The cystic fibrosis and is product CFTR

scientific article published on February 1, 1993

The cystic fibrosis and is product CFTR is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1006/SCEL.1993.1005
P953full work available at URLhttps://api.elsevier.com/content/article/PII:S1043468283710056?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1043468283710056?httpAccept=text/plain
P698PubMed publication ID7680915

P2093author name stringA. Harris
B. E. Argent
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectcystic fibrosisQ178194
P304page(s)37-44
P577publication date1993-02-01
P1433published inSeminars in cell biologyQ27709374
P1476titleThe cystic fibrosis and is product CFTR
P478volume4

Reverse relations

cites work (P2860)
Q28082617Airway hydration and COPD
Q80988310Analysis of most common CFTR mutations in patients affected by nasal polyps
Q35169502Defective adenosine-stimulated cAMP production in cystic fibrosis airway epithelia: a novel role for CFTR in cell signaling
Q89723027Essential oils against bacterial isolates from cystic fibrosis patients by means of antimicrobial and unsupervised machine learning approaches
Q94327353Interventions for promoting participation in shared decision‐making for children and adolescents with cystic fibrosis
Q27937585Inventory and function of yeast ABC proteins: about sex, stress, pleiotropic drug and heavy metal resistance
Q33585358Loss of SLC9A3 decreases CFTR protein and causes obstructed azoospermia in mice
Q42130797Upregulation of CFTR in patients with endometriosis and its involvement in NFκB-uPAR dependent cell migration

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