| 영문 | thyroid gland | 한글 | 갑상샘 |
|---|---|---|---|
| 설명 | 사람의 몸에서 가장 큰 내분비샘으로 목의 앞쪽, 아래쪽에 위치하고 있으며 2엽으로 구성되어 있다. 각 엽은 기관의 양쪽에 있으며 좁은 잘룩에 의해 앞에서 연결되어 있다. 갑상샘호르몬인 티록신(thyroxine)을 분비하고 저장하며, 필요에 따라 방출한다. 또한 갑상샘은 티로칼시토닌(thyrocalcitonin)도 분비한다. 병적인 상태에서 크기가 대개 증가하고, 일부에서는 도리어 위축되며, 통증을 나타내기도 한다. |
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| 영문 | thyroid carcinoma | 한글 | 갑상샘암종 |
|---|---|---|---|
| 설명 | 갑상샘에 생긴 상피세포로 이루어진 악성종양물. 병리조직학적인 형태에 따라 유두상, 소포상, 역형암종 및 수질암종, 림프종 등으로 나눌 수 있다. 다양한 원인이 있으나, 일부에서는 방사선폭로에 의해 발생한다. 치료는 수술, 방사성 옥소, T4 억제요법 등이 사용된다. |
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| 영문 | thyroid hormone | 한글 | 갑상샘호르몬 |
|---|---|---|---|
| 설명 | 광의의 갑상선호르몬은 티록신(thyroxine(T4)), 삼요드티로닌(triiodothyronine (T3)), 티로칼시토닌(thyrocalcitonin)의 3가지중 하나를 말하나 대개의 경우 협의의 뜻으로 사용되며 이 경우 티록신과 삼요드티로닌을 지칭한다. 갑상선 호르몬은 거의 모든 몸세포에서의 바탕질대사에 관여하여 에너지생성을 증가시키고 성장 발육을 촉진한다. 이것은 뇌하수체에서 분비되는 갑상샘 자극호르몬에 의해 합성 및 분비가 촉진된다. 섭취하여 체내에 들어온 요오드가 능동운반에 의해 갑상샘세포내로 들어가 세포내에 있는 단백질인 갑상샘 글로블린과 결합하여 갑상샘호르몬으로 합성된다. 요오드가 3분자 결합한 것을 T3, 4분자 결합한 것을 T4라 부름. 분비되는 갑상선 호르몬중 90%이상이 T4이다. 혈중으로 분비된 갑상샘호르몬은 혈중 단백질과 결합하는데 대부분은 티론신결합글로블린과 결합하며 일부는 알부민과 결합한다. 전반적인 대사율을 촉진시키며 어린이에서는 성장을 촉진시킨다. 특히 어린이에서 몰단백질 합성을 촉진하며 뇌의 발달에 중요한 기능을 함으로써, 선천성 갑상샘저하증(cretinism)을 조기 발견하여 치료하지 못하면 정신지체가 유발된다. 갑상샘과다증의 증상은 체내 대사가 항진되어 식욕이 증가하나 체중이 감소하고 심장박동수가 증가하고 더위를 참지 못하며, 갑상샘기능저하증의 증상은 위와 반대로 식욕이 감소하고 체중이 증가하며 심장박동수가 감소하고 추위를 참지 못하며 피부에 단백질이 축적되어 점액부종이 유발된다. |
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| DE | deprived eye; diagnostic error; dialysis encephalopathy; digestive energy; dose equivalent; dream el... |
|---|---|
| 131I | radioactive Iodine(used in Thyroid uptake, Liver & Kidney Scans & Treatment of malignant & nonmalig... |
| MEN | Multiple Endocrine Neoplasia ; AD Trait 1. MEN Type I(= Wermer Syndro... |
| HTS | head traumatic syndrome; HeLa tumor suppression; human thyroid-stimulating hormone, human thyroid st... |
| TA | alkaline tuberculin; arterial tension; axillary temperature; tactile afferent; Takayasu arteritis; t... |
| CRE | Cyclic AMP responsive elements |
|---|---|
| TRE | thyroid hormone responsive element |
| BEM | Boundary Elements Method |
| CPE | Cytoplasmic polyadenylation elements |
| HSE | Heat Shock Elements |
| antigen-responsive cell | A small lymphocyte that, although not itself an immunologically activated cell, responds to antigenic (immunogenic) stimulus by a process of division and differentiation that results in the production of immunologically activated cells. Synonym: antigen-responsive cell. (05 Mar 2000) |
|---|---|
| chemo-responsive | Responds to chemotherapy, for example, a tumour is chemo-responsive if it shrinks in size following chemotherapy. (16 Dec 1997) |
| sodium-responsive periodic paralysis | A form of periodic paralysis in which the serum potassium level is within normal limits during attacks; onset usually occurs between the ages of 2 and 5 years; there is often severe quadriplegia, usually improved by the administration of sodium salts; autosomal dominant inheritance. Synonym: sodium-responsive periodic paralysis. (05 Mar 2000) |
| DNA-binding protein, cyclic AMP-responsive | A protein that has been shown to function as a calcium regulated transcription factor as well as a substrate for depolarisation-activated calcium calmodulin-dependent protein kinases I and II. This protein functions to integrate both calcium and camp signals. (12 Dec 1998) |
