Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.

Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.

Item
http://www.wikidata.org/entity/Q41547475
A cluster of negative charges at the amino terminal tail of CFTR regulates ATP-dependent channel gatingThe elements of life and medicinesThe complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data.Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practiceCystic fibrosis transmembrane conductance regulator. Structure and function of an epithelial chloride channel.SNaPshot assay for the detection of the most common CFTR mutations in infertile men.The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques.Assessing the Disease-Liability of Mutations in CFTRInfertility in females with cystic fibrosis is multifactorial: evidence from mouse modelsA unified view of cystic fibrosis transmembrane conductance regulator (CFTR) gating: combining the allosterism of a ligand-gated channel with the enzymatic activity of an ATP-binding cassette (ABC) transporterClinical, laboratory and genetic assessment of patients with congenital bilateral absent vas deferens.CELF proteins regulate CFTR pre-mRNA splicing: essential role of the divergent domain of ETR-3.CFTR gene mutations in men with bilateral ejaculatory-duct obstruction and anomalies of the seminal vesicles.Genetic, andrological and clinical characteristics of patients with congenital bilateral absence of the vas deferens.Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.Cystic fibrosis presenting as acute pancreatitis and obstructive azoospermia in a young adult male with a novel mutation in the CFTR gene.Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system
P2860

Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.

Item
http://www.wikidata.org/entity/Q41547475
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh
1996年學術文章
@zh-hant
name
Mutations in the cystic fibros ...... l absence of the vas deferens.
@en
type
label
Mutations in the cystic fibros ...... l absence of the vas deferens.
@en
prefLabel
Mutations in the cystic fibros ...... l absence of the vas deferens.
@en
P1433
P1476
P2093
P304
P31
P356
P433
P478
P577
P5875
P698
P921
P356
P1433
P1476
Mutations in the cystic fibros ...... l absence of the vas deferens.
@en
P2093
P304
P31
P356
P433
P478
P577
P5875
P698
P921