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  • ¿µ¹®
    ÇѱÛ
  • lipoid cell
    ÁöÁú¼¼Æ÷
  • lipoid infarct
    ÁöÁú°æ»ö
  • lipolipoidosis
    Áö¹æÁöÁúÁõ, Áö¹æÀ¯»çÁöÁúÁõ
  • lipolysis
    ÁöÁúºÐÇØ, Áö¹æºÐÇØ
  • lipolytic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • lipolytic necrosis
    Áö¹æ¿ëÇØ±«»ç
  • lipoma
    Áö¹æÁ¾
  • lipomatosis
    Áö¹æÁ¾Áõ
  • lipomatous polyp
    Áö¹æÁ¾Æú¸³
  • lipomelanic reticulosis
    Áö¹æ»ö¼Ò±×¹°Áõ, Áö¹æ»ö¼Ò¸Á»óÁõ
  • lipomeningocele
    Áö¹æ¼ö¸·Å»Ãâ(Áõ), Áö¹æ¼ö¸··ù
  • lipomeria
    ÆÈ´Ù¸®¾øÀ½Áõ, ¼±ÃµÁö°á¼Õ±âÇü
  • lipomyelomeningocele
    Áö¹æÃ´¼ö¼ö¸·Å»Ãâ(Áõ), Áö¹æÃ´¼ö¼ö¸··ù
  • lipopenia
    Áö¹æ°áÇÌ(Áõ)
  • lipophagy
    ÁöÁúÆ÷½Ä, ÁöÁú¿ëÇØ
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  • ¿µ¹®
    ÇѱÛ
  • lipoidal histiocytoma
    (¢¡fibroxanthoma) ¼¶À¯È²»öÁ¾
  • lipoidosis
    (¢¡lipidosis) ÁöÁúÁõ
  • lipolipoidosis
    Áö¹æÁöÁúÁõ
  • lipolysis
    ÁöÁúºÐÇØ, Áö¹æºÐÇØ
  • lipolytic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • lipolytic necrosis
    Áö¹æ¿ëÇØ±«»ç
  • lipoma
    Áö¹æÁ¾
  • lipomatosis
    Áö¹æÁ¾Áõ
  • lipomatous polyp
    Áö¹æÁ¾¼ºÆú¸³
  • lipomelanic reticulosis
    Áö¹æ»ö¼Ò±×¹°Áõ, Áö¹æ»ö¼Ò¼¼¸ÁÁõ
  • lipomeningocele
    Áö¹æ¼ö¸·Å»ÃâÁõ, Áö¹æ¼ö¸··ù
  • lipomeria
    ÆÈ´Ù¸®¾øÀ½Áõ, ¼±ÃµÁö°á¼Õ±âÇü
  • lipomyelomeningocele
    Áö¹æÃ´¼ö¼ö¸··ù, Áö¹æÃ´¼ö¸·Å»ÃâÁõ
  • lipophagy
    ÁöÁú޽Ä, ÁöÁú¿ëÇØ
  • lipopolysaccharide
    ÁöÁú´Ù´çÁú
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  • lipofuscin
    ¸®Æ÷Ǫ½º½Å, Lipofuscin
  • lipofuscin
    Áö¹æ°¥»ö¼Ò,¸®Æ÷Ǫ½º½Å
  • lipofuscin granule
    ¸®Æ÷Ǫ½Å°ú¸³
  • lipogenesis
    Áö¹æ»ý¼º(ò·Û¸ßæà÷).»ýÈ­ÁöÁú»ý¼º.
  • lipogenous
    Áö¹æ»ý¼º(ò·Û¸ßæà÷)ÀÇ.
  • lipogenous diabetes
    Áö¹æ»ý¼º ´ç´¢º´(¡­ÓØèñÜ»).
  • lipohemarthrosis
    Áö¹æ Ç÷°üÀýÁõ(ò·Û¸úìη ï½ñø).
  • lipohistiodiaresis
    Á¶Á÷Áö¹æ°áÇÌ(ðÚòÄò· Û¸ÌÀù¹).
  • lipoic acid
    ¸®Æ÷»ê(¡­ß«).
  • lipoid
    ¸®Æ÷À̵å, À¯ÁöÁú(×¾ò·òõ).
  • lipoid cell
  • lipoid dermatoarthritis
    À¯Áö¹æ ÇǺΠ°üÀý¿°
  • lipoid dermatoarthritis
    ¸®Æ÷À̵åÇǺΰüÀý¿°, À¯ÁöÁúÇǺΰüÀý¿°.
  • lipoid gout
    ¸®Æ÷À̵åÅëdz, À¯ÁöÁúÅëdz.
  • lipoid infarct
    ¸®Æ÷ÀÌµå°æ»ö(¡­ÌÛßá).
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  • ¿µ¹®
    ÇѱÛ
  • lipoylprotein
    ¶óÀÌÆ÷ÀϴܹéÁú(Ó±ÛÜòõ)
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lipocortin <protein> The name given to calcium-binding proteins believed to be secreted by macrophages that acts as an inhibitor of phospholipase A2 enzymes and has a possible role in mediating the antiinflammatry effects of steroids. Lipocortins are identified as proteins of the annexin class and their extracellular role is in some doubt.
(18 Nov 1997)
lipocrit An apparatus and procedure for separating and volumetrically analyzing the amount of lipid in blood or other body fluid.
Origin: Lipo-+ G. Krino, to separate
(05 Mar 2000)
lipocyte Synonym: fat-storing cell.
Origin: Lipo-+ G. Kytos, cell
(05 Mar 2000)
lipodermoid Congenital, yellowish-white, fatty, benign tumour located subconjunctivally.
