27 results on '"Zielenski, Julian"'
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2. Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?
3. Role of Cystic Fibrosis Transmembrane Conductance Regulator in Patients With Chronic Sinopulmonary Disease
4. A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis Genetic modifier studies
5. Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis
6. Genetic Modifiers of Liver Disease in Cystic Fibrosis
7. CFTR2: DEFINING THE CLINICAL AND FUNCTIONAL CONSEQUENCES OF CFTR MUTATIONS: S11.1
8. FINDING GENETIC MODIFIERS OF CF LUNG DISEASE USING GENOMEWIDE LINKAGE: S15.2
9. Complex two-gene modulation of lung disease severity in children with cystic fibrosis
10. Primary Sclerosing Cholangitis in Childhood is Associated with Abnormalities in Cystic Fibrosis–Mediated Chloride Channel Function
11. PhenCode: Connecting ENCODE Data With Mutations and Phenotype
12. Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X
13. Mutations in the Cystic Fibrosis Transmembrane Regulator Gene and In Vivo Transepithelial Potentials
14. Cystic Fibrosis Transmembrane Conductance Regulator Function Is Suppressed in Cigarette Smokers
15. Genetic Modifiers of Lung Disease in Cystic Fibrosis
16. TWO-TIERED IMMUNOREACTIVE TRYPSINOGEN-BASED NEWBORN SCREENING FOR CYSTIC FIBROSIS IN COLORADO: SCREENING EFFICACY AND DIAGNOSTIC OUTCOMES
17. Clinical Manifestations of Cystic Fibrosis Among Patients With Diagnosis in Adulthood*
18. Airway Inflammation and Infection in Congenital Bilateral Absence of the Vas Deferens
19. α1-Antitrypsin Deficiency Alleles in Cystic Fibrosis Lung Disease
20. Characterization of disease-associated mutations affecting an exonic splicing enhancer and two cryptic splice sites in exon 13 of the cystic fibrosis transmembrane conductance regulator gene
21. Glucose intolerance in children with cystic fibrosis
22. Genotype and Phenotype in Cystic Fibrosis
23. An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis
24. Proportion of Cystic Fibrosis Gene Mutations Not Detected by Routine Testing in Men With Obstructive Azoospermia
25. Uncertainty in the diagnosis of cystic fibrosis: Possible role of in vivo nasal potential difference measurements
26. Screening for genetic mutations
27. Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations
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