Pages that link to "Q34341740"
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The following pages link to Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice. (Q34341740):
Displaying 50 items.
- A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence (Q21092494) (← links)
- Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function (Q21145277) (← links)
- The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein (Q24292750) (← links)
- The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly (Q24293516) (← links)
- Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy (Q24299464) (← links)
- BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes (Q24301377) (← links)
- Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis (Q24310102) (← links)
- Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia (Q24315070) (← links)
- The Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formation (Q24316483) (← links)
- Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport (Q24564553) (← links)
- Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia (Q24633410) (← links)
- Mutations in a NIMA-related kinase gene, Nek1, cause pleiotropic effects including a progressive polycystic kidney disease in mice (Q24648390) (← links)
- Cilia/Ift protein and motor -related bone diseases and mouse models (Q26865112) (← links)
- Pathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapy (Q27000075) (← links)
- A Cilia Independent Role of Ift88/Polaris during Cell Migration (Q27313531) (← links)
- The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes (Q27342580) (← links)
- The intraflagellar transport machinery of Chlamydomonas reinhardtii (Q27919639) (← links)
- Trafficking to the ciliary membrane: how to get across the periciliary diffusion barrier? (Q27967655) (← links)
- Architecture and function of IFT complex proteins in ciliogenesis (Q28000079) (← links)
- Intraflagellar transport (Q28131775) (← links)
- IFT20 links kinesin II with a mammalian intraflagellar transport complex that is conserved in motile flagella and sensory cilia (Q28181491) (← links)
- Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination (Q28188363) (← links)
- Biochemical and molecular characterization of diseases linked to motor proteins (Q28209818) (← links)
- Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells (Q28505110) (← links)
- The primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiation (Q28507794) (← links)
- ADP-ribosylation factor-like 3 is involved in kidney and photoreceptor development (Q28512728) (← links)
- Phenotypic variations of orpk mutation and chromosomal localization of modifiers influencing kidney phenotype (Q28512820) (← links)
- Hedgehog signaling and primary cilia are required for the formation of adult neural stem cells (Q28512856) (← links)
- Nek8 regulates the expression and localization of polycystin-1 and polycystin-2 (Q28513278) (← links)
- Primary cilia dynamics instruct tissue patterning and repair of corneal endothelium (Q28513509) (← links)
- Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease (Q28585961) (← links)
- Primary cilia regulate Shh activity in the control of molar tooth number (Q28586953) (← links)
- Loss of the Tg737 protein results in skeletal patterning defects (Q28588662) (← links)
- Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesion (Q28591525) (← links)
- Knockdown of the intraflagellar transport protein IFT46 stimulates selective gene expression in mouse chondrocytes and affects early development in zebrafish (Q28592778) (← links)
- Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease (Q28592889) (← links)
- Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella (Q28593253) (← links)
- IFT80 is essential for chondrocyte differentiation by regulating Hedgehog and Wnt signaling pathways (Q28593506) (← links)
- Endothelial cilia are fluid shear sensors that regulate calcium signaling and nitric oxide production through polycystin-1 (Q28593836) (← links)
- A mutation in the mouse ttc26 gene leads to impaired hedgehog signaling (Q28863488) (← links)
- An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons (Q28611301) (← links)
- Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms (Q29614613) (← links)
- The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance (Q29620386) (← links)
- Dicer regulates the development of nephrogenic and ureteric compartments in the mammalian kidney (Q30429774) (← links)
- Function and dynamics of PKD2 in Chlamydomonas reinhardtii flagella (Q30441836) (← links)
- From central to rudimentary to primary: the history of an underappreciated organelle whose time has come. The primary cilium (Q30450537) (← links)
- XBX-1 encodes a dynein light intermediate chain required for retrograde intraflagellar transport and cilia assembly in Caenorhabditis elegans (Q30478329) (← links)
- Cftr controls lumen expansion and function of Kupffer's vesicle in zebrafish (Q30538611) (← links)
- Situs inversus and ciliary abnormalities: 20 years later, what is the connection? (Q30615165) (← links)
- Utilization of microhomologous recombination in yeast to generate targeting constructs for mammalian genes (Q32060172) (← links)