Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations (Q83482552)

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scientific article published on February 26, 2011

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English	Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations	scientific article published on February 26, 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

21354377

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

title

Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations (English)

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stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

main subject

cystic fibrosis

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based on heuristic

inferred from title

author name string

A. Geborek

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1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21354377

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25 November 2024

L. Hjelte

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2

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Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21354377

retrieved

25 November 2024

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

21354377

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21354377

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25 November 2024

publication date

26 February 2011

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Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

full work available at URL

http://www.cysticfibrosisjournal.com/article/S1569199311000087/pdf

file format

PDF

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21354377

retrieved

25 November 2024

https://api.elsevier.com/content/article/PII:S1569199311000087?httpAccept=text/xml

1 reference

stated in

Crossref

DOI

10.1016/J.JCF.2011.01.005

reference URL

https://api.crossref.org/works/10.1016/J.JCF.2011.01.005

retrieved

25 November 2024

https://api.elsevier.com/content/article/PII:S1569199311000087?httpAccept=text/plain

1 reference

stated in

Crossref

DOI

10.1016/J.JCF.2011.01.005

reference URL

https://api.crossref.org/works/10.1016/J.JCF.2011.01.005

retrieved

25 November 2024

published in

Journal of Cystic Fibrosis

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

volume

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

page(s)

187-192

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stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

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Genotype and phenotype in cystic fibrosis

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Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

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Cystic fibrosis transmembrane conductance regulator (CFTR) activity in nasal epithelial cells from cystic fibrosis patients with severe genotypes

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C-terminal truncations destabilize the cystic fibrosis transmembrane conductance regulator without impairing its biogenesis. A novel class of mutation

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Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden

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Spectrum of mutations in the CFTR gene of patients with classical and atypical forms of cystic fibrosis from southwestern Sweden: identification of 12 novel mutations

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Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

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Cystic fibrosis genotype and assessing rates of decline in pulmonary status

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Identifiers

DOI

10.1016/J.JCF.2011.01.005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

PubMed publication ID

21354377

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21354377

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21354377%20AND%20SRC:MED&resulttype=core&format=json

retrieved

23 January 2020

 

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