| ILP | inadequate luteal phase; insufficiency of luteal phase; interstitial laser photocoagulation; interst... |
|---|---|
| SPIA | solid-phase immunoabsorption; solid-phase immunoassay |
| AI | accidental injury; accidentally incurred; adiposity index; aggregation index; allergy and immunology... |
| AII | acute intestinal infection; second meiotic anaphase |
| M-I | first meiotic metaphase |
| Phase I | phase |
|---|---|
| S phase | synthesis phase |
| APRF | 3/acute phase response factor |
| SPRIA | Solid Phase Radioimmune Assay |
| APR | Acute Phase Response |
| meiotic phase | The stage of nuclear changes in the sexual cells during which reduction of the chromosomes takes place; it embraces the cell generations of the spermatocytes and oocytes. Synonym: reduction phase. (05 Mar 2000) |
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| meiotic | Pertaining to meiosis. (12 Dec 1998) |
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| meiotic division | A specialised form of nuclear division in which there two successive nuclear divisions (meiosis I and II) without any chromosome replication between them. Each division can be divided into 4 phases similar to those of mitosis pro, meta, ana and telophase). Meiosis reduces the starting number of 4n chromosomes in the parent cell to n in each of the 4 daughter cells. Each cell receives only one of each homologous chromosome pair, with the maternal and paternal chromosomes being distributed randomly between the cells. This is vital for the segregation of genes. During the prophase of meiosis I (classically divided into stages: Leptotene, Zygotene, Pachytene, Diplotene and Diakinesis), homologous chromosomes pair to form bivalents, thus allowing crossing over, the physical exchange of chromatid segments. This results in the recombination of genes. Meiosis occurs during the formation of gametes in animals, which are thus haploid and fertilization gives a diploid egg. In plants meiosis leads to the formation of the spore by the sporophyte generation. (18 Nov 1997) |
| meiotic drive | Differential fitness in males and females. (05 Mar 2000) |
| meiotic nondisjunction | Failure of two memberrs of a chromosome pair to separate (disjoin) during meiosis so that both go to one daughter cell and none to the other. This mechanism is responsible for the extra chromosome 21 in trisomy 21 (down syndrome) and for extra and missing chromosomes causing other birth defects and many spontaneous abortions (miscarriages). (12 Dec 1998) |
| meiotic spindle | The meiotic equivalent of the mitotic spindle. (18 Nov 1997) |
| second meiotic division | The second of two consecutive divisions of the nucleus of an eukaryotic cell during the process of meiosis. It includes the following stages of meiosis: prophase II, metaphase II, anaphase II, and telophase II. (09 Oct 1997) |
| first meiotic division | The first of two consecutive divisions of the nucleus of an eukaryotic cell during the process of meiosis. It includes the following stages of meiosis: prophase I, metaphase I, anaphase I, and telophase I. (09 Oct 1997) |
| accelerated phase of leukaemia | Refers to chronic myelogenous leukaemia that is progressing. The number of immature, abnormal white blood cells in the bone marrow and blood is higher than in the chronic phase, but not as high as in the blast phase. (12 Dec 1998) |
| acceleration phase | <cell biology, cell culture> A period of increasing growth before the log phase in a culture of microbes. After the culture is started on a medium, at first there is no growth (the lag phase) and then the microbes start to gradually grow (acceleration phase) until they reach a constant maximum rate of growth (log phase). (15 Jan 1998) |
| acute-phase protein | <haematology> These plasma proteins (in addition to fibrinogen) increase 25% or more in response to inflammation and injury are under direct control of interleukin-6 (IL-6) (hepatocyte-stimulating factor). Other proteins which increase are ceruloplasmin, C3 and C4 which increase 50% or more; alpha-1 acid glycoprotein, alpha-1 antitrypsin, haptoglobin and fibrinogen (the major determinant of viscosity 1 ) which increase two- to fourfold; C-reactive protein (CRP) and serum amyloid A which increase several hundred-fold. Despite long-held clinical opinion to the contrary, available data indicate that neither ESR nor measurement of specific acute-phase reactants are useful in excluding underlying infection or inflammation regardless of the pretest probability. These proteins are secreted into the blood in increased or decreased quantities by hepatocytes in response to trauma, inflammation, or disease. They can serve as inhibitors or mediators of the inflammatory processes. Certain acute-phase proteins have been used to diagnose and follow the course of diseases or as tumour markers. See also: amyloid, c-reactive protein, erythrocyte sedimentation rate, viscosity. (25 Jun 1999) |
| acute-phase reaction | <immunology, rheumatology> Refers to the changes in synthesis of certain proteins within the serum during an inflammatory response, which provides rapid protection for the host against microorganisms via non-specific defense mechanisms. It consists of fever, an increase in inflammatory humoral factors, and an increased synthesis by hepatocytes of a number of proteins or glycoproteins usually found in the plasma; the reaction is mediated by endogenous pyrogens, the hypothalamus, adrenal hormones, and other factors. (12 Jul 2000) |
| anal phase | In psychoanalytic personality theory, the stage of psychosexual development, occurring when a child is between 1 and 3 years, during which activities, interests, and concerns are centreed around the anal zone. (05 Mar 2000) |
| aqueous phase | The water portion of a system consisting of two liquid phase's, one mainly water, the other a liquid immiscible with water (e.g., benzene, ether). (05 Mar 2000) |
| blast phase | Refers to advanced chronic myelogenous leukaemia. In this phase, the number of immature, abnormal white blood cells in the bone marrow and blood is extremely high. Also called blast crisis. (12 Dec 1998) |
| g0 phase | Phase of the cell cycle where cells exist in a quiescent state. These cells have unduplicated DNA, degraded RNA and protein, and low enzyme activity. The ability to switch between g0 and g1 (and vice versa) determines the post-embryonic cell proliferation rate and is defectively controlled in neoplastic cells. (12 Dec 1998) |
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