[PDF] Top 20 The Cystic Fibrosis Transmembrane Regulator (CFTR) in the Kidney
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The Cystic Fibrosis Transmembrane Regulator (CFTR) in the Kidney
... The cystic fibrosis transmembrane regulator (CFTR) is a Cl − ...causing the Cystic Fibrosis disease (CF). In spite of the high expression of CFTR ... See full document
8
J. bras. pneumol. vol.38 número1 en v38n1a08
... for the detection of the ∆F508 mutation in the cystic fibrosis transmembrane conductance regulator ( CFTR ) gene, as well as of the deletion of glutathione ... See full document
7
Characterization of mRNA dysfunctional mechanisms associated with the genetic disease cystic fibrosis
... with the advent of next generation sequencing complete sequencing of large disease- associated genes and intronic regions is economically not ...is the case of cystic fibrosis ... See full document
169
PDF EN Jornal Brasileiro de Pneumologia 1 8 english
... determine the effects that mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene and deletion of the glutathione S-transferase (GST) genes mu-1 ... See full document
7
Structure and function of the cystic fibrosis transmembrane conductance regulator
... of cystic fibrosis physiopathol- ogy. The mutations expected to cause the most severe disease are those that affect the ability of CFTR to function both as a chlo- ride channel and as a ... See full document
8
Vitamin K status in cystic fibrosis patients
... is the most common autosomal recessive genetic disease in the Caucasian popu- lation [Hecker and Aris ...mutation in the CFTR gene (cystic fi- brosis transmembrane ... See full document
5
Adeno-associated virus for cystic fibrosis gene therapy
... as cystic fibrosis. Cystic fibrosis is a severe autosomal recessive disease affecting one in 2500 live births in the white population, caused by mutation of the ... See full document
9
Function and expression of cystic fibrosis transmembrane conductance regulator after small intestinal transplantation in mice.
... from the mucosae of jejunal graft, host jejunum, and control jejunum was extracted using Trizol Reagent (Invitrogen) according to the manufacture’s ...instruction. The concentrations of all RNA ... See full document
9
Proteomic identification of calumenin as a G551D-CFTR associated protein.
... Cystic fibrosis (CF) is the most common lethal autosomal recessive disease in the Caucasian ...mutations in the cystic fibrosis transmembrane ... See full document
10
Mutações do gene cystic fibrosis transmembrane conductance regulator e deleções dos genes glutationa S-transferase em pacientes com fibrose cística no Brasil.
... determine the effects that mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene and deletion of the glutathione S-transferase (GST) genes mu-1 ... See full document
7
Correlation of apical fluid-regulating channel proteins with lung function in human COPD lungs.
... and in vitro ...function in COPD remain to be ...(ENaC), cystic fibrosis transmembrane conductance regulator (CFTR), and aquaporin 5 (AQP5) proteins in human COPD lungs ... See full document
10
Mutações no gene cystic fibrosis transmembrane conductance regulator em um centro de referência para a fibrose cística.
... 4. Sousa M, Servidoni MF, Vinagre AM, Ramalho AS, Bonadia LC, Felício V, et al. Measurements of CFTR- mediated Cl-secretion in human rectal biopsies constitute a robust biomarker for cystic fibrosis ... See full document
7
Prevalência da mutação ΔF508 no gene cystic fibrosis transmembrane conductance regulator em pacientes com fibrose cística em um centro de referência no Brasil.
... verify the presence of ΔF508 mutation in the cystic fibrosis transmembrane conductance regulator gene among patients with cystic fibrosis diagnosed by ... See full document
4
Pesquisa da mutação F508del como primeiro passo no diagnóstico molecular de fibrose cística.
... determine the relevance of screening for the F508del mutation of the cystic fibrosis transmembrane conductance regulator gene as a first step in the genetic ... See full document
11
J. bras. pneumol. vol.35 número2
... with cystic fibrosis (cystic fibrosis transmembrane conductance regulator gene mutation dF508 homozygous) presented with right-sided chest pain and increasing ...with the ... See full document
3
J. bras. pneumol. vol.39 número3
... determine the relevance of screening for the F508del mutation of the cystic fibrosis transmembrane conductance regulator gene as a first step in the genetic ... See full document
11
The Impact of the Expansion of the Bolsa Familia Program on the Time Allocation of Youths And Their Parents Lia Chitolina Miguel Nathan Foguel Naercio Menezes-Filho
... household, the program caused an increase of more than 11 percentage points in the probability of attending ...increase in the estimated impact is the fact that his/her family is ... See full document
39
Field Cancerisation of the Upper Aerodigestive Tract: Screening for Second Primary Cancers of the Oesophagus in Cancer Survivors
... are the main causes of squamous cell cancers of the upper aerodigestive ...of the oesophagus, head and neck region, and lungs (‘ield ...of the oesophagus. The risk of second primary ... See full document
8
Oil Tanker Transportation In The Russian Arctic
... of the Russian Arctic includes Barents sea, Kara sea, Laptev sea, East Siberian sea and Chukchi ...to the different estimations the amount of hydrocarbon resources in the Russian Arctic ... See full document
7
Dyspnea perception in cystic fibrosis patients
... with the paired samples ...with the Wilcoxon signed-rank ...with the log rank test to compare the completion of the dyspnea perception test during inspiratory resistive ...compare ... See full document
7
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