Origin: Lipo-+ dermoid
(05 Mar 2000)
lipodieresis Synonym: lipolysis.
Origin: Lipo-+ G. Dieresis, division
(05 Mar 2000)
lipodystrophia intestinalis An obsolete term for Whipple's disease.
(05 Mar 2000)
lipodystrophia progessiva superior A condition characterised by a complete loss of the subcutaneous fat of the upper part of the torso, the arms, neck, and face, sometimes with an increase of fat in the tissues about and below the pelvis.
Synonym: Barraquer's disease, lipodystrophia progessiva superior, partial lipoatrophy, Simons' disease.
(05 Mar 2000)
lipodystrophy 1. <biochemistry> Any disturbance of fat metabolism.
2. A group of conditions due to defective metabolism of fat, resulting in the absence of subcutaneous fat, which may be congenital or acquired and partial or total.
Synonym: lipoatrophy, lipodystrophia.
(18 Nov 1997)
lipoedema Oedema of subcutaneous fat, causing painful swellings, especially of the legs in women.
Synonym: cellulite.
(05 Mar 2000)
lipofectin A mixture predominantly of phospholipids used for aiding in the transfer of DNA into cells.
(05 Mar 2000)
lipofection The process of injecting a lipid-complexed or contained DNA into eucaryotic cells.
Origin: Lipo-+ transfection
(05 Mar 2000)
lipoferous Transporting fat.
Origin: Lipo-+ L. Fero, to carry
(05 Mar 2000)
lipofibroma <tumour> A benign neoplasm of fibrous connective tissue, with conspicuous numbers of adipose cells.
(05 Mar 2000)
lipofuscin <protein> Brown pigment characteristic of ageing. Found in lysosomes and is the product of peroxidation of unsaturated fatty acids and symptomatic, perhaps, of membrane damage rather than being deleterious in its own right.
(18 Nov 1997)
lipofuscinosis Abnormal storage of any one of a group of fatty pigments.
Ceroid lipofuscinosis, cerebral sphingolipidosis, late juvenile type.
Neuronal ceroid lipofuscinosis, a group of diseases characterised by accumulation of abnormal pigments in tissue (previously classified as cerebral sphingolipidoses). Major subtypes include chronic juvenile form (Batten disease), slowly progressive behaviour and visual symptoms, autosomal recessive inheritance; acute, late infantile form (Bielschowsky disease); autosomal recessive inheritance; chronic adult form (Kufs disease), variable inheritance; acute infantile form (Santavuori-Haltia disease), fulminating motor and mental deterioration often associated with myoclonic seizures. Minor forms have also been described.
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 3
  • Lipopolysaccharides - »õâ Lipid-containing polysaccharides which are endotoxins and important group-specific antigens. They are often derived from the cell wall of gram-negative bacteria and induce immunoglobulin secretion. The lipopolysaccharide molecule consists of three parts: LIPID A, core polysaccharide, and O-specific chains (O ANTIGENS). When derived from Escherichia coli, lipopolysaccharides serve as polyclonal B-cell mitogens commonly used in laboratory immunology. (From Dorland, 28th ed)
    Synonyms : Lipoglycans
  • Lipoprotein Lipase - »õâ An enzyme of the hydrolase class that catalyzes the reaction of triacylglycerol and water to yield diacylglycerol and a fatty acid anion. The enzyme hydrolyzes triacylglycerols in chylomicrons, very-low-density lipoproteins, low-density lipoproteins, and diacylglycerols. It occurs on capillary endothelial surfaces, especially in mammary, muscle, and adipose tissue. Genetic deficiency of the enzyme causes familial hyperlipoproteinemia Type I. (Dorland, 27th ed) EC 3.1.1.34.
    Synonyms : Diacylglycerol Lipase, Diglyceride Lipase, Post-Heparin Lipase, Postheparin Lipase, Postheparin Lipoprotein Lipase, Factor, Heparin-Clearing, Factor, Lipemia-Clearing, Heparin Clearing Factor, Lipase, Diacylglycerol, Lipase, Diglyceride, Lipase, Lipoprotein
  • Lipoprotein(a) - »õâ A lipoprotein that resembles the LOW-DENSITY LIPOPROTEINS but with an extra protein moiety, APOPROTEIN (A) also known as APOLIPOPROTEIN (A), linked to APOLIPOPROTEIN B-100 on the LDL by one or two disulfide bonds. High plasma level of lipoprotein (a) is associated with increased risk of atherosclerotic cardiovascular disease.
    Synonyms : Lipoprotein (a), Lipoprotein (a-), Lipoprotein Lp(a), Lipoprotein a
  • Lipoprotein-X - »õâ An abnormal lipoprotein present in large amounts in patients with obstructive liver diseases such as INTRAHEPATIC CHOLESTASIS. LP-X derives from the reflux of BILE lipoproteins into the bloodstream. LP-X is a low-density lipoprotein rich in free CHOLESTEROL and PHOSPHOLIPIDS but poor in TRIGLYCERIDES; CHOLESTEROL ESTERS; and protein.
    Synonyms : Lipoprotein X
  • Lipoproteins - »õâ Lipid-protein complexes involved in the transportation and metabolism of lipids in the body. They are spherical particles consisting of a hydrophobic core of TRIGLYCERIDES and CHOLESTEROL ESTERS surrounded by a layer of hydrophilic free CHOLESTEROL; PHOSPHOLIPIDS; and APOLIPOPROTEINS. Lipoproteins are classified by their varying buoyant density and sizes. The large lipoproteins (CHYLOMICRONS; VLDL) are to transport triglycerides, and the small lipoproteins (LDL; HDL) are to transport cholesterol.
    Synonyms : Circulating Lipoproteins, Lipoprotein, Lipoproteins, Circulating
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