| 영문 | smooth muscle | 한글 | 민무늬근육, 평활근육 |
|---|---|---|---|
| 설명 | 근육 중에서 가로무늬가 없는 근. 가로무늬근에 대응되는 말이다. 척추동물에서는 심장근 이외의 내장근은 모두가 민무늬근이다. 많은 내장장기의 벽에 분포되어 있으며, 대개 돌림층과 세로층의 두 층으로 배열되어 있다. 소화관이나 요관 같은 관모양의 구조에서는 꿈틀운동을 일으켜 내용물이 아래로 내려가게 하는 작용을 한다. 항문관, 위, 요도 등에서는 돌림층의 근육이 특히 두꺼워져 내용물이 내려가는 것을 조절하는 조임근육이 형성되어 있다. 혈관에는 돌림층만 있으며, 혈관을 수축하여 혈액을 쥐어짜는 작용을 한다. 또한 자율신경의 지배를 받으며, 우리의 의지와 관계없이 작용한다. |
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| 영문 | voluntary muscle | 한글 | 수의근 |
|---|---|---|---|
| 설명 | 의지의 힘으로 움직일 수 있는 근육. 골격근 외에 피부 내의 피근, 관절주머니에 부착하고 있는 관절근 등이 여기에 속한다. 수의근의 근섬유에는 가로무늬가 있으므로 가로무늬근이라고도 하나, 심장근은 가로 무늬가 있어도 수의근이 아니므로 수의근과 가로무늬근은 동의어는 아니다. 수의근의 운동은 민무늬근보다 빠르다. 수의근이라 해도 골격근 등은 근육무리로서 움직일 수 있으나, 개개의 근육은 따로따로 마음대로 움직이게 할 수 없다. 귓바퀴근육은 사람의 경우 발육이 나빠 마음대로 움직이게 하기 어렵다. |
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| 영문 | facial muscle | 한글 | 얼굴근육 |
|---|---|---|---|
| 설명 | 얼굴의 피부를 움직이고 이에 부착되어 있는 얼굴신경의 공급을 받는 수많은 근육을 포함하는 얼굴표정근이나 모방근. |
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| MS | Maffuci syndrome; maladjustment score; mandibular series; Marfan syndrome; Marie-Strumpell [syndrome... |
|---|---|
| PM | after death (Lat. post mortem); after noon [Lat. post meridiem]; mean pressure; pacemaker; pantomogr... |
| AMI | Acute Myocardial Infarction - Complications(Cx) 1. Early ... |
| ms | muscle |
| SCM | Sterno-Cleido-Mastoid muscle |
| haemoglobin AIc | The major fraction of glycosylated haemoglobin. (05 Mar 2000) |
|---|---|
| haemoglobin Anti-Lepore | A group of abnormal haemoglobins similar to haemoglobin Lepore. These haemoglobins have normal a chains, but the non-a chain consists of the N-terminal portion of the b chain joined to the C-terminal portion of the d chain. This is the opposite crossing over pattern observed in haemoglobin Lepore. Examples of haemoglobin Anti-Lepore include HbMiyada, Hb PCongo, Hb PNilotic, and HbLincoln Park. There is also one variant that is both haemoglobin Lepore and haemoglobin Anti-Lepore (HbParchman). Compare: haemoglobin Lepore. (05 Mar 2000) |
| haemoglobin Bart's | A Hb homotetramer (all four polypeptides identical) of formula g4, found in the early embryo and in alpha-thalassaemia 2; not effective in oxygen transport; does not display a Bohr effect. (05 Mar 2000) |
| haemoglobin C | <haematology> Haemoglobin C is an abnormal version of the protein haemoglobin. The sixth amino acid of the normal beta chain, glutamic acid, is replaced by lysine in haemoglobin C. This mutation causes the red blood cell to be less flexible. (09 Oct 1997) |
| haemoglobin C disease | <haematology> A rare genetic disease of the haemoglobin. Patients are anemic due to the premature breakdown of the blood cells in the spleen. Jaundice may be seen in some patients. There is no specific treatment other than supportive care. (27 Sep 1997) |
| haemoglobin Chesapeake | An abnormal Hb with a single a chain substitution, molecular formula a292Arg→Leub2A; heterozygotes have polycythemia, apparently to compensate for the increased oxygen affinity of this Hb, resulting in decreased liberation of oxygen in the tissues. (05 Mar 2000) |
| haemoglobin Constant Spring | An abnormal haemoglobin having an extended polypeptide chain (31 additional amino acid residues) on the a chain (thus, the a chain is 172 amino acids long); approximately 20% of the individuals with Hb H disease also have this defect. (05 Mar 2000) |
| haemoglobin DPunjab | An abnormal Hb with a single b chain substitution, molecular formula a2Ab2121Glu→ Gln; heterozygotes are asymptomatic, homozygotes have mild haemolytic anaemia; there is an increase in O2 affinity; identical to haemoglobin DLos Angeles, haemoglobin DNorth Carolina, haemoglobin DPortugal, haemoglobin DChicago, and haemoblogin Oak Ridge. (05 Mar 2000) |
| haemoglobin E | <haematology> Haemoglobin E is an abnormal version of the protein haemoglobin, found in Southeast Asia, which plays a role in such medical conditions as microcythaemia, target cell formation, and mild haemolytic anaemia. The beta chain of the haemoglobin is altered because of a mutation. (09 Oct 1997) |
| haemoglobin electrophoresis | <investigation> A special diagnostic procedure which identifies abnormal haemoglobin proteins by the way they migrate in an electric field (electrophoresis). The electric field is used to separate haemoglobin proteins from each other and allow the identification of different components. This can be used to diagnose thalassaemia, sickle cell disease and haemoglobin C disease. (18 Nov 1997) |
| haemoglobin F | <haematology> Haemoglobin f is the normal form of the protein haemoglobin which is found in the foetus. (09 Oct 1997) |
| haemoglobin Gower-1 | A Hb of molecular formula ζ2&vepsilon;2, found as a minor Hb in the early embryo; disappears by the third month of pregnancy in favour of haemoglobin Gower-2 and haemaglobin Portland and then by Hb F; the ζ chain has 141 amino acid residues. Synthesis of the ζ chain is deficient in cases of hydrops foetalis. Compare: haemoglobin Gower-2, haemoglobin Portland. (05 Mar 2000) |
| haemoglobin Gower-2 | A normal Hb of molecular formula a2A&vepsilon;2, which is a major Hb component of the early embryo; production of &vepsilon; chains normally ceases at about the third month of foetal development and is replaced by Hb F. Compare: haemoglobin Gower-1, haemoglobin Portland. (05 Mar 2000) |
| haemoglobin H | <haematology> Haemoglobin H is an abnormal version of the protein haemoglobin. The normal haemoglobin is composed of two alpha and two beta polypeptide chains, haemoglobin H is composed of four beta chains. The molecule has a very high affinity to oxygen, but is very inefficient at transporting it. (09 Oct 1997) |
| haemoglobin I | An abnormal Hb with a single a chain substitution, molecular formula a216Lys→Glub2A; a thalassaemia-like syndrome has been found in individuals heterozygous for both Hb I and alpha-thalassaemia genes, with formation of about 70% Hb I. (05 Mar 2000) |