| 영문 | Golgi body | 한글 | 골지체 |
|---|---|---|---|
| 설명 | 세포내의 세포질 소기관. 골지장치라고도 한다. 1898년 이탈리아의 C. 골지에 의해 올빼미의 신경세포체에서 발견되었으며, 이후 다른 세포에서, 또 근래에는 식물세포에서도 발견되고 있다. 전자 현미경에 의한 연구에서 골지체에 해당되는 부분은 층상구조-꽈리구조-알갱이 구조의 세가지로 되어 있으며, 이것을 골지역이라 한다. 그 작용은 명확하지는 않으나 샘세포의 소포체에서 합성된 분비물이 골지역에서 농축되어 분비과립이 되고, 그 과립의 외측에 막이 형성된다고 생각되고 있다. 골지체는 막구조를 주로 하기 때문에 인지질과 단백질을 많이 가지며 알칼리성 포스파타아제-비타민 C-카로틴 등을 함유한다. |
||
| 영문 | basal body temperature | 한글 | 기초체온 |
|---|---|---|---|
| 설명 | 음식-운동-정신감동 등 체온에 영향을 줄 만한 여러 조건을 피하여 몸과 마음이 안정되었을 때 잰 체온, 보통 아침에 눈을 뜬 직후에 재며, 여성의 경우 월경 주기에 따라 달라지므로 수태 조절이나 자궁, 난소의 병 진단에 응용한다. 6~8시간의 안정된 수면을 취한 후 아침 일찍 깨어나, 잠자리에서 나오기 전에 체온계를 입에 물어서 측정한다. 미묘한 체온의 차이를 측정하는 것이므로 여성체온계를 사용하는 것이 좋다. 이 여성체온계의 수은구부를 혀의 아랫면에 끼우고서 입을 가볍게 다물고 약 5분 동안 있다가 측정하면 된다. 정상적인 기초체온은 복잡한 성주기의 변화를 보이기 때문에 월경주기에 관한 각종 진단을 비롯하여 임신-유산-이상임신의 진단과 수태조절 등에 응용하는 등 여러 가지 효과적인 자료가 된다. |
||
| 영문 | planes of body | 한글 | 인체의 면 |
|---|---|---|---|
| 설명 | 인체를 여러 개로 나누는 면이 있는데, 크게 시상면(sagittal plane), 관상면(coronal plane), 수평면(horizontal plane)으로 나눌 수 있다. 시상면은 인체를 좌우로, 관상면은 앞뒤로, 수평면은 위아래로 가르는 면이다. |
||
| IB | idiopathic blepharospasm; immune body; inclusion body; index of body build; infectious bronchitis; I... |
|---|---|
| LB | lamellar body; large bowel; left breast; left bronchus; left bundle; left buttock; leiomyoblastoma; ... |
| TBS | total body solids; total body solute; total body surface; total burn size; Townes-Brocks syndrome; t... |
| JP drain | The original suction drain. The drain itself is inside the body. It is made of Teflon and has multip... |
| AMA | 1) Anti-Mitochondrial Antibodies 2) American Medical Association |
| AMA | Anti-mitochondrial antibodies |
|---|---|
| AMA | Anti-mitochondrial autoantibodies |
| Mt | Mitochondrial |
| m | Mitochondrial |
| mt DNA | Mitochondrial DNA |
| anti-mitochondrial antibodies | A special serologic test that measures the level of antibodies to a particular portion of a cell (mitochondria). (27 Sep 1997) |
|---|---|
| bovine mitochondrial endonuclease | <enzyme> Dimer of 29kda peptide; prefers a conserved sequence in the displacement loop region of mitochondrial DNA; nicks double-stranded DNA and fragments single-stranded DNA Registry number: EC 3.1.21.- (26 Jun 1999) |
| genome, mitochondrial | The genetic information contained in the circular chromosome of the mitochondrion, a structure located outside the nucleus in the cytoplasm of the cell. The mitochondrial genome and the chromosomal (nuclear) genome together constitute the entire genome. (12 Dec 1998) |
| mitochondrial | Referring to mitochondria. (12 Dec 1998) |
| mitochondrial chromosome | The DNA component of mitochondria, the chief function of which is synthesis of adenosine triphosphate and the management of cellular energy; the chromosome contains some 16,000 base pairs arranged in a circle. The inheritance is matrilineal, and the mutation rate is unusually high; since each cell contains thousands of copies a mutant form may assume an almost continuous gradation as in a galtonian process. Most of the mutations known have their impact on the respiratory chain. (05 Mar 2000) |
| mitochondrial disease | <disease, neurology> An illnesse, frequently neurological, which can be ascribed to defects in mitochondrial function. If the defect is in the mitochondrial rather than the nuclear genome unusual patterns of inheritance can be observed. (18 Nov 1997) |
