Pages that link to "Q35318538"
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The following pages link to Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation (Q35318538):
Displaying 50 items.
- Differential function of the two nucleotide binding domains on cystic fibrosis transmembrane conductance regulator (Q22010873) (← links)
- MTABC3, a novel mitochondrial ATP-binding cassette protein involved in iron homeostasis (Q22254207) (← links)
- Genomic localization of the human gene for KCNA10, a cGMP-activated K channel (Q24308786) (← links)
- The A2b adenosine receptor mediates cAMP responses to adenosine receptor agonists in human intestinal epithelia (Q24311856) (← links)
- Expression of a renal type I sodium/phosphate transporter (NaPi-1) induces a conductance in Xenopus oocytes permeable for organic and inorganic anions (Q28378848) (← links)
- Regulation of CFTR Cl- ion channels by phosphorylation and dephosphorylation. (Q33602315) (← links)
- Case studies in cholera: lessons in medical history and science. (Q33930013) (← links)
- Flufenamic acid as an ion channel modulator (Q33978847) (← links)
- Phosphate stimulates CFTR Cl- channels (Q34018841) (← links)
- Biochemical status of renal epithelial Na+ channels determines apparent channel conductance, ion selectivity, and amiloride sensitivity (Q34047501) (← links)
- Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulation (Q34115263) (← links)
- Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization (Q34120803) (← links)
- Defective fluid transport by cystic fibrosis airway epithelia (Q34134003) (← links)
- Molecular Biology of Cystic Fibrosis (Q34306869) (← links)
- The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function (Q34489613) (← links)
- The interaction of gut microbes with host ABC transporters (Q34503647) (← links)
- The cystic fibrosis transmembrane conductance regulator gene (Q34719664) (← links)
- Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes (Q35009670) (← links)
- The spectrum of cystic fibrosis mutations (Q35150488) (← links)
- Cell and gene therapy for genetic diseases: inherited disorders affecting the lung and those mimicking sudden infant death syndrome (Q36084447) (← links)
- Efficient expression of CFTR function with adeno-associated virus vectors that carry shortened CFTR genes (Q36287507) (← links)
- Functionally distinct phospho-forms underlie incremental activation of protein kinase-regulated Cl- conductance in mammalian heart (Q36411397) (← links)
- ATP dependence of Na+/H+ exchange. Nucleotide specificity and assessment of the role of phospholipids (Q36417627) (← links)
- Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions (Q36435912) (← links)
- Status of fluid and electrolyte absorption in cystic fibrosis (Q36488263) (← links)
- Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia (Q37140474) (← links)
- Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis (Q37353301) (← links)
- Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency. (Q37694646) (← links)
- ABC proteins protect the human body and maintain optimal health (Q37851290) (← links)
- Research on cystic fibrosis: a journey from the Heart House (Q38578843) (← links)
- EG-VEGF, BV8, and their receptor expression in human bronchi and their modification in cystic fibrosis: Impact of CFTR mutation (delF508). (Q38866990) (← links)
- Treatment of cystic fibrosis based on understanding CFTR. (Q40379266) (← links)
- Gene therapy for the respiratory manifestations of cystic fibrosis (Q40398397) (← links)
- Sequence homologies between nucleotide binding regions of CFTR and G-proteins suggest structural and functional similarities (Q40401846) (← links)
- Molecular basis of epithelial Cl channels. (Q40473234) (← links)
- Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis (Q40488178) (← links)
- Cystic fibrosis transmembrane conductance regulator mediates sulphonylurea block of the inwardly rectifying K+ channel Kir6.1. (Q41037145) (← links)
- Levamisole inhibits intestinal Cl- secretion via basolateral K+ channel blockade (Q41038007) (← links)
- CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates. (Q41056312) (← links)
- Progress in human gene therapy (Q41066768) (← links)
- Cystic fibrosis: How do CFTR mutations cause cystic fibrosis? (Q41072064) (← links)
- Biology of membrane transport proteins (Q41095748) (← links)
- Alternate stimulation of apical CFTR by genistein in epithelia (Q41250130) (← links)
- Effects of lovastatin on trafficking of cystic fibrosis transmembrane conductance regulator in human tracheal epithelium (Q41281567) (← links)
- Pyrophosphate stimulates wild-type and mutant cystic fibrosis transmembrane conductance regulator Cl- channels (Q41306459) (← links)
- Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells (Q41404505) (← links)
- Induction of multidrug resistance downregulates the expression of CFTR in colon epithelial cells (Q41513162) (← links)
- Development and Analysis of Recombinant Adenoviruses for Gene Therapy of Cystic Fibrosis (Q41540042) (← links)
- The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR. (Q41565014) (← links)
- Genetic and immunologic aspects of cystic fibrosis (Q41660557) (← links)