(Q34001834)

English

Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

cystic fibrosis

0 references

Pseudomonas aeruginosa

0 references

1 reference

ORCID Public Data File 2021

author name string

R B Parad

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

C J Gerard

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

D Zurakowski

3

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

D P Nichols

4

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

G B Pier

5

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

language of work or name

0 references

publication date

1 September 1999

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Infection and Immunity

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

67

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

4744-4750

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Random-effects models for longitudinal data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Changes in the normal maximal expiratory flow-volume curve with growth and aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Unbalanced repeated-measures models with structured covariance matrices.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Opsonophagocytic killing antibody to Pseudomonas aeruginosa mucoid exopolysaccharide in older noncolonized patients with cystic fibrosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Identification of the cystic fibrosis gene: genetic analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Pseudomonas aeruginosa alginate in cystic fibrosis sputum and the inflammatory response

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Independent genetic determinants of pancreatic and pulmonary status in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Genetic determination of exocrine pancreatic function in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

5 July 2018

Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

29 October 2018

Relationship of genotype to early pulmonary function in infants with cystic fibrosis identified through neonatal screening.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

29 October 2018

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=96804

29 October 2018

Immunochemical characterization of the mucoid exopolysaccharide of Pseudomonas aeruginosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linked marker haplotypes and the delta F508 mutation in adults with mild pulmonary disease and cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protection against mucoid Pseudomonas aeruginosa in rodent models of endobronchial infections

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis: relationship between clinical status and F508 deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of poor clinical status and heavy exposure to tobacco smoke in patients with cystic fibrosis who are homozygous for the F508 deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype/phenotype association in cystic fibrosis: analyses of the delta F508, R553X, and 3905insT mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation between genotype and phenotype in patients with cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delta F508 genotype does not predict disease severity in an ethnically diverse cystic fibrosis population

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-phenotype correlations in cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population variation of common cystic fibrosis mutations. The Cystic Fibrosis Genetic Analysis Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early pulmonary inflammation in infants with cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cross-sectional and longitudinal studies of naturally occurring antibodies to Pseudomonas aeruginosa in cystic fibrosis indicate absence of antibody-mediated protection and decline in opsonic quality after infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/10456926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/IAI.67.9.4744-4750.1999

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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