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"Fanconi Anemia Complementation Group Proteins"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • mountain anemia
    °í»êºóÇ÷
  • macrocytic anemia
    Å«ÀûÇ÷±¸ºóÇ÷, ´ëÀûÇ÷±¸ºóÇ÷
  • megaloblastic anemia
    °Å´ëÀûÇ÷¸ð±¸ºóÇ÷
  • megalocytic anemia
    °Å´ëÀûÇ÷±¸ºóÇ÷
  • microangiopathic hemolytic anemia
    ¹Ì¼¼Ç÷°üº´Áõ¿ëÇ÷ºóÇ÷
  • microcytic anemia
    ÀÛÀºÀûÇ÷±¸ºóÇ÷, ¼ÒÀûÇ÷±¸ºóÇ÷
  • microdrepanocytic anemia
    ÀÛÀº³´ÀûÇ÷±¸ºóÇ÷
  • neonatal anemia
    ½Å»ý¾ÆºóÇ÷
  • normochromic anemia
    Á¤»ó»ö¼ÒºóÇ÷
  • normochromic unresponsive anemia
    ³­Ä¡¼ºÁ¤»ó»ö¼ÒºóÇ÷
  • normocytic anemia
    Á¤»óÀûÇ÷±¸ºóÇ÷
  • normovolemic anemia
    Á¤»óÇ÷·®ºóÇ÷
  • physiological anemia
    »ý¸®ÀûºóÇ÷
  • posthemorrhagic anemia
    ÃâÇ÷ÈĺóÇ÷
  • pernicious anemia
    ¾Ç¼ººóÇ÷
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  • ¿µ¹®
    ÇѱÛ
  • end group
    ¸»´Ü±â
  • end group spine
    ±ê³¡°¡½Ã
  • enteric group
    âÀÚ±Õ±º
  • evocative group therapy
    Ç¥ÇöÁý´Ü¿ä¹ý
  • functional group
    ÀÛ¿ë±â
  • group
    ¹«¸®, ±º, Áý´Ü
  • group-specific
    ±ºÆ¯ÀÌ-
  • glucophore group
    ´ã´ç±â
  • green or yellow vegetable group
    ³ìȲ»öä¼Ò·ù
  • group hospital
    º´¿øÁ¶ÇÕ
  • group medicine
    Áý´ÜÁø·á, Çùµ¿Áø·á
  • group practice
    Áý´Ü°³¾÷
  • group psychotherapy
    Áý´ÜÁ¤½Å¿ä¹ý
  • group displacement law
    Áý´Üº¯À§¹ýÄ¢
  • group fascicular repair
    ½Å°æ¼¶À¯´Ù¹ß±ººÀÇÕ(¹ý)
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  • ¿µ¹®
    ÇѱÛ
  • psittacosis-lymphogranuloma-trachoma (PLT) group
    PLT±º Ŭ¶ó¹Ìµð¾Æ
  • psittacosis-lymphogranuloma-trachoma group
    ¾Þ¹«(»õ)º´ ¸²ÇÁÀ°¾ÆÁ¾Áõ Æ®¶óÄÚ¸¶±º(¡­ë¿ä´ðþñø¡­ÏØ).
  • psittacosis-lymphogranuloma-trachoma group
    ¾Þ¹«(»õ)º´(¡­Ü») ¸²ÇÁÀ°¾ÆÁ¾Áõ Æ®¶óÄÚ¸¶±º(¡­ë¿ä´ðþñø¡­ÏØ)
  • psychotherapy, group
    Áý´ÜÁ¤½ÅÄ¡·á.
  • Cooleys anemia
    Äí¿ï¸®ºóÇ÷.
  • Cooleys anemia
    Äí¿ï¸®ºóÇ÷
  • Cooleys anemia
    Äí¿ï¸®ºóÇ÷.
  • Diamond-Blackfan anemia
    ´ÙÀ̾Ƹóµå-ºí·¢ÆÇ ºóÇ÷
  • Fanconis anemia
    ÆÇÄڴϺóÇ÷
  • Iron deficiency anemia
    ö°áÇ̼ººóÇ÷(ôÑÌÀù¹àõÞ¸úì)
  • Mediterranean anemia
    ÁöÁßÇØºóÇ÷.