| mitochondrial encephalomyopathies | Brain diseases associated with disease of the muscles, accompanied by morphological changes in the muscle mitochondria and their metabolism. The mitochondrial encephalopathies are often multisystemic and vary considerably in age at onset, distribution of weakness, severity, and course. Mitochondrial cytochrome c oxidase deficiency appears to be implicated and often several mitochondrial enzymes are affected in the same patient. The brain lesions can be said to be clinical and morphological expressions of a mitochondrial defect. (12 Dec 1998) |
| mitochondrial gene | A functioning gene located not in the nucleus of a cell but in the mitochondrial chromosome. (05 Mar 2000) |
| mitochondrial genome | All of the DNA in the mitochondrial chromosome. (12 Dec 1998) |
| mitochondrial inheritance | The inheritance of a trait encoded in the mitochondrial genome. Because of the oddities of mitochondria, mitochondrial inheritance does not obey the classic rules of genetics. Persons with a mitochondrial disease may be male or female but they are always related in the maternal line and no male with the disease can transmit it to his children. (12 Dec 1998) |
| mitochondrial intermediate peptidase | <enzyme> Removes the octapeptide from the amino terminus of the intermediate protein processed from the protein precursor of certain mitochondrial proteins by the mitochondrial processing peptidase; smip from schizophyllum commune; rmip from rat; ymip from saccharomyces cerevisiae Registry number: EC 3.4.24.59 Synonym: mip peptidase, smip peptidase, rmip peptidase, ymip peptidase (26 Jun 1999) |
| mitochondrial matrix | The substance occupying the space enclosed by the inner membrane of a mitochondrion; it contains enzymes, filaments of DNA, ribosomes, granules, and inclusions of protein crystals, glycogen, and lipid. Synonym: mitochondrial matrix. (05 Mar 2000) |
| mitochondrial membrane | The double biomembrane surrounding the mitochondrion. (05 Mar 2000) |
| mitochondrial myopathies | Diseases of the muscles characterised by morphologic changes in mitochondria and often associated with excessive lipid accumulation. Muscle biopsies reveal "the presence of overly abundant and large mitochondria (often containing abnormal inclusions and cristae) in many muscle fibres. The terms mitochondrial and lipid storage have been used interchangeably to designate these myopathies, since the enzymes essential for intramuscular lipid metabolism are contained in the mitochondria, and a defect in the latter results in an abnormal accumulation of lipid bodies in muscle fibres." often defects in various oxidative enzymes figure. One type of mitochondrial myopathy is called pleoconial with reference to "a remarkably large number (pleo-) of enlarged mitochondria in the biopsied muscle", another is "called megaconial with reference to giant (mega-) mitochondria in the muscle." (adams and victor: principles of neurology, 2d ed, p980-1) (12 Dec 1998) |
| mitochondrial oxidative damage endonuclease | <enzyme> An 8-oxog-specific DNA endonuclease from rat liver mitochondria; recognises and incises at 8-oxog and abasic acid sites in duplex DNA Registry number: EC 3.1.25.- Synonym: oxidative damage-specific endonuclease, mtode enzyme (26 Jun 1999) |
| mitochondrial body |
a fused colony of mitochondria found in the spermatids of insects.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
|
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|