[PDF] Top 20 Structure and function of the cystic fibrosis transmembrane conductance regulator
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Structure and function of the cystic fibrosis transmembrane conductance regulator
... 7 and an analysis of the cDNA sequence has shown that the gene product, the CFTR protein, consists of 1,480 amino acids ...on the hydropathy analysis of the ... See full document
8
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 ... See full document
7
Function and expression of cystic fibrosis transmembrane conductance regulator after small intestinal transplantation in mice.
... transection of the intestinal wall along with intrinsic neurons, complete extrinsic autonomic denervation, and the disruption of lymphatic drainage, or ischemia–reperfusion injury ... See full document
9
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 ... See full document
11
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 ... See full document
7
Surfactant protein a in cystic fibrosis: supratrimeric structure and pulmonary outcome.
... to the significant number of different naturally occurring structural organizational forms of SP-A, the desirable number of subjects in some of the groups were lower than ... See full document
7
Diagnosis, Prognosis and Personalized Treatment of Cystic Fibrosis
... CFTR structure determined by electron cryomicroscopy ...molecular structure of human CFTR determined in the dephosphorylated, ATP-free ...amino-acids transmembrane glycoprotein ... See full document
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J. bras. pneumol. vol.38 número1 en v38n1a08
... determine the effects that mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene and deletion of the glutathione ... See full document
7
Mutações no gene cystic fibrosis transmembrane conductance regulator em um centro de referência para a fibrose cística.
... 17. Furgeri DT, Marson FA, Ribeiro AF, Bertuzzo CS. Association between the IVS4G>T mutation in the TCF7L2 gene and susceptibility to diabetes in cystic fibrosis patients. BMC Res ... See full document
7
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 ... See full document
11
Correlation of apical fluid-regulating channel proteins with lung function in human COPD lungs.
... channels and chronic obstructive pulmonary diseases (COPD) are emerging through animal model and in vitro ...proteins and lung function in COPD remain to be ...(ENaC), cystic ... See full document
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Mechanisms of CFTR functional variants that impair regulated bicarbonate permeation and increase risk for pancreatitis but not for cystic fibrosis.
... modeled the molecular structure, and studied the dynamics, of wild type (WT) and mutated CFTR ...Because the effective van der Waals radius of chloride ...that ... See full document
15
The Cystic Fibrosis Transmembrane Regulator (CFTR) in the Kidney
... The cystic fibrosis transmembrane regulator (CFTR) is a Cl − ...Mutations of this transporter lead to a defect of chloride secretion by epithelial cells causing the ... See full document
8
Proteomic identification of calumenin as a G551D-CFTR associated protein.
... Cystic fibrosis (CF) is the most common lethal autosomal recessive disease in the Caucasian ...in the cystic fibrosis transmembrane conductance ... See full document
10
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
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 ... See full document
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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
Rev. Nutr. vol.28 número4
... to the categorical outcome, the Chi-square test of heterogeneity was ...with the Fisher test when there were estimated values <5 in more than 20% of the ...outcome, the ... See full document
12
Radiol Bras vol.48 número6
... practice. The use of MRI for imaging of the thorax, however, has been historically considered of limited value, despite the effort of physicists and radiologists to ... See full document
2
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
... evaluates the impact of the 2007 expansion of the Bolsa Família program to families with youths aged 16 to 17 years (entitled Benefício Variável Jovem) on the time allocation ... See full document
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