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Publication details

Document type
Journal articles

Document subtype
Full paper

Title
Theranostics by testing CFTR modulators in patient-derived materials: The current status and a proposal for subjects with rare CFTR mutations

Participants in the publication
Margarida D. Amaral (Author)
Dep. Química e Bioquímica
BIOISI - Instituto de Biossistemas e Ciências Integrativas
Kris de Boeck (Author)
Jane C. Davies (Author)
Kris de Boeck (Author)
Pavel Drevinek (Author)
Stuart Elborn (Author)
Eitan Kerem (Author)
Tim Lee (Author)

Date of Publication
2019-09

Where published
Journal of Cystic Fibrosis

Publication Identifiers
ISSN - 1569-1993

Publisher
Elsevier BV

Volume
18
Number
5

Number of pages
7
Starting page
685
Last page
692

Document Identifiers
DOI - https://doi.org/10.1016/j.jcf.2019.06.010
URL - http://dx.doi.org/10.1016/j.jcf.2019.06.010

Rankings
SCIMAGO Q1 (2018) - 1.57 - Pulmonary and Respiratory Medicine
SCOPUS Q1 (2017) - 1.587 - Pulmonary and Respiratory Medicine


Export

APA
Margarida D. Amaral, Kris de Boeck, Jane C. Davies, Kris de Boeck, Pavel Drevinek, Stuart Elborn, Eitan Kerem, Tim Lee, (2019). Theranostics by testing CFTR modulators in patient-derived materials: The current status and a proposal for subjects with rare CFTR mutations. Journal of Cystic Fibrosis, 18, 685-692. ISSN 1569-1993. eISSN . http://dx.doi.org/10.1016/j.jcf.2019.06.010

IEEE
Margarida D. Amaral, Kris de Boeck, Jane C. Davies, Kris de Boeck, Pavel Drevinek, Stuart Elborn, Eitan Kerem, Tim Lee, "Theranostics by testing CFTR modulators in patient-derived materials: The current status and a proposal for subjects with rare CFTR mutations" in Journal of Cystic Fibrosis, vol. 18, pp. 685-692, 2019. 10.1016/j.jcf.2019.06.010

BIBTEX
@article{45468, author = {Margarida D. Amaral and Kris de Boeck and Jane C. Davies and Kris de Boeck and Pavel Drevinek and Stuart Elborn and Eitan Kerem and Tim Lee}, title = {Theranostics by testing CFTR modulators in patient-derived materials: The current status and a proposal for subjects with rare CFTR mutations}, journal = {Journal of Cystic Fibrosis}, year = 2019, pages = {685-692}, volume = 18 }