| dopa-responsive dystonia | A condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. Segawa's dystonia is an important variant of DRD. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. Some scientists feel DRD is not only rare but also rarely diagnosed since it mimics many of the symptoms of cerebral palsy. (12 Dec 1998) |
| dystonia, dopa-responsive | A condition successfully treated with drugs. Typically, DRD begins in childhood or adolescence with progressive difficulty in walking and, in some cases, spasticity. Segawa's dystonia is an important variant of DRD. In Segawa's dystonia, the symptoms fluctuate during the day from relative mobility in the morning to increasingly worse disability in the afternoon and evening as well as after exercise. Some scientists feel DRD is not only rare but also rarely diagnosed since it mimics many of the symptoms of cerebral palsy. (12 Dec 1998) |
| familial pyridoxine-responsive anaemia | A rare autosomal recessive hereditary hypochromic anaemia; autosomal trait, responsive to pyridoxine. (05 Mar 2000) |
| actinide elements | Those elements with atomic numbers 89 to 103, corresponding to the lanthanides in the Periodic Table. Synonym: actinide elements. Origin: actinium, first element of the series (05 Mar 2000) |
| alkaline earth elements | Those element's in the family Be, Mg, Ca, Sr, Ba, and Ra, the hydroxides of which are highly ionised and hence alkaline in water solution. (05 Mar 2000) |
| alu elements | <molecular biology> A set of closely related genetic sequences, each about 300 base pairs long, in the human genome. There are 500,000 to 600,000 copies widely dispersed among all 46 chromosomes: They act as markers for human DNA sequences, although their function in the genome is unknown. The DNA fragments containing the Alu elements are formed by digesting genomic DNA with the restriction endonuclease Alu I. (14 Nov 1997) |
| rare earth elements | Those elements with atomic numbers 57-71 which closely resemble one another chemically and were once difficult to separate from one another. Synonym: rare earth elements. Origin: Lanthanum, first element of the series (05 Mar 2000) |
| P elements | A class of transposable elements in Drosophila responsible for hybrid dysgenesis; utilised as tools for introducing genes into new locations in the genome. (05 Mar 2000) |
| copia elements | A mobile genetic element with retrovirus-like sequence organization. (05 Mar 2000) |
| short interspersed elements | Repetitive sequences of DNA of about 300 base pairs in length that occur about every 3000-5000 bp in the genome. (05 Mar 2000) |
| DNA insertion elements | Discrete transposable segments of DNA which can insert into chromosomal, phage, and plasmid DNA. Some insert at random while others are site-specific; most have not been found to exist except in the inserted state. Their insertion into a genome always produces a mutation ("insertion mutation"), and their excision frequently results in a loss of host genetic information. Types of transposable elements include is elements (insertion sequence elements), which are composed of between 700 and 1400 bases and contain no genes unrelated to insertion function and tn elements (transposon elements), which are generally larger than 1400 bases and contain genes unrelated to insertion function. The concept also includes the delta element of saccharomyces cerevisiae and the integration site. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|