Interférence par ARNUn ARN interférent est un acide ribonucléique (ARN) simple ou double brin dont l'interférence avec un ARN messager spécifique conduit à sa dégradation et à la diminution de sa traduction en protéine. Dans la mesure où l'ARN joue un rôle crucial dans l'expression des gènes, l'ARN interférent permet de bloquer celle-ci en rendant « silencieux » tel ou tel gène. Ce phénomène a été découvert dans les années 1990, valant à Andrew Z. Fire et Craig C. Mello le prix Nobel de physiologie et de médecine en 2006.
Frameshift mutationA frameshift mutation (also called a framing error or a reading frame shift) is a genetic mutation caused by indels (insertions or deletions) of a number of nucleotides in a DNA sequence that is not divisible by three. Due to the triplet nature of gene expression by codons, the insertion or deletion can change the reading frame (the grouping of the codons), resulting in a completely different translation from the original. The earlier in the sequence the deletion or insertion occurs, the more altered the protein.
Distributive shockDistributive shock is a medical condition in which abnormal distribution of blood flow in the smallest blood vessels results in inadequate supply of blood to the body's tissues and organs. It is one of four categories of shock, a condition where there is not enough oxygen-carrying blood to meet the metabolic needs of the cells which make up the body's tissues and organs. Distributive shock is different from the other three categories of shock in that it occurs even though the output of the heart is at or above a normal level.
Synonymous substitutionA synonymous substitution (often called a silent substitution though they are not always silent) is the evolutionary substitution of one base for another in an exon of a gene coding for a protein, such that the produced amino acid sequence is not modified. This is possible because the genetic code is "degenerate", meaning that some amino acids are coded for by more than one three-base-pair codon; since some of the codons for a given amino acid differ by just one base pair from others coding for the same amino acid, a mutation that replaces the "normal" base by one of the alternatives will result in incorporation of the same amino acid into the growing polypeptide chain when the gene is translated.
HydarthroseA joint effusion is the presence of increased intra-articular fluid. It may affect any joint. Commonly it involves the knee. The approach to diagnosis depends on the joint involved. While aspiration of the joint is considered the gold standard of treatment, this can be difficult for joints such as the hip. Ultrasound may be used both to verify the existence of an effusion and to guide aspiration. File:Knee effusion.jpg|Skyline view of the patella demonstrating a large joint effusion as marked by the arrow.
ProcalcitonineLa procalcitonine (PCT) est une pro-hormone dont le taux sanguin s'élève et peut être mesuré en routine de façon précoce et spécifique lors d'une infection bactérienne mais aussi dans le cas d'infection fongiques ou parasitaires. Cela reste malgré tout un marqueur assez spécifique pour être utilisé en pratique clinique. La procalcitonine est un polypeptide composé de 116 acides aminés (). Il correspond à la pro-hormone de la calcitonine (CT). La PCT est stockée, après sa synthèse, dans des granules de sécrétion dans tous les types cellulaires de l’organisme.
