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2.
Neurogastroenterol Motil ; 20(4): 285-90, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18036136

ABSTRACT

Although dysphagia is a common complaint of patients with Wilson's disease (WD) and pneumonia is an important cause of death in these patients, swallowing function remains an underinvestigated field in this condition. The aim of this study was to characterize swallowing dynamics in WD patients. Eight WD patients and 15 age-matched controls underwent scintigraphic evaluation of oral and pharyngeal deglutition. Patients had significantly slower oral transit (P = 0.008) and a greater percentage of oral residue (P = 0.006) when compared to controls. Two of eight patients were free of neurological symptoms at time of examination. Impaired oropharyngeal function was found in patients without dysphagia and without neurological symptoms. Our findings indicate that WD may present with objective swallowing dysfunction, even in the absence of neurological manifestations. Further studies are necessary to investigate the impact of this dysfunction on morbidity and mortality in WD.


Subject(s)
Deglutition Disorders/etiology , Hepatolenticular Degeneration/complications , Adult , Deglutition Disorders/diagnosis , Female , Hepatolenticular Degeneration/physiopathology , Humans , Male , Middle Aged , Radionuclide Imaging
3.
Mem Inst Oswaldo Cruz ; 97(3): 335-41, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12048561

ABSTRACT

The great expansion in the number of genome sequencing projects has revealed the importance of computational methods to speed up the characterization of unknown genes. These studies have been improved by the use of three dimensional information from the predicted proteins generated by molecular modeling techniques. In this work, we disclose the structure-function relationship of a gene product from Leishmania amazonensis by applying molecular modeling and bioinformatics techniques. The analyzed sequence encodes a 159 amino acids polypeptide (estimated 18 kDa) and was denoted LaPABP for its high homology with poly-A binding proteins from trypanosomatids. The domain structure, clustering analysis and a three dimensional model of LaPABP, basically obtained by homology modeling on the structure of the human poly-A binding protein, are described. Based on the analysis of the electrostatic potential mapped on the model's surface and conservation of intramolecular contacts responsible for folding stabilization we hypothesize that this protein may have less avidity to RNA than it's L. major counterpart but still account for a significant functional activity in the parasite. The model obtained will help in the design of mutagenesis experiments aimed to elucidate the mechanism of gene expression in trypanosomatids and serve as a starting point for its exploration as a potential source of targets for a rational chemotherapy.


Subject(s)
Leishmania/chemistry , Protozoan Proteins/chemistry , RNA-Binding Proteins/chemistry , Animals , Humans , Leishmania/genetics , Models, Molecular , Protein Structure, Secondary , Protein Structure, Tertiary , Protozoan Proteins/genetics , RNA-Binding Proteins/genetics , Sequence Alignment , Sequence Analysis, Protein , Sequence Homology , Trypanosoma/chemistry , Trypanosoma/genetics
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