Pages that link to "Q28119088"
Jump to navigation
Jump to search
The following pages link to Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomes (Q28119088):
Displaying 50 items.
- protein tyrosine kinase 2 beta (Q21101275) (← links)
- Nephrocystin 1 (Q21113785) (← links)
- Nephrocystin 4 (Q21118162) (← links)
- Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia (Q24298711) (← links)
- Uromodulin is expressed in renal primary cilia and UMOD mutations result in decreased ciliary uromodulin expression (Q24300384) (← links)
- Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways (Q24302034) (← links)
- Nephrocystins and MKS proteins interact with IFT particle and facilitate transport of selected ciliary cargos (Q24304173) (← links)
- The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome (Q24308784) (← links)
- CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium (Q24310530) (← links)
- Jouberin localizes to collecting ducts and interacts with nephrocystin-1 (Q24314517) (← links)
- Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia (Q24315070) (← links)
- The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4 (Q24336477) (← links)
- Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations (Q24535622) (← links)
- Nephronophthisis (Q24601139) (← links)
- Mechanisms of Nephronophthisis and Related Ciliopathies (Q24634201) (← links)
- CSPP-L Associates with the Desmosome of Polarized Epithelial Cells and Is Required for Normal Spheroid Formation (Q27301019) (← links)
- Nephronophthisis and related syndromes (Q28081939) (← links)
- Multiprotein complexes of Retinitis Pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked Retinitis Pigmentosa (XLRP). (Q28114957) (← links)
- Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6 (Q28116478) (← links)
- The ciliary protein nephrocystin-4 translocates the canonical Wnt regulator Jade-1 to the nucleus to negatively regulate β-catenin signaling (Q28116639) (← links)
- Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization (Q28119115) (← links)
- Casein kinase 1 α phosphorylates the Wnt regulator Jade-1 and modulates its activity (Q28245461) (← links)
- Anks3 interacts with nephronophthisis proteins and is required for normal renal development (Q28578791) (← links)
- Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia (Q28585433) (← links)
- NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development (Q28586324) (← links)
- Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis (Q28586772) (← links)
- Ciliopathies (Q29614821) (← links)
- Genetic Modifiers of Age at Onset in Carriers of the G206A Mutation in PSEN1 With Familial Alzheimer Disease Among Caribbean Hispanics (Q30009136) (← links)
- Joubert syndrome: insights into brain development, cilium biology, and complex disease (Q33580854) (← links)
- Nephronophthisis: disease mechanisms of a ciliopathy (Q33594278) (← links)
- The Ciliary Transition Zone: Finding the Pieces and Assembling the Gate (Q33654636) (← links)
- CSPP is a ciliary protein interacting with Nephrocystin 8 and required for cilia formation (Q34029300) (← links)
- NPHP4 controls ciliary trafficking of membrane proteins and large soluble proteins at the transition zone. (Q34433457) (← links)
- Ciliopathy proteins establish a bipartite signaling compartment in a C. elegans thermosensory neuron (Q34698580) (← links)
- Nephronophthisis. (Q34793373) (← links)
- Ciliary diffusion barrier: the gatekeeper for the primary cilium compartment (Q35126782) (← links)
- Stem cells and fluid flow drive cyst formation in an invertebrate excretory organ (Q35845360) (← links)
- The ciliary transition zone: from morphology and molecules to medicine (Q35902400) (← links)
- Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons (Q36023714) (← links)
- Scoring a backstage pass: mechanisms of ciliogenesis and ciliary access. (Q36027360) (← links)
- Genetic basis of Joubert syndrome and related disorders of cerebellar development (Q36294694) (← links)
- Insights into X-linked retinitis pigmentosa type 3, allied diseases and underlying pathomechanisms (Q36294702) (← links)
- Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease? (Q36337939) (← links)
- Senior-Løken syndrome: a syndromic form of retinal dystrophy associated with nephronophthisis (Q36417359) (← links)
- Cystic kidney diseases: many ways to form a cyst (Q36420786) (← links)
- The Caenorhabditis elegans nephrocystins act as global modifiers of cilium structure (Q36491758) (← links)
- Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease (Q36505469) (← links)
- Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis (Q36631120) (← links)
- Post-translational modifications in the rat lumbar spinal cord in experimental autoimmune encephalomyelitis (Q36731748) (← links)
- Building it up and taking it down: the regulation of vertebrate ciliogenesis (Q37147143) (← links)