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Pol polymerase gene
PS1 presenilin 1 gene
Plp proteolipid protein gene
REN renin gene
RYR1 ryanodine receptor gene
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genetic engineering <molecular biology, technique> General term covering the use of various experimental techniques to produce molecules of DNA containing new genes or novel combinations of genes, usually for insertion into a host cell for cloning.
(07 May 1998)
genetic engineering technologies See: recombinant DNAtechnologies.
(09 Oct 1997)
genetic equilibrium A condition in which the rate of an allele's forward mutation is cancelled out by its rate of reverse mutation.
(09 Oct 1997)
genetic female An individual with a normal female karyotype, including two X chromosomes, an individual whose cell nuclei contain Barr sex chromatin bodies, which are normally absent in males.
(05 Mar 2000)
genetic fine structure The study of genes on the level of their nucleotide sequences and what happens to their molecular structure at that level.
(09 Oct 1997)
genetic fingerprint 1. An impression of the inked bulb of the distal phalanx of a finger, showing the configuration of the surface ridges, used as a means of identification.
See: dermatoglyphics, Galton's system of classification of fingerprints.
2. Term, sometimes used informally, referring to any analytical method capable of making fine distinctions between similar compounds or gel patterns; e.g., the pattern of an infrared absorption curve or of a two-dimensional paper chromatograph.
3. In genetics, the analysis of DNA fragments to determine the identity of an individual or the paternity of a child.
Synonym: genetic fingerprint.
(05 Mar 2000)
genetic fingerprinting The process of comparing the nucleotide sequences of different DNA samples to find out if the samples are from the same individual or not. This is often used as a way to investigate crime, for example by comparing samples found at the crime scene with samples from the suspects.
(09 Oct 1997)
genetic fitness In a phenotype, the mean number of surviving offspring that it generates in its lifetime, usually expressed as a fraction or percentage of the average genetic fitness of the population.
(05 Mar 2000)
genetic fixation The increase of the frequency of a gene by genetic drift until no other allele is preserved in a specific finite population.
(05 Mar 2000)
genetic heterogeneity The presence of apparently similar characters for which the genetic evidence indicates that different genes or different genetic mechanisms are involved in different pedigrees. In clinical settings genetic heterogeneity refers to the presence of a variety of genetic defects which cause the same disease, often due to mutations at different loci on the same gene, a finding common to many human diseases including alzheimer's disease, cystic fibrosis, lipoprotein lipase and polycystic kidney disease.
(12 Dec 1998)
genetic homeostasis The tendency of a population to reach a point of genetic equilibrium and resist changes.
Origin: Gr. Stasis = stoppage
(09 Oct 1997)
genetic human male An individual with a karyotype containing a Y chromosome, an individual whose cell nuclei do not contain Barr sex chromatin bodies, which are normally present in females. Patients with ambiguous sexual development and those with Turner's syndrome are classed as genetic male's or genetic females according to the absence or presence of Barr bodies even though their sex chromosome complement may suggest otherwise.
(05 Mar 2000)
genetic identity The relatedness of two populations as represented by the percentage of the genes they share.
(09 Oct 1997)
genetic induction The triggering of a specific gene by an inducer molecule (which acts directly or indirectly by affecting an RNA polymerase molecule).
(09 Oct 1997)
genetic information The heritable biological information coded in the nucleotide sequences of DNA or RNA (certain viruses), such as in the chromosomes or in plasmids.
(09 Oct 1997)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 18
  • Genes, Immunoglobulin Heavy Chain - »õâ Genes and gene segments encoding the IMMUNOGLOBULIN HEAVY CHAINS. Gene segments of the heavy chain genes are symbolized V (variable), D (diversity), J (joining), and C (constant).
    Synonyms : Immunoglobulin VH Germ Line Genes
  • Genes, Immunoglobulin Light Chain - »õâ Genes and gene segments encoding the IMMUNOGLOBULIN LIGHT CHAINS. Gene segments of the light chain genes are designated as V (variable), J (joining), and C (constant).
    Synonyms : Immunoglobulin Light Chain Genes
  • Genes, Insect - »õâ The functional hereditary units of INSECTS.
    Synonyms : Gene, Insect, Insect Gene
  • Genes, Intracisternal A-Particle - »õâ Genes of IAP elements (a family of retrovirus-like genetic elements) which code for virus-like particles (IAPs) found regularly in rodent early embryos. ("Intracisternal" refers to the cisternae of the endoplasmic reticulum.) Under certain circumstances, such as DNA hypomethylation they are transcribed. Their transcripts are found in a variety of neoplasms, including plasmacytomas, neuroblastoma, rhabdomyosarcomas, teratocarcinomas, and colon carcinomas.
    Synonyms : Gene, Intracisternal A Particle, A-Particle Element, Intracisternal, A-Particle Elements, Intracisternal, A-Particle Gene, Intracisternal, A-Particle Genes, Intracisternal, Element, IAP, Element, Intracisternal A-Particle, Elements, IAP, IAP Element
  • Genes, jun - »õâ Retrovirus-associated DNA sequences (jun) originally isolated from the avian sarcoma virus 17 (ASV 17). The proto-oncogene jun (c-jun) codes for a nuclear protein which is involved in growth-related transcriptional control. Insertion of c-jun into ASV-17 or the constitutive expression of the c-jun protein produces tumorgenicity. The human c-jun gene is located at 1p31-32 on the short arm of chromosome 1.
    Synonyms : c-jun Proto-Oncogenes, jun Oncogene, jun Proto-Oncogene, v-jun Oncogenes, Oncogene, jun, Oncogenes, jun, Proto-Oncogene, jun, Proto-Oncogenes, jun, c jun Genes, c jun Proto Oncogenes, c-jun Gene, c-jun Proto-Oncogene, jun Gene, jun Oncogenes, jun Proto Oncogene
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genetic counseling A counseling process for those with either a family history of a genetic disorder or those who are at risk for having a child with a genetic disease.
Ãâó: www.ehealthmd.com/library/amniocentesis/AMO_glossa...
generation time The time interval between successive cell divisions.
Ãâó: www.genpromag.com/Glossary~LETTER~G.html
genetic code The code by which a nucleotide sequence is translated into an amino acid sequence. Each three nucleotide triplet constitutes a codon; the 64 codons correspond to 20 amino acids and to signals for the initiation and termination of transcription.
Ãâó: www.genpromag.com/Glossary~LETTER~G.html
genetic drift A change of gene frequencies within a population over time.
Ãâó: www.genpromag.com/Glossary~LETTER~G.html
genetic map A map of relative chromosomal locations based on recombination data.
Ãâó: www.genpromag.com/Glossary~LETTER~G.html
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