Pages that link to "Q28506100"
Jump to navigation
Jump to search
The following pages link to Impaired Wnt-beta-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy (Q28506100):
Displaying 50 items.
- Jouberin (Q21983459) (← links)
- A meckelin-filamin A interaction mediates ciliogenesis (Q24298551) (← links)
- TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone (Q24299114) (← links)
- BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes (Q24301377) (← links)
- Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways (Q24302034) (← links)
- The Joubert syndrome-associated missense mutation (V443D) in the Abelson-helper integration site 1 (AHI1) protein alters its localization and protein-protein interactions (Q24337384) (← links)
- Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome (Q24622660) (← links)
- Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes (Q24625476) (← links)
- Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences (Q24629091) (← links)
- The role of primary cilia in neuronal function (Q24632925) (← links)
- Cilia in autophagy and cancer (Q26768687) (← links)
- Wnt/β-catenin signaling in kidney injury and repair: a double-edged sword (Q26774029) (← links)
- Cilia in vertebrate development and disease (Q26829114) (← links)
- Primary cilia in the developing and mature brain (Q27002324) (← links)
- Scrutinizing ciliopathies by unraveling ciliary interaction networks (Q27025614) (← links)
- CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies (Q27301023) (← links)
- Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome (Q27319191) (← links)
- Mouse models of ciliopathies: the state of the art. (Q27692039) (← links)
- A ciliopathy complex at the transition zone protects the cilia as a privileged membrane domain (Q28000085) (← links)
- Trafficking in and to the primary cilium (Q28000124) (← links)
- The ciliary protein nephrocystin-4 translocates the canonical Wnt regulator Jade-1 to the nucleus to negatively regulate β-catenin signaling (Q28116639) (← links)
- AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis (Q28509528) (← links)
- Neuronal Abelson helper integration site-1 (Ahi1) deficiency in mice alters TrkB signaling with a depressive phenotype. (Q28510053) (← links)
- Neural mechanisms underlying stress resilience in Ahi1 knockout mice: relevance to neuropsychiatric disorders (Q29036263) (← links)
- The primary cilium: a signalling centre during vertebrate development (Q29547197) (← links)
- Preferred SH3 domain partners of ADAM metalloproteases include shared and ADAM-specific SH3 interactions (Q30009199) (← links)
- AHI-1: a novel signaling protein and potential therapeutic target in human leukemia and brain disorders (Q30010179) (← links)
- The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity. (Q30540974) (← links)
- Carcinogens induce loss of the primary cilium in human renal proximal tubular epithelial cells independently of effects on the cell cycle (Q30541981) (← links)
- Lights on for aminopeptidases in cystic kidney disease (Q33685714) (← links)
- Murine Joubert syndrome reveals Hedgehog signaling defects as a potential therapeutic target for nephronophthisis (Q33919616) (← links)
- Primary cilia are required in a unique subpopulation of neural progenitors (Q34119929) (← links)
- Cilia in the CNS: the quiet organelle claims center stage (Q34173153) (← links)
- Ciliopathies: the trafficking connection (Q34207085) (← links)
- Nuclear expression of β-catenin promotes RB stability and resistance to TNF-induced apoptosis in colon cancer cells (Q34314699) (← links)
- Renal-retinal ciliopathy gene Sdccag8 regulates DNA damage response signaling (Q34427583) (← links)
- Cby1 promotes Ahi1 recruitment to a ring-shaped domain at the centriole-cilium interface and facilitates proper cilium formation and function (Q34504028) (← links)
- Kif3a controls murine nephron number via GLI3 repressor, cell survival, and gene expression in a lineage-specific manner (Q34769952) (← links)
- Subcellular spatial regulation of canonical Wnt signalling at the primary cilium (Q35022258) (← links)
- Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome (Q35032831) (← links)
- Cilium, centrosome and cell cycle regulation in polycystic kidney disease. (Q35112926) (← links)
- β-catenin links von Hippel-Lindau to aurora kinase A and loss of primary cilia in renal cell carcinoma (Q35124210) (← links)
- The ciliary proteins Meckelin and Jouberin are required for retinoic acid-dependent neural differentiation of mouse embryonic stem cells (Q35166357) (← links)
- Selective dicer suppression in the kidney alters GSK3β/β-catenin pathways promoting a glomerulocystic disease (Q35208121) (← links)
- Cilia and cell cycle re-entry: more than a coincidence (Q35559947) (← links)
- A Notch-dependent molecular circuitry initiates pancreatic endocrine and ductal cell differentiation (Q36058628) (← links)
- The ciliopathies: a transitional model into systems biology of human genetic disease (Q36433131) (← links)
- LDL Receptor-Related Protein 6 Modulates Ret Proto-Oncogene Signaling in Renal Development and Cystic Dysplasia. (Q36514895) (← links)
- Cilia, Wnt signaling, and the cytoskeleton (Q36564463) (← links)
- Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins (Q36585455) (← links)