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  • ¿µ¹®
    ÇѱÛ
  • ectopic hormone
    µý°÷È£¸£¸ó, À̼ҼºÈ£¸£¸ó
  • estrogenic hormone
    ¿¡½ºÆ®·Î°Õ
  • female hormone
    ¿©¼ºÈ£¸£¸ó
  • follicle stimulating hormone
    ³­Æ÷ÀÚ±ØÈ£¸£¸ó
  • gonadotropic hormone
    »ý½Ä»ùÀÚ±ØÈ£¸£¸ó, »ý½Ä¼±ÀÚ±ØÈ£¸£¸ó
  • gonadotropin-releasing hormone
    »ý½Ä»ùÀÚ±ØÈ£¸£¸óºÐºñÈ£¸£¸ó, »ý½Ä¼±ÀÚ±ØÈ£¸£¸óºÐºñÈ£¸£¸ó
  • gonadotropin-releasing hormone agonist
    »ý½Ä»ùÀÚ±ØÈ£¸£¸ó¹æÃâÈ£¸£¸óÀÛ¿ëÁ¦
  • growth hormone
    ¼ºÀåÈ£¸£¸ó
  • hypophysiotropic hormone
    ³úÇϼöüÀÚ±ØÈ£¸£¸ó
  • hypothalamic inhibitory hormone
    ½Ã»óÇϺξïÁ¦È£¸£¸ó
  • hypothalamic releasing hormone
    ½Ã»óÇϺκкñÈ£¸£¸ó
  • hormone
    È£¸£¸ó
  • hormone bombardment
    È£¸£¸óÃæ°Ý¿ä¹ý
  • hormone dependent
    È£¸£¸óÀÇÁ¸-
  • hormone replacement therapy
    È£¸£¸ó´ëġġ·á
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  • ¿µ¹®
    ÇѱÛ
  • type strain
    Ç¥ÁرÕÁÖ
  • type
    Çü, À¯Çü
  • test type
    ½Ã°¢Ç¥, ½ÃÇ¥
  • adrenal corticotropic hormone
    ºÎ½Å°ÑÁúÀÚ±ØÈ£¸£¸ó
  • adrenocortical hormone
    ºÎ½Å°ÑÁúÈ£¸£¸ó
  • adrenocorticotropic hormone
    ºÎ½Å°ÑÁúÀÚ±ØÈ£¸£¸ó
  • adrenomedullary hormone
    ºÎ½Å¼ÓÁúÈ£¸£¸ó
  • androgenic hormone
    ³²¼ºÈ£¸£¸ó
  • antidiuretic hormone
    Ç×ÀÌ´¢È£¸£¸ó
  • hormone bombardment
    È£¸£¸óÃæ°Ý¿ä¹ý
  • corticosteroid hormone
    ÄÚ¸£Æ¼ÄÚ½ºÅ×·ÎÀ̵åÈ£¸£¸ó
  • corticotropin-releasing hormone
    ÄÚ¸£Æ¼ÄÚÆ®·ÎÇɺкñÈ£¸£¸ó
  • diabetogenic hormone
    ´ç´¢º´¹ß»ýÈ£¸£¸ó
  • digestive hormone
    ¼ÒÈ­È£¸£¸ó
  • hormone dependent
    È£¸£¸óÀÇÁ¸
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  • ¿µ¹®
    ÇѱÛ
  • receptor site
    ¼ö¿ëüºÎÀ§.
  • receptor stimulants
    ¼ö¿ëüÀÚ±ØÁ¦.
  • receptor supersensitivity
    ¼ö¿ëü Ãʰ¨¼ö¼º(áôéÄô÷ õ±Êïáôàõ)
  • receptor, T cell
    T¼¼Æ÷(Ç׿ø)¼ö¿ëü
  • receptor-ligand interaction
    ¼ö¿ëü-¹èÀ§ÀÚ »óÈ£ÀÛ¿ë
  • B type virus particle
    BÇü ¹ÙÀÌ·¯½ºÀÔÀÚ.
  • B type virus particle
    BÇü ¹ÙÀÌ·¯½ºÀÔÀÚ.
  • C type particle
    CÇüÀÔÀÚ
  • C-type particle
    CÇü ÀÔÀÚ (·¹Æ®·Î¹ÙÀÌ·¯½ºÀÇ)
  • C-type virus particle
    CÇü ¹ÙÀÌ·¯½ºÀÔÀÚ.
  • Charcot-Marie type
    »þ¸£ÄÚ-¸¶¸®Çü.
  • Duchenne-Landouzy type
    µÚ½Ã¿£´À-¶õµÎ¿ìÁöÇü.
  • Gougerot-Ruiter type vasculitis
    ±¸Á¦·Î ·çÀÌÅÍ Çü Ç÷°ü¿°
  • L-type chnnels
    L-Çü Åë·Î(÷×ÖØ)
  • Lafora body type of myoclonus
    ¶óÆ÷¶ó üÇü ¸¶ÀÌ¿ÀŬ·Î´©½º.
