714) (← links)
- Small organelle, big responsibility: the role of centrosomes in development and disease (Q33959953) (← links)
- The ciliogenic transcription factor RFX3 regulates early midline distribution of guidepost neurons required for corpus callosum development (Q34221020) (← links)
- Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT) (Q34699805) (← links)
- B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis (Q35030818) (← links)
- Regulation of ciliary motility: conserved protein kinases and phosphatases are targeted and anchored in the ciliary axoneme (Q35043160) (← links)
- A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies (Q35063169) (← links)
- Assessing the pathogenic potential of human Nephronophthisis disease-associated NPHP-4 missense mutations in C. elegans (Q35090086) (← links)
- The ciliopathy gene Rpgrip1l is essential for hair follicle development (Q35122197) (← links)
- The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking (Q35225255) (← links)
- Molecular determinants of ciliary membrane localization of Trypanosoma cruzi flagellar calcium-binding protein (Q35312453) (← links)
- Reversible association of tetraspanin with Trichomonas vaginalis flagella upon adherence to host cells (Q35623941) (← links)
- Identification of G Protein-Coupled Receptors (GPCRs) in Primary Cilia and Their Possible Involvement in Body Weight Control (Q35656487) (← links)
- Ciliopathies: the central role of cilia in a spectrum of pediatric disorders (Q35764547) (← links)
- Current understanding of usher syndrome type II. (Q35830124) (← links)
- Protein composition and movements of membrane swellings associated with primary cilia (Q35854986) (← links)
- Structural Characterization of Bardet-Biedl Syndrome 9 Protein (BBS9). (Q35925806) (← links)
- POC1A truncation mutation causes a ciliopathy in humans characterized by primordial dwarfism (Q36152933) (← links)
- Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association (Q36275704) (← links)
- Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome (Q36342477) (← links)
- Coevolution reveals a network of human proteins originating with multicellularity (Q36543191) (← links)
- The kinesin superfamily protein KIF17: one protein with many functions (Q36916585) (← links)