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403154 CFTR

403154

CFTR

cystic fibrosis transmembrane conductance regulator

protein-coding

Sus scrofa

基因描述

Type Description
Definition cystic fibrosis transmembrane conductance regulator

研究结论

Date Results Publications
2021-02-06 13:58:00 Early pathogenesis of cystic fibrosis gallbladder disease in a porcine model. 32719544
2021-02-02 13:27:00 Acidic Submucosal Gland pH and Elevated Protein Concentration Produce Abnormal Cystic Fibrosis Mucus. 32730755
2020-07-25 10:41:00 In CFTR-knockout airways, the serous acini, collecting ducts, and ciliated ducts fail to transport ions after forskolin stimulation, resulting in the production of smaller volumes of ASL with normal Cl-, Na+, and K+ concentration. 32130033
2016-09-17 10:47:00 Results suggest that acetylcholine does not regulate the activity of the CFTR in tracheal epithelia of pigs which opposes observation from studies using mice airway epithelium. 26286842
2014-11-29 11:26:00 Expression of CFTR-F508del interferes with smooth muscle cell calcium handling and decreases aortic responsiveness. 24183914

名称对应

Type IDs
Synonymous ABCC7
Gene
UniProtKB-ID: CFTR_PIG
UniprotKB: Q6PQZ2
UniParc: UPI000035A9F6
EMBL: DP000017, AY585334
KO: ssc:403154
Nucleutide sequences
EMBL-CDS: AAR16305.1, AAS98211.1
Protein sequencees
RefSeq: NP_001098420.1, XP_020934182.1, XP_020934181.1, XP_020934179.1
Others
UniRef100: UniRef100_Q6PQZ2
UniRef90: UniRef90_Q6PQZ2
UniRef50: UniRef50_P13569
UniGene: Ssc.26325

全选

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研究热度

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