| 영문 | Papanicolaou smear(test) | 한글 | 파파니콜로 도말검사 |
|---|---|---|---|
| 설명 | 줄여서 팝도말검사(Pap smear)이라고 부른다. 여성의 자궁목암의 발생을 미리 알아보기 위해 시행하는 검사법으로 미국에서는 이 방법으로 현재 자궁목암발생에 의한 사망률을 현저히 낮추고 있다. 방법은 산부인과에서 시행하며, 여성의 자궁목에서 세포를 가져다가 도말하여 현미경으로 검사한다. 요즈음에 와서는 자궁목뿐 아니라 호흡기나 비뇨기 등 분비물을 도말하여 파파니콜로 염색을 하여 검사하는 것도 여기에 포함된다. (그림 P-3). |
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| 영문 | glucose tolerance test | 한글 | 포도당견딤검사 |
|---|---|---|---|
| 설명 | 포도당견딤 검사란 당뇨병의 진단에 사용되는 검사로 당을 체내에 투여하고 시간 별로 혈액을 채취하여 혈당의 농도를 재어서 고혈당 여부를 조사하는 검사이다. 주로 경구포도당견딤검사(oral glucose tolerance test)를 많이 하는데 이것은 10~16시간의 금식 후에 채혈을 한번 한뒤에 도당 75g을 250~300mL의 물에 녹여 5분에 걸쳐서 마시게 하고 매시간 별로 채혈을 하여 혈당의 농도를 첵크한다. 공복시에 정맥에서 채혈하여 측정한 혈당이 140mg/dL이상이거나 포도당견딤 검사 2시간후의 혈당이 200mg/dL이상일 경우에는 당뇨병으로 진단을 한다. 그러나 이 검사를 실시할 경우에 주의해야 할 점은 검사전 3일간 하루에 150g이상의 탄수화물을 섭취해야 한다는 것과 검사도중에 운동, 흡연 등을 하지 않아야 한다는 것이다. |
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| 영문 | blood test | 한글 | 혈액검사 |
|---|---|---|---|
| 설명 | 혈액형이나 질병 유무 따위를 알기 위하여 피를 뽑아 행하는 검사. 몸 전체의 장기나 조직에 병터가 있으면 이들 성분에 변화가 있게 되어 진단에 큰 도움을 준다. |
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| TOFHLA | test of functional health literacy in adults |
|---|---|
| PS test | Pancreozymin-Secretion test = combined secretin-CCK test |
| AAT | Aachen Aphasia Test; academic aptitude test; alanine aminotransferase; alkylating agent therapy; alp... |
| AST | allergy serum transfer; angiotensin sensitivity test; anterior spinothalamic tract; antistreptolysin... |
| CPT | carnitine palmityl transferase; carotid pulse tracing; chest physiotherapy; child protection team; c... |
| BRCA1 breast cancer susceptibility gene | This mutated (changed) version of the BRCA1 gene makes a person susceptible to developing breast cancer. (12 Dec 1998) |
|---|---|
| calcitonin gene-related peptide | <protein> A second product transcribed from the calcitonin gene. Calcitonin gene related peptide is found in a number of tissues including nervous tissue. It is a vasodilator that may participate in the cutaneous triple response. It is a neuropeptide of 37 amino acids with structural homology to salmon calcitonin. Co-localises with substance P in neurons. It occurs as a result of alternative processing of mRNA from the calcitonin gene. The neuropeptide is widely distributed in neural tissue of the brain, gut, perivascular nerves, and other tissue. The peptide produces multiple biological effects and has both circulatory and neurotransmitter modes of action. In particular, it is a potent endogenous vasodilator. Intracerebral administration leads to a rise in noradrenergic sympathetic outflow, a rise in blood pressure and a fall in gastric secretion. Acronym: CGRP (05 May 2002) |
| cancer susceptibility gene | tumour suppressor gene |
| rab gene | 1. <molecular biology> One of the three main groups of ras like genes specifying small GTP-binding proteins (the others are ras and rho). Rab proteins are involved in vesicular traffic and seem to control translocation from donor to acceptor membranes. 2. <cell biology> Gene family in plants responsive to abscisic acid: encode proteins of 15-17 kD. (18 Nov 1997) |
| pair rule gene | <molecular biology> A segmentation gene, expressed sequentially between gap genes and segment polarity genes. In development of Drosophila, a set of about 8 genes that are expressed only in alternate segments (odd or even) of the developing embryo. Loss of function mutants thus lack alternate segments. Examples: even skipped (eve), fushi tarazu (ftz), hairy. (18 Nov 1997) |
| variable gene | <molecular biology> Those regions in the amino acid sequence of both the heavy and the light chains of immunoglobulins where there is considerable sequence variability from one immunoglobulin to other of the same class, in contrast to constant sequence (C) regions. The V regions are associated with the antigen binding areas. They contain hypervariable regions of particularly high sequence diversity. (18 Nov 1997) |
| gap gene | <molecular biology> Segmentation genes involved in specifying relatively coarse subdivisions of the embryo. They are expressed sequentially in development between egg polarity genes and pair rule genes. In Drosophila, there are at least three such genes, for example Kruppel. (18 Nov 1997) |
| gene | <cell biology, molecular biology> Originally defined as the physical unit of heredity, it is probably best defined as the unit of inheritance that occupies a specific locus on a chromosome, the existence of which can be confirmed by the occurrence of different allelic forms. Genes are formed from DNA, carried on the chromosomes and are responsible for the inherited characteristics that distinguish one individual from another. Each human individual has an estimated 100,000 separate genes. Given the occurrence of split genes, it might be redefined as the set of DNA sequences (exons) that are required to produce a single polypeptide. (09 Oct 1997) |
| gene activation | The process of activation of a gene so that it is expressed at a particular time. This process is crucial in growth and development. (05 Mar 2000) |
| gene amplification | <molecular biology> Selective replication of DNA sequence within a cell, producing multiple extra copies of that sequence. The best known example occurs during the maturation of the oocyte of Xenopus, where the set (normally 500 copies) of ribosomal RNA genes is replicated some 4,000 times to give about 2 million copies. (18 Nov 1997) |
| gene bank | A group of genes which are coordinately controlled. (09 Oct 1997) |
| gene cloning | <molecular biology> The insertion of a DNA sequence into a vector that can then be propagated in a host organism, generating a large number of copies of the sequence. (18 Nov 1997) |
| gene cluster | A set of closely related genes that code for the same or similar proteins and which are usuallygrouped together on the same chromosome. (09 Oct 1997) |
| gene conversion | <molecular biology> A phenomenon in which alleles are segregated in a 3:1 not 2:2 ratio in meiosis. May be a result of DNA polymerase switching templates and copying from the other homologous sequence or a result of mismatch repair (nucleotides being removed from one strand and replaced by repair synthesis using the other strand as template). (18 Nov 1997) |
| gene deletion | The total loss (or absence) of a gene. Gene deletion plays a role in birth defects and in the development of cancer. (12 Dec 1998) |