cystic fibrosis transmembrane conductance regulator, partial [Homo sap - Protein

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Loss of CFTR Reverses Senescence Hallmarks in SARS-CoV-2 Infected Bronchial Epithelial Cells. [Int J Mol Sci. 2024]
Loss of CFTR Reverses Senescence Hallmarks in SARS-CoV-2 Infected Bronchial Epithelial Cells.
Merigo F, Lagni A, Boschi F, Bernardi P, Conti A, Plebani R, Romano M, Sorio C, Lotti V, Sbarbati A. Int J Mol Sci. 2024 Jun 4; 25(11). Epub 2024 Jun 4.
Insights and considerations on CFTR variant reporting in a study of cystic fibrosis patients in Saudi Arabia CFTR 1548del G and 1549del G: Navigating the discovery of novel mutations. [Saudi Med J. 2024]
Insights and considerations on CFTR variant reporting in a study of cystic fibrosis patients in Saudi Arabia CFTR 1548del G and 1549del G: Navigating the discovery of novel mutations.
Al Abdulsalam EA. Saudi Med J. 2024 May; 45(5):541.
Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and airway epithelial cells. [Cell Rep Med. 2024]
Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and airway epithelial cells.
Bulcaen M, Kortleven P, Liu RB, Maule G, Dreano E, Kelly M, Ensinck MM, Thierie S, Smits M, Ciciani M, et al. Cell Rep Med. 2024 May 21; 5(5):101544. Epub 2024 May 1.

RefSeq genomic sequence
See the genomic reference sequence for the CFTR gene (NG_016465.4).
RefSeq protein
See the reference protein sequence for cystic fibrosis transmembrane conductance regulator (NP_000483.3).

Nucleotide
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cystic fibrosis transmembrane conductance regulator, partial [Homo sapiens]
cystic fibrosis transmembrane conductance regulator, partial [Homo sapiens]
gi|732666180|gb|AIZ78009.1|

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