  • achlorhydric anemia
    ¹«À§»ê¼º ºóÇ÷(¡­àõÞ¸úì).
  • acute hemolytic anemia
    ±Þ¼º ¿ëÇ÷¼º ºóÇ÷(¡­éÁúìàõÞ¸úì).
  • acute hemolytic anemia
    ±Þ¼º ¿ëÇ÷¼º ºóÇ÷(?ËíÌ´ËÛË×Ì´).
  • acute posthemorrhagic anemia
    ±Þ¼º ÃâÇ÷Èļº ºóÇ÷(¡­õóúìý­àõÞ¸úì).
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  • group practice
    Áý´Ü°³¾÷(̤ËÀ˧ ).
  • group psychotherapy
    Áý´ÜÁ¤½ÅÄ¡·á(ó¢Ó¥ïñãêö½Öû)(¿ä¹ý)
  • group reaction
    Áý´Ü¹ÝÀÀ(̤ËÀËÑËô).
  • group reference value
    Áý´Ü±âÁØ<--ÂüÁ¶>Ä¡
  • group specific C carbohydrate
    ±ºÆ¯ÀÌ C´Ù´çü.
  • group test
    Áý´Ü½ÃÇè(ÊÙËàÌ´).
  • group-specific
    ±ºÆ¯ÀÌÀÇ
  • group-specific C carbohydrate
    ±ºÆ¯ÀÌ C ź¼öÈ­¹°
  • group-specific antigen
    ±º-ƯÀÌÇ׿ø
  • group-specific antigen
    ±ºÆ¯ÀÌÇ׿ø
  • haptenic group
    ÇÕÅÙ±â(¡­Ðñ).
  • hearing aid, group
    Áý´Üº¸Ã»±â
  • high risk group
    °íÀ§Çèµµ±º(Ë­Ëô̴̬˴).
  • hydroxyl group
    ÇÏÀ̵å·Ï½Ç±â(¡­Ðñ).
  • incompatibility group, plasmid
    ÇÃ¶ó½º¹Ìµå ºñÀûÇÕ±º
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  • guanidino group
    ±¸¾Æ´Ïµð³ë±â(Ðñ)
  • guanido group
    ±¸¾Æ´Ïµµ±â(Ðñ)
  • haptenic group
    ÇÕÅÙ±â(Ðñ)
  • high-mobility group
    °íÀ̵¿µµ ±º(ÍÔì¹ÔÑÓøÏØ)
  • hydroxyl group
    ÇÏÀ̵å·Ï½Ç±â(Ðñ)
  • hydroxymethyl group
    ÇÏÀ̵å·Ï½Ã¸ÞÆ¿±â(Ðñ)
  • hypsochromic group
    û»öÀ̵¿±â(ôìßäì¹ÔÑÐñ)
  • imidazole group
    À̴̹ÙÁ¹±â(Ðñ)
  • imino group
    À̹̳ë±â(Ðñ)
  • Inv group
    Inv ±º(ÏØ)
  • ketone group
    ÄÉÅæ±â(Ðñ)
  • labile methyl group
    ºÒ¾ÈÁ¤(ÝÕäÌïÒ)¸ÞÆ¿±â(Ðñ)
  • labile phosphate group
    ºÒ¾ÈÁ¤Àλê±â(ÝÕäÌïÒ×ò߫Ѩ)
  • leaving group
    ÀÌÅ»±â(×î÷­Ðñ)
  • linkage group
    ¿¬°ü±º(Ö¤Î¼ÏØ)
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AIHA Auto-Immune Hemolytic Anemia
AISA Acquired Idiopathic Sideroblastic Anemia
  = RARS
HA   1) Hemolytic Anemia
  2) Head-Ache
IDA   1) Imino-Diacetic Acid
  2) Iron Deficiency Anemia
   &nb...
MAHA Micro-Angiopathic Hemolytic Anemia; PB»ó Helmet Cell
  ThrombocytopeniaÁß MAHAÀ¯¹ß
&nbs...
