Examples of using CFTR in English and their translations into Spanish
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Official
Cystic fibrosis and CFTR: from learning to living.
Correlation of CFTR gene mutations with the Cl- channel function.
CFTR correctors, a therapy for cystic fibrosis targeted at specific mutations.
The first postulated that the CFTR protein is a Cl- channel.
Spermatozoa were successfully retrieved in 100% of the patients with CFTR mutations.
The CFTR gene is also associated with congenital absence of vas deferens(ARVC).
This gene encodes a protein(CFTR) of 1480 amino acids
The human gene that encodes the CFTR protein was sequenced by Francis Collins and Lap-Chee Tsui.
Secondly, phosphorylation of CFTR by Protein kinase A II should occur in order for the channel to be operational.
subfamily C(CFTR/ MRP)
Cystic fibrosis- see Cystic Fibrosis- CFTR- gene is a potentially fatal disease that is diagnosed in early life due to lung
The patient is positive for the F508del mutation on both alleles of the cystic fibrosis transmembrane conductase regulator(CFTR) gene or the patient has a mutation in the cystic fibrosis transmembrane conductance regulator(CFTR)
this respiratory disease is complex because it involves: 1 a genetic defect with serious consequences on the expression of the CFTR protein, 2 an excessive pulmonary inflammatory response with major disruption of mucus and defenses against bacteria
CFTR is a chloride channel regulated by cAMP,
In 1989, the CFTR gene, implicated in the CF, was isolated.
CFTR is an autosomal recessive gene.
CFTR channels rely on ATP for two main purposes.
Find out more about CFTR science.
Mutations in the CFTR gene altered production,
The examples of aquaporins and CFTR show how the plasma membrane can be selective about what enters