Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
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Showing 1 to 5 of 5 for “"EIF4G1"”.
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Identificação de parceiros funcionais e propriedades do fator EIF4E5, homólogo do fator de iniciação da tradução EIF4E (EIF4E5) de Leishmania infantum
… que o EIF4E5 interage especificadamente com o EIF4G1, homólogo de outra subunidade do complexo eIF4F, o eIF4G. Outras interações com proteínas de modificação de mRNAs e ligadas a vias de sinalização também foram identificadas, mas várias destas interações foram abolidas quando foi mutado um …
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Identifying novel proteins in translation complex by using analytical ultracentrifugation with fluorescent detection system
… the translation initiation complex: mRNA, eIF4E, eIF4G1/eIF4G2, PAB1, 40S and 60S ribosomal components. Using GFP fused to about half of the 41 putative novel proteins of the components of the 78S translation complex, we were able to identify at five new proteins, SBP1, SLF1, PUB1, SUP35 and SSD1 …
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Identification and stoichiometric analysis of the monosomal translational complex
… components of the closed-loop structure, eIF4E, eIF4G1/eIF4G2 and PAB1. The abundance of 77S complexes decreased with translational defects and following the stresses that cause translational stoppage. By quantitating the abundance of the 77S complex in response to different stress conditions, I …
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The identification and characterization of the interaction between Upf1 and PAB1 during nonsense-mediated decay & the identification of novel protein complexes associated with translation termination factor eRF1
… contained the closed-loop components eIF4E, eIF4G1, and PABl. However, stoichiometric analysis revealed that the complexes greater than 28S were comprised mostly of free ribosomal subunits associated with eRF1. Glucose deprivation and cycloheximide stress treatments revealed that these …
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Heredity in Parkinson's disease. From rare mutations to common genetic risk factors.
… or parkinsonism was examined. The SNCA, LRRK2, EIF4G1, VPS35, PINK1, ATXN2 and ATXN3 genes were analyzed in all probands; the PARKIN, PINK1 and DJ1 genes were tested in a subgroup of 23 patients with young onset or marked heredity. DNA from the brain tissue of 7 patients with parkinsonism was …