| 영문 | mucinous tumor | 한글 | 점액종양 |
|---|---|---|---|
| 설명 | 점액으로 구성된 종양을 말하는데 주로 여성의 난소에서 발생하는 낭성(물주머니같은 종양을 말함) 종양에서 많이 볼 수 있다. |
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| 영문 | tumor | 한글 | 종양 |
|---|---|---|---|
| 설명 | 조절할 수 없이 계속 진행되는 세포분열에 의한 조직의 새로운 증식 및 증대. 신생물. (1) 분류 A. 침윤과 전이의 유무에 따라 i)양성종양: 침윤과 전이가 없고 역형성이 낮은 세포로 구성됨. 대개 치료에 반응이 높고, 생명에 크게 지장이 없으며, 재발하는 경우도 적다. 증상은 단지 주위조직에 대한 압박정도이다. ii)악성종양: 침윤과 전이가 있고 퇴화도가 높은 세포로 구성됨. 기원세포가 상피조직일 경우 암종, 비상피성일 경우 육종으로 나누기도 한다. 치료에 잘 반응하지 않고, 재발을 잘 하며, 생존율이 낮다. 흔히 말하는 “암”을 의미한다. B. 조직학적 특징에 따라 샘종, 지방종, 근종 등으로 나누기도 한다. (2) 병리조직학적 특징 A. 육안적 소견 덩어리를 형성하기도 하고 정상조직에 스며들듯이 판상구조를 이루기도 하는 등 다양한 형태를 보인다. 양성의 경우 피막을 가진 경우가 많고 악성의 경우 없는 경우가 많다. 육안소견에 따라 다음과 같이 나눈다. 낭성, 융기성, 괴사성, 폴립모양, 궤양형 등이 있다. 또는 세포의 크기와 모양이 비정상적인 형태로 변화한다. 핵의 극성이 사라지고 핵의 염색성이 짙어진다. 세포질의 염색성도 변화하며 세포들간의 세포주기가 매우 다양해져 많은 세포분열을 보인다. 이러한 일련의 변화를 역형성이라 한다. 역형성의 정도에 따라 조직학적 등급을 나눈다. 또한 각 종양에 따라 각기 다른 병리조직학적 명칭을 붙인다. |
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| SAI | Self-Analysis Inventory; Sexual Arousability Inventory; Social Adequacy Index; suppressor of anchora... |
|---|---|
| SCA | self-care agency; severe congenital anomaly; sickle-cell anemia; single-camera autostereoscopic [ima... |
| SF | Sabin-Feldman [test]; safety factor; salt-free; scarlet fever; screen film; seminal fluid; serosal f... |
| SIRS | soluble immune response suppressor; Structured Interview of Reported Symptoms; systemic inflammatory... |
| SSCA | spontaneous suppressor cell activity |
| 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) |
| gene disorder | Hereditary disorder caused by a mutant allele of a single gene (e.g., Duchenne muscular dystrophy, retinoblastoma, sickle cell disease). Compare polygenic disorders. (05 Mar 2000) |
| gene disruption | Use of both in vitro and in vivo recombination to substitute an easily selected mutant gene for a wild-type gene. (09 Oct 1997) |
| gene divergence | The difference (expressed as a percentage) in the nucleotide sequencesbetween two related genes that developed from the same ancestral gene. (09 Oct 1997) |
| gene dosage | <molecular biology> Number of copies of a particular gene locus in the genome, in most cases either one or two. (18 Nov 1997) |
| tumor suppressor gene |
Genes that normally restrain cell growth but, when missing or inactivated by mutation, allow cells to grow uncontrolled. The P53 gene is an example.
출처: www.nexxusscotland.com/media_centre/glossary.html
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