Pages that link to "Q35145360"
Jump to navigation
Jump to search
The following pages link to Altered trafficking and stability of polycystins underlie polycystic kidney disease (Q35145360):
Displaying 50 items.
- Ciliary Extracellular Vesicles: Txt Msg Organelles (Q26764992) (← links)
- The Role of G-Protein-Coupled Receptor Proteolysis Site Cleavage of Polycystin-1 in Renal Physiology and Polycystic Kidney Disease (Q26775090) (← links)
- Role of the Polycystins in Cell Migration, Polarity, and Tissue Morphogenesis (Q26777057) (← links)
- A polycystin-centric view of cyst formation and disease: the polycystins revisited (Q26800974) (← links)
- Model Organisms in G Protein-Coupled Receptor Research (Q28080425) (← links)
- Function and regulation of TRPP2 ion channel revealed by a gain-of-function mutant (Q29147455) (← links)
- Trafficking to the primary cilium membrane. (Q30353488) (← links)
- Autosomal dominant polycystic kidney disease: the changing face of clinical management (Q34481426) (← links)
- Sec63 and Xbp1 regulate IRE1α activity and polycystic disease severity (Q35719978) (← links)
- Myristoylated CIL-7 regulates ciliary extracellular vesicle biogenesis (Q36063776) (← links)
- Human polycystin-2 transgene dose-dependently rescues ADPKD phenotypes in Pkd2 mutant mice (Q36167611) (← links)
- Cell-Specific Transcriptional Profiling of Ciliated Sensory Neurons Reveals Regulators of Behavior and Extracellular Vesicle Biogenesis (Q36422275) (← links)
- An age of enlightenment for cilia: The FASEB summer research conference on the "Biology of Cilia and Flagella" (Q36495042) (← links)
- mTORC1-mediated inhibition of polycystin-1 expression drives renal cyst formation in tuberous sclerosis complex (Q36651027) (← links)
- The Polycystin-1, Lipoxygenase, and α-Toxin Domain Regulates Polycystin-1 Trafficking. (Q36746031) (← links)
- Fatty Acid Oxidation is Impaired in An Orthologous Mouse Model of Autosomal Dominant Polycystic Kidney Disease (Q36753925) (← links)
- Heterotrimeric G protein signaling in polycystic kidney disease (Q37139683) (← links)
- Progress in ciliary ion channel physiology (Q37565663) (← links)
- MAPK-15 is a ciliary protein required for PKD-2 localization and male mating behavior in Caenorhabditis elegans (Q38660692) (← links)
- Isolated polycystic liver disease genes define effectors of polycystin-1 function (Q38708994) (← links)
- Tubby family proteins are adapters for ciliary trafficking of integral membrane proteins (Q38718216) (← links)
- Role of apoptosis in the development of autosomal dominant polycystic kidney disease (ADPKD). (Q38754935) (← links)
- PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis (Q38868452) (← links)
- Predicted Mutation Strength of Nontruncating PKD1 Mutations Aids Genotype-Phenotype Correlations in Autosomal Dominant Polycystic Kidney Disease (Q38914739) (← links)
- Extracellular Loops Are Essential for the Assembly and Function of Polycystin Receptor-Ion Channel Complexes (Q38983072) (← links)
- Primary Cilia in Cystic Kidney Disease (Q39242476) (← links)
- The serologically defined colon cancer antigen-3 (SDCCAG3) is involved in the regulation of ciliogenesis (Q39263072) (← links)
- Molecular diagnosis of autosomal dominant polycystic kidney disease (Q39445724) (← links)
- Phosphoinositide 3-Kinase-C2α Regulates Polycystin-2 Ciliary Entry and Protects against Kidney Cyst Formation (Q39693435) (← links)
- Rapamycin treatment dose-dependently improves the cystic kidney in a new ADPKD mouse model via the mTORC1 and cell-cycle-associated CDK1/cyclin axis. (Q41247634) (← links)
- Structure of the polycystic kidney disease TRP channel Polycystin-2 (PC2). (Q41988618) (← links)
- Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases (Q47781166) (← links)
- Organoid cystogenesis reveals a critical role of microenvironment in human polycystic kidney disease. (Q48260423) (← links)
- A cleavage product of Polycystin-1 is a mitochondrial matrix protein that affects mitochondria morphology and function when heterologously expressed (Q49239818) (← links)
- Polycystin-2 is an essential ion channel subunit in the primary cilium of the renal collecting duct epithelium. (Q49329276) (← links)
- The Genetic and Cellular Basis of Autosomal Dominant Polycystic Kidney Disease-A Primer for Clinicians (Q50023752) (← links)
- Ciliary Mechanisms of Cyst Formation in Polycystic Kidney Disease (Q51093238) (← links)
- Polycystin 1 loss of function is directly linked to an imbalance in G-protein signaling in the kidney. (Q52659737) (← links)
- Adhesion GPCRs in Kidney Development and Disease. (Q52691279) (← links)
- Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing (Q57591372) (← links)
- Polycystin-1, the product of the polycystic kidney disease gene PKD1, is post-translationally modified by palmitoylation (Q58328353) (← links)
- Dopamine receptor antagonists as potential therapeutic agents for ADPKD (Q64065996) (← links)
- Polycystic kidney disease: Pathogenic missense mutations result in defective trafficking of polycystin-1 to cilia (Q86049111) (← links)
- Retromer associates with the cytoplasmic amino-terminus of polycystin-2 (Q88561954) (← links)
- TRPP2 dysfunction decreases ATP-evoked calcium, induces cell aggregation and stimulates proliferation in T lymphocytes (Q90081479) (← links)
- Polycystin 2 regulates mitochondrial Ca2 signaling, bioenergetics, and dynamics through mitofusin 2 (Q91832389) (← links)
- Tulp3 Regulates Renal Cystogenesis by Trafficking of Cystoproteins to Cilia (Q91866626) (← links)
- Autosomal dominant polycystic kidney disease (Q92019794) (← links)
- The ion channel function of polycystin-1 in the polycystin-1/polycystin-2 complex (Q92807475) (← links)
- Identification of ADPKD-Related Genes and Pathways in Cells Overexpressing PKD2 (Q92921933) (← links)