| MCC | mean corpuscular hemoglobin concentration; medial cell column; Medical Council of Canada; metacerebr... |
|---|---|
| MSSG | multiple sclerosis susceptibility gene |
| PAG | periaqueductal gray [matter]; polyacrylamide gel; pregnancy-associated globulin; proliferation-assoc... |
| PAGA | proliferation-associated gene A |
| PHOX | paired mesoderm homeobox [gene] |
| gene regulation | The DNA and protein interactions in a gene that determine the temporal and spatial modes of expression as well as the amplitude of expression. (14 Nov 1997) |
|---|---|
| gene regulatory protein | <molecular biology> Any protein that interacts with DNA sequences of a gene and controls its transcription. (18 Nov 1997) |
| gene sequencing | Determination of the sequence of nucleotide bases in a strand of DNA. (14 Nov 1997) |
| gene splicing | A procedure by which one DNA molecule or fragment can be attached to another. (14 Nov 1997) |
| gene supression | <molecular biology> The halting of abnormal gene activity which results in the restoration of lost or impaired genetic function. (09 Oct 1997) |
| mapping, gene | Charting the positions of genes on chromosome and learning the distance, in linkage units or physical units, between genes. (12 Dec 1998) |
| gene switch | <molecular biology> A situation in which a cell or organism stops expressing one gene orgene group and switches to expressing a different gene or group of genes. (09 Oct 1997) |
| gene synthesis | <molecular biology> The complete synthesis of a gene using a DNA synthesiser (gene machine), or the assembly of oligonucleotides so synthesised into a synthetic gene, as opposed to cloning. (14 Nov 1997) |
| gene targeting | The integration of exogenous DNA into the genome of an organism at sites where its expression can be suitably controlled. This integration occurs as a result of homologous recombination. (12 Dec 1998) |
| gene testing | Testing a sample of blood (or another fluid or tissue) for evidence of a gene. The evidence can be biochemical, chromosomal, or genetic. The aim is to learn whether a gene for a disease is present or absent. (12 Dec 1998) |
| gene therapy | <molecular biology> Treatment of a disease caused by malfunction of a gene, by stably transfecting the cells of the organism with the normal gene. (18 Nov 1997) |
| gene transfer | <molecular biology> General tem for the insertion of foreign genes into a cell or organism. Synonymous with transfection. (18 Nov 1997) |
| gene translocation | The movement of a gene fragment from one chromosomal location to another, which often alters or abolishes expression. (09 Oct 1997) |
| receptors, calcitonin gene-related peptide | Cell surface proteins that bind calcitonin gene-related peptide (cgrp) with high affinity and trigger intracellular changes which influence the behaviour of cells. Cgrp receptors are present in both the central nervous system and the periphery and are not the same as calcitonin receptors. (12 Dec 1998) |
| recessive gene | A gene that is expressed onlywhen it is present in two copies or if theother copy is missing. (09 Oct 1997) |