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  • ¿µ¹®
    ÇѱÛ
  • complement receptor 1
    º¸Ã¼ ¼ö¿ëü 1
  • complement receptor 2
    º¸Ã¼¼ö¿ëü 2
  • complement receptor 3
    º¸Ã¼¼ö¿ëü 3
  • complement receptor 4
    º¸Ã¼¼ö¿ëü 4
  • corpuscular receptor
    ¼Òü ¼ö¿ëü
  • distance receptor
    °Å¸®¼ö¿ë±â.
  • distance receptor
    °Å¸®(Ëå×î)¼ö¿ë±â(áôé»Ðï).
  • dominant receptor
    ¿ì¼º¼ö¿ëü.
  • dominant receptor
    ¿ì¼º¼ö¿ëü(éÐàõáôé»ô÷).
  • dopamine receptor
    µµÆÄ¹Î ¼ö¿ëü
  • dopamine receptor
    µµÆÄ¹Î ¼ö¿ëü(áôé»ô÷)
  • dopamine receptor antagonist
    µµÆÄ¹Î ¼ö¿ëü ±æÇ×Á¦
  • drug receptor
    ¾à¹°¼ö¿ëü.
  • drug receptor
    ¾à¹°¼ö¿ëü(å·Úªáôé»ô÷).
  • early receptor potential
    Á¶±â½Ã¼¼Æ÷ÀüÀ§
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  • ¿µ¹®
    ÇѱÛ
  • receptor
    ¼ö¿ëü(áôé»ô÷)
  • receptor destroying enzyme
    ¼ö¿ëü ÆÄ±«È¿¼Ò(áôé»ô÷÷òÎÕý£áÈ)
  • receptor down regulation
    ¼ö¿ëü ÇÏÇâ Á¶Àý(áôé»ô÷ù»ú¾ðàï½)
  • receptor element
    ¼ö¿ëü Á¶Àý ¿ä¼Ò(áôé»ô÷ðàï½é©áÈ)
  • receptor gradient
    ¼ö¿ëü ±¸¹è(áôé»ô÷ÎþÛÕ)
  • receptor internalization
    ¼ö¿ëü ³»ÀÔ(áôé»ô÷Ò®ìý)
  • receptor-mediated endocytosis
    ¼ö¿ëü¸Å°³ ¼¼Æ÷³» ÀÌÀÔ(áôé»ô÷ØÚË¿á¬øàÒ®ì¹ìý)
  • ribosome receptor
    ¶óÀ̺¸¼Ø ¼ö¿ëü(áôé»ô÷)
  • spare receptor
    ¿¹ºñ(çãÝá) ¼ö¿ëü (â¥é»ô÷)
  • SRP receptor
    SRP ¼ö¿ëü(áôé»ô÷)
  • steroid receptor
    ½ºÅ×·ÎÀÌµå ¼ö¿ëü (áôé»ô÷)
  • virus receptor
    ¹ÙÀÌ·¯½º ¼ö¿ëü (â¥é»ô÷)
  • volume receptor
    ¿ëÀû ¼ö¿ë±â(é»îÝáôé»Ðï)
  • adipokinetic hormone
    Áö¹æµ¿¿ø(ò·Û²ÔÑê¬)È£¸£¸ó
  • adrenal cortical hormone
    ºÎ½ÅÇÇÁú(Üùãìù«òõ)È£¸£¸ó
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LHRH Luteinizing Hormone Releasing Hormone
  ? GnRH; Gonadotropin Releasing Hormone
&nbs...
FSH/LR-RH follicle-stimulating hormone and luteinizing hormone releasing hormone
NF Neuro-Fibromatosis
  = Von Recklinghausen's Disease
  NF 1; Neuro-Fibroma...
PFKL phosphofructokinase, liver type; 6-phosphofructo-2-kinase, liver type
PFKP phosphofructokinase, platelet type; 6-phosphofructo-2-kinase, platelet type
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 5
GH-RIH Growth hormone release inhibiting hormone
GRH Growth hormone-releasing hormone
hGHRH Human growth-hormone-releasing hormone
LH-RH Luteinising Hormone-Releasing Hormone
LRH Luteinizing Hormone Releasing Hormone
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • melanophorotropic hormone
    ¸á¶ó³ëÆ÷¸£ ģȭ¼º È£¸£¸ó
  • molting hormone
    Å»ÇÇ È£¸£¸ó
  • multiple somatic receptor
    ´Ù¹ß¼º ü ¼ö¿ëü, ´Ù¹ß¼º ü ¼ö¿ë±â
  • N-hormone
    N-È£¸£¸ó
    ºÎ½Å ÇÇÁú ³»ºÐºñ È£¸£¸óÀÇ Çϳª.
