Sökning: "Anders S. Byström"
Visar resultat 1 - 5 av 7 avhandlingar innehållade orden Anders S. Byström.
1. "De discrimine philosophiae criticae et disciplinae, quae ab identitate nomen habet" quaestionem, quam ... publice defensurus mag. Andreas Södermark ... respondente Andrea Byström jemtlando tertio disputationis actu post meridiano In auditorio Gustauiano die martii 23 a:o 1815., P. 3
Sammanfattning : .... LÄS MER
2. Functional aspects of wobble uridine modifications in yeast tRNA
Sammanfattning : Transfer RNAs (tRNA) function as adaptor molecules in the translation of mRNA into protein. These adaptor molecules require modifications of a subset of their nucleosides for optimal function. The most frequently modified nucleoside in tRNA is position 34 (wobble position), and especially uridines present at this position. LÄS MER
3. Functional aspects of modified nucleosides in tRNA
Sammanfattning : Transfer ribonucleic acids (tRNAs) are extensively modified, especially their anticodon loops. Modifications at position 34 (wobble base) and 37 in these loops affect the tRNAs’ decoding ability, while modifications outside the anticodon loops, e.g. m1A58 of tRNAMeti, may be crucial for tRNA structure or stability. LÄS MER
4. Investigation of RNase P active site residues and catalytic domain interaction
Sammanfattning : RNase P is an essential endoribonuclease responsible for the maturation of the tRNA 5’end. The RNase P family encompasses the ribozyme based, RNase P RNP, and proteinaceous RNase P (PRORP). The ribozyme based RNase P is widely distributed in most species while PRORP has so far mainly been found in some eukaryotic cells. LÄS MER
5. Physiological consequences of Elongator complex inactivation in Eukaryotes
Sammanfattning : Mutations found in genes encoding human Elongator complex subunits have been linked to neurodevelopmental disorders such as familial dysautonomia (FD), rolandic epilepsy and amyotrophic lateral sclerosis. In addition, loss-of-function mutations in genes encoding Elongator complex subunits cause defects in neurodevelopment and reduced neuronal function in both mice and nematodes. LÄS MER