Pages that link to "Q41111670"
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The following pages link to Peripheral protein quality control removes unfolded CFTR from the plasma membrane (Q41111670):
Displaying 50 items.
- Mechanisms of CFTR Folding at the Endoplasmic Reticulum (Q21129277) (← links)
- Molecular Chaperones as Targets to Circumvent the CFTR Defect in Cystic Fibrosis (Q21129282) (← links)
- Dab2 is a key regulator of endocytosis and post-endocytic trafficking of the cystic fibrosis transmembrane conductance regulator (Q24293214) (← links)
- Disruption of cytokeratin-8 interaction with F508del-CFTR corrects its functional defect (Q24295031) (← links)
- Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations (Q24296610) (← links)
- DNAJs: more than substrate delivery to HSPA (Q26801509) (← links)
- Control of cystic fibrosis transmembrane conductance regulator membrane trafficking: not just from the endoplasmic reticulum to the Golgi (Q26824750) (← links)
- Ubiquitin on the move: the ubiquitin modification system plays diverse roles in the regulation of endoplasmic reticulum- and plasma membrane-localized proteins (Q26849500) (← links)
- Quality control and fate determination of Hsp90 client proteins (Q26853052) (← links)
- Protein homeostasis at the plasma membrane (Q27009009) (← links)
- The delicate balance between secreted protein folding and endoplasmic reticulum-associated degradation in human physiology (Q27015793) (← links)
- A yeast phenomic model for the gene interaction network modulating CFTR-ΔF508 protein biogenesis. (Q27931694) (← links)
- CFTR Modulators: Shedding Light on Precision Medicine for Cystic Fibrosis (Q28073996) (← links)
- Airway hydration and COPD (Q28082617) (← links)
- Approaches for defining the Hsp90-dependent proteome (Q28247643) (← links)
- Role of the ubiquitin system in regulating ion transport (Q28296575) (← links)
- Disulfide bonds in ER protein folding and homeostasis (Q28300205) (← links)
- Myotonia congenita mutation enhances the degradation of human CLC-1 chloride channels (Q28486132) (← links)
- Functional rescue of a kidney anion exchanger 1 trafficking mutant in renal epithelial cells (Q28487020) (← links)
- Selective high-level expression of epsin 3 in gastric parietal cells, where it is localized at endocytic sites of apical canaliculi (Q28511738) (← links)
- Stabilization of integrin-linked kinase by the Hsp90-CHIP axis impacts cellular force generation, migration and the fibrotic response (Q28512119) (← links)
- Involvement of the Cdc42 pathway in CFTR post-translational turnover and in its plasma membrane stability in airway epithelial cells (Q28544026) (← links)
- Ribosomal Stalk Protein Silencing Partially Corrects the ΔF508-CFTR Functional Expression Defect (Q28551966) (← links)
- The silent codon change I507-ATC->ATT contributes to the severity of the ΔF508 CFTR channel dysfunction (Q28658805) (← links)
- Augmentation of CFTR maturation by S-nitrosoglutathione reductase (Q30277961) (← links)
- S-Nitrosothiols increases cystic fibrosis transmembrane regulator expression and maturation in the cell surface (Q30408475) (← links)
- S-Nitrosylation signaling regulates cellular protein interactions (Q30412936) (← links)
- Development of CFTR Structure (Q30421217) (← links)
- Rare mutations in renal sodium and potassium transporter genes exhibit impaired transport function (Q33557328) (← links)
- The Ubiquitin Ligase CHIP Integrates Proteostasis and Aging by Regulation of Insulin Receptor Turnover (Q33606931) (← links)
- Alteration of protein function by a silent polymorphism linked to tRNA abundance (Q33693618) (← links)
- Synergy-based small-molecule screen using a human lung epithelial cell line yields ΔF508-CFTR correctors that augment VX-809 maximal efficacy. (Q33742766) (← links)
- The Hsc/Hsp70 Co-Chaperone Network Controls Antigen Aggregation and Presentation during Maturation of Professional Antigen Presenting Cells (Q33809132) (← links)
- Stabilizing rescued surface-localized δf508 CFTR by potentiation of its interaction with Na( )/H( ) exchanger regulatory factor 1. (Q33843016) (← links)
- Decoding F508del misfolding in cystic fibrosis (Q33912624) (← links)
- Dysfunctional CFTR alters the bactericidal activity of human macrophages against Pseudomonas aeruginosa (Q33916871) (← links)
- ER stress-induced clearance of misfolded GPI-anchored proteins via the secretory pathway (Q34001064) (← links)
- Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner (Q34033437) (← links)
- The interaction between the first transmembrane domain and the thumb of ASIC1a is critical for its N-glycosylation and trafficking (Q34064808) (← links)
- Down-Regulation of Shadoo in Prion Infections Traces a Pre-Clinical Event Inversely Related to PrPSc Accumulation (Q34082684) (← links)
- Cystic fibrosis transmembrane conductance regulator (CFTR) potentiators protect G551D but not ΔF508 CFTR from thermal instability (Q34155612) (← links)
- A microRNA network regulates expression and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulator (Q34291809) (← links)
- A chaperone trap contributes to the onset of cystic fibrosis (Q34305005) (← links)
- A genomic signature approach to rescue ΔF508-cystic fibrosis transmembrane conductance regulator biosynthesis and function (Q34305593) (← links)
- The C8ORF38 homologue Sicily is a cytosolic chaperone for a mitochondrial complex I subunit (Q34333891) (← links)
- Quality control for unfolded proteins at the plasma membrane (Q34412404) (← links)
- Genomic heat shock element sequences drive cooperative human heat shock factor 1 DNA binding and selectivity (Q34430972) (← links)
- Pharmacological Correctors of Mutant CFTR Mistrafficking (Q34444239) (← links)
- Rescue of murine F508del CFTR activity in native intestine by low temperature and proteasome inhibitors (Q34532897) (← links)
- Emergent Properties of Proteostasis in Managing Cystic Fibrosis (Q34576386) (← links)