Pages that link to "Q37277637"

The following pages link to Update on gene modifiers in cystic fibrosis (Q37277637):

Displaying 48 items.

• SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy (Q24630041) (← links)
• A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studies. (Q30425302) (← links)
• Changes in transcriptome of native nasal epithelium expressing F508del-CFTR and intersecting data from comparable studies (Q30608402) (← links)
• CFTR is a negative regulator of NFkappaB mediated innate immune response (Q33413105) (← links)
• A novel approach to analyze gene expression data demonstrates that the DeltaF508 mutation in CFTR downregulates the antigen presentation pathway (Q33521562) (← links)
• Saturation of the Human Phenome (Q33885880) (← links)
• Only connect: personal genomics and the future of American medicine (Q33983987) (← links)
• Synergistic post-transcriptional regulation of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) by miR-101 and miR-494 specific binding (Q34058721) (← links)
• Emergent Properties of Proteostasis in Managing Cystic Fibrosis (Q34576386) (← links)
• Tgf-β1 inhibits Cftr biogenesis and prevents functional rescue of ΔF508-Cftr in primary differentiated human bronchial epithelial cells. (Q34721046) (← links)
• High rate of Exophiala dermatitidis recovery in the airways of patients with cystic fibrosis is associated with pancreatic insufficiency (Q34741388) (← links)
• Plasma lipidomics reveals potential prognostic signatures within a cohort of cystic fibrosis patients. (Q34776256) (← links)
• Pathway prediction by bioinformatic analysis of the untranslated regions of the CFTR mRNA. (Q34967307) (← links)
• Plasma TGF-β₁ in pediatric cystic fibrosis: potential biomarker of lung disease and response to therapy. (Q35046565) (← links)
• Polymorphisms in the glutathione pathway modulate cystic fibrosis severity: a cross-sectional study (Q35110113) (← links)
• The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients. (Q35113309) (← links)
• Tgf-beta downregulation of distinct chloride channels in cystic fibrosis-affected epithelia (Q35287714) (← links)
• The porcine chloride channel calcium-activated family member pCLCA4a mirrors lung expression of the human hCLCA4. (Q35768133) (← links)
• Association of TNF-α Gene Variants With Clinical Manifestation of Cystic Fibrosis Patients of Iranian Azeri Turkish Ethnicity (Q35862037) (← links)
• Mapping genetic determinants of host susceptibility to Pseudomonas aeruginosa lung infection in mice (Q36014949) (← links)
• Omics approaches in cystic fibrosis research: a focus on oxylipin profiling in airway secretions (Q36112019) (← links)
• Metabolomic profiling of regulatory lipid mediators in sputum from adult cystic fibrosis patients. (Q36142593) (← links)
• In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis (Q36322032) (← links)
• The influence of genetics on cystic fibrosis phenotypes (Q36526522) (← links)
• From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations (Q36574664) (← links)
• Transforming growth factor-β1 impairs CFTR-mediated anion secretion across cultured porcine vas deferens epithelial monolayer via the p38 MAPK pathway (Q37234581) (← links)
• Genomic, tissue expression, and protein characterization of pCLCA1, a putative modulator of cystic fibrosis in the pig (Q37422985) (← links)
• Modifier genes as therapeutics: the nuclear hormone receptor Rev Erb alpha (Nr1d1) rescues Nr2e3 associated retinal disease (Q37539468) (← links)
• Modifier genes in Mendelian disorders: the example of cystic fibrosis (Q37822861) (← links)
• Therapeutics Development for Cystic Fibrosis: A Successful Model for a Multisystem Genetic Disease (Q37827865) (← links)
• Mouse models of cystic fibrosis: phenotypic analysis and research applications (Q37887172) (← links)
• Molecular testing for cystic fibrosis carrier status practice guidelines: recommendations of the National Society of Genetic Counselors (Q38135327) (← links)
• Effect of residential proximity to major roadways on cystic fibrosis exacerbations (Q39578759) (← links)
• Current Concepts and Controversies in Innate Immunity of Cystic Fibrosis Lung Disease. (Q40473713) (← links)
• Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia (Q41212056) (← links)
• Airway Surface Dehydration by Transforming Growth Factor β (TGF-β) in Cystic Fibrosis Is Due to Decreased Function of a Voltage-dependent Potassium Channel and Can Be Rescued by the Drug Pirfenidone. (Q43173804) (← links)
• Cystic fibrosis transmembrane conductance regulator gene mutations and glutathione S-transferase null genotypes in cystic fibrosis patients in Brazil (Q43555873) (← links)
• Cystic fibrosis testing 8 years on: Lessons learned from carrier screening and sequencing analysis (Q43725303) (← links)
• Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population (Q46970170) (← links)
• microRNA-145 Antagonism Reverses TGF-β Inhibition of F508del CFTR Correction in Airway Epithelia. (Q47302859) (← links)
• TGFβ as a therapeutic target in cystic fibrosis. (Q47822059) (← links)
• RNAi in Respiratory Diseases (Q58061971) (← links)
• CFTR dysfunction increases endoglin and TGF-β signaling in airway epithelia (Q64106543) (← links)
• Phenotyping ciliary dynamics and coordination in response to CFTR-modulators in Cystic Fibrosis respiratory epithelial cells (Q64110019) (← links)
• Subacute TGFβ expression drives inflammation, goblet cell hyperplasia, and pulmonary function abnormalities in mice with effects dependent on CFTR function (Q64376984) (← links)
• Pancreatitis in cystic fibrosis: association with genotype and pancreatic status (Q84703925) (← links)
• Cystic Fibrosis: Translating Molecular Mechanisms into Effective Therapies (Q88891870) (← links)
• Losartan Rescues Inflammation-related Mucociliary Dysfunction in Relevant Models of Cystic Fibrosis (Q90715404) (← links)