Pages that link to "Q36727301"
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The following pages link to Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2 (Q36727301):
Displaying 50 items.
- Chloride channels as drug targets (Q24601830) (← links)
- Identification of mutations in the putative ATP-binding domain of the adrenoleukodystrophy gene (Q24628731) (← links)
- Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypes (Q24672808) (← links)
- Mutations within the first LSGGQ motif of Ste6p cause defects in a-factor transport and mating in Saccharomyces cerevisiae (Q27936085) (← links)
- A novel SMC protein complex in Schizosaccharomyces pombe contains the Rad18 DNA repair protein (Q28140483) (← links)
- Identification of human Kir2.2 (KCNJ12) gene encoding functional inward rectifier potassium channel in both mammalian cells and Xenopus oocytes (Q28213483) (← links)
- Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (Q28510880) (← links)
- Pharmacological induction of CFTR function in patients with cystic fibrosis: mutation-specific therapy. (Q30350675) (← links)
- Development of CFTR Structure (Q30421217) (← links)
- Regulation of CFTR Cl- ion channels by phosphorylation and dephosphorylation. (Q33602315) (← links)
- Folding and rescue of a cystic fibrosis transmembrane conductance regulator trafficking mutant identified using human-murine chimeric proteins (Q33605591) (← links)
- ATP-independent CFTR channel gating and allosteric modulation by phosphorylation (Q33734745) (← links)
- DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis (Q33854446) (← links)
- Nonsense mutation R1162X of the cystic fibrosis transmembrane conductance regulator gene does not reduce messenger RNA expression in nasal epithelial tissue (Q33909657) (← links)
- Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening. (Q33925348) (← links)
- Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents (Q34080254) (← links)
- A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis (Q34141568) (← links)
- Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding (Q34235099) (← links)
- A single amino acid substitution in CFTR converts ATP to an inhibitory ligand (Q34262494) (← links)
- Proteomic identification of calumenin as a G551D-CFTR associated protein (Q34328753) (← links)
- The cystic fibrosis transmembrane conductance regulator: an intriguing protein with pleiotropic functions (Q34355404) (← links)
- Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels (Q34390399) (← links)
- CFTR: domains, structure, and function (Q34461084) (← links)
- Genetic heterogeneity in familial hyperinsulinism. (Q34470870) (← links)
- The cystic fibrosis transmembrane conductance regulator gene (Q34719664) (← links)
- Association of cystic fibrosis transmembrane conductance regulator gene variants with acute lung injury in African American children with pneumonia*. (Q34755868) (← links)
- Therapeutic approaches to repair defects in deltaF508 CFTR folding and cellular targeting. (Q35012417) (← links)
- Localizing a gate in CFTR. (Q35134541) (← links)
- Orphan missense mutations in the cystic fibrosis transmembrane conductance regulator: A three-step biological approach to establishing a correlation between genotype and phenotype (Q35169295) (← links)
- CFTR! (Q35334619) (← links)
- Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel (Q35399378) (← links)
- Sildenafil (Viagra) corrects DeltaF508-CFTR location in nasal epithelial cells from patients with cystic fibrosis. (Q35537044) (← links)
- Alteration of CFTR transmembrane span integration by disease-causing mutations (Q35579788) (← links)
- Pharmacological approaches to correcting the ion transport defect in cystic fibrosis (Q35627639) (← links)
- Phosphatase inhibitors activate normal and defective CFTR chloride channels (Q35767286) (← links)
- Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manif (Q35821409) (← links)
- Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations. (Q35844736) (← links)
- Processing and function of CFTR-DeltaF508 are species-dependent (Q35991100) (← links)
- Improved fluorescence assays to measure the defects associated with F508del-CFTR allow identification of new active compounds (Q36251047) (← links)
- G551D and G1349D, two CF-associated mutations in the signature sequences of CFTR, exhibit distinct gating defects (Q36296010) (← links)
- Glycans in the intestinal peptide transporter PEPT1 contribute to function and protect from proteolysis (Q36321216) (← links)
- Dynamic association of proteasomal machinery with the centrosome (Q36342153) (← links)
- Reversible silencing of CFTR chloride channels by glutathionylation (Q36412614) (← links)
- CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated state (Q36415724) (← links)
- Assessing the Disease-Liability of Mutations in CFTR (Q36526518) (← links)
- Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia (Q36531655) (← links)
- The multidrug transporter Pdr5 on the 25th anniversary of its discovery: an important model for the study of asymmetric ABC transporters (Q36669332) (← links)
- Characterization of the cystic fibrosis transmembrane conductance regulator in a colonocyte cell line (Q36896230) (← links)
- Cooperative assembly and misfolding of CFTR domains in vivo. (Q37146655) (← links)
- Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators. (Q37312856) (← links)