Pages that link to "Q39012190"
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The following pages link to Motile and non-motile cilia in human pathology: from function to phenotypes (Q39012190):
Displaying 50 items.
- The Ciliary Transition Zone: Finding the Pieces and Assembling the Gate (Q33654636) (← links)
- Primary Ciliary Dyskinesia: An Update on Clinical Aspects, Genetics, Diagnosis, and Future Treatment Strategies (Q33780616) (← links)
- Toolbox in a tadpole: Xenopus for kidney research (Q38731540) (← links)
- Genetics meets pathology - an increasingly important relationship (Q39012198) (← links)
- The electric fence to cell-cycle progression: Do local changes in membrane potential facilitate disassembly of the primary cilium?: Timely and localized expression of a potassium channel may set the conditions that allow retraction of the primary ci (Q39215812) (← links)
- Oral and Craniofacial Anomalies of Bardet-Biedl Syndrome: Dental Management in the Context of a Rare Disease (Q39405146) (← links)
- The connections of Wnt pathway components with cell cycle and centrosome: side effects or a hidden logic? (Q39457168) (← links)
- Bardet-Biedl Syndrome as a Chaperonopathy: Dissecting the Major Role of Chaperonin-Like BBS Proteins (BBS6-BBS10-BBS12). (Q41170062) (← links)
- Motile cilia defects in diseases other than primary ciliary dyskinesia: The contemporary diagnostic and research role for transmission electron microscopy (Q41596398) (← links)
- The N-terminus of IFT46 mediates intraflagellar transport of outer arm dynein and its cargo-adaptor ODA16. (Q43491669) (← links)
- Hypomorphic Recessive Variants in SUFU Impair the Sonic Hedgehog Pathway and Cause Joubert Syndrome with Cranio-facial and Skeletal Defects. (Q46233034) (← links)
- DRC2/CCDC65 is a central hub for assembly of the nexin-dynein regulatory complex and other regulators of ciliary and flagellar motility (Q46255742) (← links)
- Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies (Q46904962) (← links)
- Primary cilia proteins: ciliary and extraciliary sites and functions. (Q47228439) (← links)
- Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathies. (Q47625348) (← links)
- The formation of the light-sensing compartment of cone photoreceptors coincides with a transcriptional switch. (Q47652965) (← links)
- Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome. (Q47757055) (← links)
- Phenotypes, pleiotropy, and phylogeny. (Q48188504) (← links)
- WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome (Q48374383) (← links)
- Kidney-differentiated cells derived from Lowe Syndrome patient's iPSCs show ciliogenesis defects and Six2 retention at the Golgi complex (Q50000144) (← links)
- Drosophila PLP assembles pericentriolar clouds that promote centriole stability, cohesion and MT nucleation (Q50099523) (← links)
- Managing Bardet–Biedl Syndrome—Now and in the Future (Q50301044) (← links)
- C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia (Q54850008) (← links)
- Disease-Associated Mutations in CEP120 Destabilize the Protein and Impair Ciliogenesis. (Q55003855) (← links)
- Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes. (Q55380590) (← links)
- Primary cilium and glioblastoma (Q57298233) (← links)
- Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome (Q58608214) (← links)
- Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects (Q58618792) (← links)
- Tailoring Formulations for Intranasal Nose-to-Brain Delivery: A Review on Architecture, Physico-Chemical Characteristics and Mucociliary Clearance of the Nasal Olfactory Mucosa (Q58800789) (← links)
- Proteomic Profiles in Advanced Age-Related Macular Degeneration Using an Aptamer-Based Proteomic Technology (Q61443825) (← links)
- A liquid-like organelle at the root of motile ciliopathy (Q61444117) (← links)
- Ciliary Beating Compartmentalizes Cerebrospinal Fluid Flow in the Brain and Regulates Ventricular Development (Q61445964) (← links)
- Survey of the Ciliary Motility Machinery of Sperm and Ciliated Mechanosensory Neurons Reveals Unexpected Cell-Type Specific Variations: A Model for Motile Ciliopathies (Q61803764) (← links)
- Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project (Q64039678) (← links)
- Adolescent idiopathic scoliosis associated POC5 mutation impairs cell cycle, cilia length and centrosome protein interactions (Q64123337) (← links)
- Microscopy-Based Automated Live Cell Screening for Small Molecules That Affect Ciliation (Q64252069) (← links)
- Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus. (Q64914313) (← links)
- Asymmetric distribution and spatial switching of dynein activity generates ciliary motility (Q88487954) (← links)
- Macular staphyloma in patients affected by Joubert syndrome with retinal dystrophy: a new finding detected by SD-OCT (Q89483902) (← links)
- The "salt and pepper" pattern on renal ultrasound in a group of children with molecular-proven diagnosis of ciliopathy-related renal diseases (Q89629635) (← links)
- Phosphorylation of multiple proteins involved in ciliogenesis by Tau Tubulin kinase 2 (Q90028602) (← links)
- MKS-NPHP module proteins control ciliary shedding at the transition zone (Q90262455) (← links)
- NPHP proteins are binding partners of nucleoporins at the base of the primary cilium (Q90280361) (← links)
- The ciliary protein Rpgrip1l in development and disease (Q90740314) (← links)
- Altered generation of ciliated cells in chronic obstructive pulmonary disease (Q91559850) (← links)
- Role of the Novel Hsp90 Co-Chaperones in Dynein Arms' Preassembly (Q91815903) (← links)
- Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis (Q92068053) (← links)
- Wnt-PLC-IP3-Connexin-Ca2+ axis maintains ependymal motile cilia in zebrafish spinal cord (Q92092559) (← links)
- A nanostructure platform for live-cell manipulation of membrane curvature (Q92126192) (← links)
- Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes (Q92328862) (← links)