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CIAV Chicken infectious anemia virus
CDA Congenital dyserythropoietic anemia
EIA Equine Infectious Anemia
EIAV Equine Infectious Anemia Virus
IDA Iron Deficiency Anemia
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 6
contractile proteins Proteins which participate in contractile processes. They include muscle proteins as well as those found in other cells and tissues. In the latter, these proteins participate in localised contractile events in the cytoplasm, in motile activity, and in cell aggregation phenomena.
(12 Dec 1998)
Mx proteins GTPases (70-100 kD) found in interferon treated cells. Mx1 is found in the nucleus and determines the resistance of mice to influenza A virus by blocking transcription of the viral RNA genome. Other Mx proteins are cytoplasmic and are related to dynamin.
(18 Nov 1997)
myc proteins <molecular biology> Family of proteins involved in control of translation, have a C terminal basic helix loop helix zipper domain. Myc Max heterodimers specifically bind the sequence CACGTG with higher affinity than homodimers of either.
(18 Nov 1997)
myelin basic proteins A group of 7 proteins produced from a single gene by alternate splicing found in central and peripheral nervous system myelin. The major basic protein (mbp) has long been of interest because it is the antigen, that, when injected into an animal, elicits a cellular immune response that produces the CNS autoimmune disease called experimental allergic encephalomyelitis (encephalomyelitis, allergic). In the peripheral nervous system, myelin basic protein 18.5 kD is often referred to as the p1 protein.
(12 Dec 1998)
myelin proteins Proteins found in the myelin sheath. The major proteins of central nervous system myelin include: myelin proteolipid protein, myelin basic proteins, and myelin-associated glycoprotein. The major proteins of peripheral nervous system myelin include: myelin basic proteins (myelin p1 protein and myelin p2 protein), myelin p0 protein, and myelin-associated glycoprotein.
(12 Dec 1998)
pregnancy proteins Proteins produced by organs of the mother or the placenta during pregnancy. They may be either pregnancy specific (present only during pregnancy) or pregnancy associated (always present during pregnancy, but may also be present in individuals undergoing oestrogen therapy, taking oral contraceptives or in patients with certain malignancies.)
(12 Dec 1998)
pregnancy zone proteins Glycoproteins with the electrophoretic mobility of an alpha 2-globulin. They are found in small amounts in normal human plasma but in much larger volume in the plasma of pregnant women. These proteins have also been found in increased amounts in individuals undergoing oestrogen therapy and are sometimes produced ectopically by tumours of non-placental origin. Pregnancy zone proteins are believed to be of maternal rather than placental origin.
(12 Dec 1998)
cytoskeletal proteins Major constituent of the cytoskeleton found in the cytoplasm of eukaryotic cells. They form a flexible framework for the cell, provide attachment points for organelles and formed bodies, and make communication between parts of the cell possible.
(12 Dec 1998)
heat-shock proteins 70 <cell biology, protein> A class of molecular chaperones found in both prokaryotes and in several compartments of eukaryotic cells. There is evidence that these proteins can interact with polypeptides during a variety of assembly processes in such a way as to prevent the formation of nonfunctional structures.
(12 Dec 1998)
heat-shock proteins 90 <cell biology, protein> A class of molecular chaperones whose members act in the mechanism of signal transduction by steroid receptors.
(12 Dec 1998)
salivary proteins Proteins found in saliva and the salivary glands. These proteins show some enzymatic activity, but their composition varies in different individuals.
(12 Dec 1998)
helminth proteins Proteins found in any species of helminth.
(12 Dec 1998)
scaffold proteins Proteins that remain when chromosomes are digested with DNase. Many antigenic species have been identified.
(18 Nov 1997)
proteins Nitrogenous organic compounds, containing more than about 100 amino acid residues, molecular weight 8,000-200,000, in vegetable and animal matter. Proteins yield amino acids on hydrolysis and are foods assimilated as amino acids and reconstructed in the protoplasm.
(12 Dec 1998)
proto-oncogene proteins Products of proto-oncogenes. Normally they do not have oncogenic or transforming properties, but are involved in the regulation or differentiation of cell growth. They often have protein kinase activity.
(12 Dec 1998)
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