  • natriuretic hormone
    ³ªÆ®·ý ¹è¼³ Áõ°¡ È£¸£¸ó, ³ªÆ®·ý ¹è¼³ ÃËÁø È£¸£¸ó
  • opiate analgesia receptor
    ¾ÆÆí¼º ÁøÅë ¼ö¿ëü, ¾ÆÆí¼º ÁøÅë ¼ö¿ë±â
  • opiate receptor
    ¾ÆÆí ¼ö¿ëü, ¾ÆÆí ¼ö¿ë±â
    1. ¥ì : ¥ì1Àº µ¿Åë Á¶Àý ¾àÁ¦°¡ °áÇÕ, ¥ì2¿Í °áÇսô ȣÈíÀÌ ¾ïÁ¦µÈ´Ù. 2. ¥ê¿Í °áÇÕ ½Ã Â÷ºÐÇØÁø´Ù. 3. ¥ä : ¸ö¿¡¼­ »ý¼ºµÇ´Â ³»Àμº o
  • pancreatic hormone
    ÃéÀå È£¸£¸ó
  • peptide hormone
    ÆéƼµå È£¸£¸ó
  • peripheral receptor
    ¸»ÃÊ ¼ö¿ëü, ¸»ÃÊ ¼ö¿ë±â
  • placental hormone
    Źݼº È£¸£¸ó, ÅÂ¹Ý È£¸£¸ó
    Æ÷À¯·ùÀÇ Å¹ݿ¡¼­ ºÐºñµÇ´Â È£¸£¸ó. »ç¶÷, ¿ø¼þÀÌ µî¿¡¼­ º¼ ¼ö ÀÖ´Â »ý½Ä¼± ÀÚ±Ø È£¸£¸óÀÇ ºÐºñ¶ó°í ÁÖÀåÇÏ´Â ÇÐÀÚµµ ÀÖ´Ù. ´Ù¸¸ À̵é È£¸£¸óÀÇ ÀÛ¿ëÀº ³úÇϼöü Àü¿±ÀÇ »ý½Ä¼± ÀÚ±Ø È£¸£¸ó°ú´Â »ý¸® ÀÛ¿ëÀÌ ´Ù¸£´Ù. ¶Ç ¿©·¯ µ¿¹°ÀÇ Å¹ÝÀº ¹ßÁ¤ È£¸£¸ó, Ȳü È£¸£¸óÀ» ºÐºñÇÏ¿© ³­¼ÒÀÇ ³»ºÐºñ Ȱµ¿¿¡ ¿µÇâÀ» ¹ÌÄ¡°í, ³ª¾Æ°¡¼­´Â »ý½Ä°è ÀüüÀÇ Àӽű⿡ ƯÀ¯ÇÑ »óÅÂÀÇ À¯Áö¿¡ °ü¿©Çϰí ÀÖ´Ù. ÄÚ¸£Æ¼ÄÚÀ̵åÀÇ »ý»ê, ºÐºñ °¡´É¼ºµµ Á¡Â÷ ÀÎÁ¤µÇ¾î ÀÌµé ¿©·¯ °¡Áö È£¸£¸ó ºÐºñ Á¶Á÷¿¡ °üÇÑ ¿¬±¸µµ ÁøÇàµÇ°í ÀÖ´Ù.
  • pressure receptor
    ¾Ð¼ö¿ë±â, ¾Ð·Â¼ö¿ëü
    µ¿ÀǾî=
  • receptor
    ¼ö¿ë±â, ¼ö¿ëü, °¨¼öü
    1. ¼¼Æ÷Áú ³» ¶Ç´Â ¼¼Æ÷ Ç¥¸é¿¡ Á¸ÀçÇÏ´Â ºÐÀÚ ±¸Á¶·Î¼­
  • receptor activation
    ¼ö¿ëü Ȱ¼ºÈ­, ¼ö¿ë±â Ȱ¼ºÈ­
  • receptor blocking agent
    ¼ö¿ëü Â÷´ÜÁ¦
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
glycine receptor <physiology> Chloride channel forming receptor. One of a family of neurotransmitter receptors with fast intrinsic ion channels.
See: amino acid receptors.
(18 Nov 1997)
peptide receptor Specific receptor for peptide neurotransmitters.
(18 Nov 1997)
G-protein coupled receptor <cell biology> Cell surface receptors that are coupled to G-proteins (GTP-binding protein).
G-protein coupled receptors are thought to have seven membrane spanning domains and have been divided into 2 subclasses: those in which the binding site is in the extracellular domain for example receptors for glycoprotein hormones, such as thyroid stimulating hormone (TSH) and follicle-stimulating hormone (FSH) and those in which the ligand binding site is likely to be in the plane of the 7 transmembrane domains for example rhodopsin and receptors for small neurotransmitters and hormones for example muscarinic acetylcholine receptor.
(18 Nov 1997)
chemokine receptor A molecule that receives a chemokine and a chemokine dock. Several chemokine receptors are essential co-receptors for HIV.
(12 Dec 1998)
metabotropic receptor A type of receptor that is linked to intracellular production of 1,2-diacylglycerol and inositol 1,4,5-trisphosphate.
Origin: metabolism + G. Trope, turning, inclination, + -ic
(05 Mar 2000)
ryanodine receptor calcium release channel Protein complexes that mediate the release of calcium from the sarcoplasmic reticulum in both skeletal and cardiac muscle cells by forming tetrametric complexes. These complexes each then act as a calcium channel. There are three isoforms of the ryr: ryr1, ryr2, and ryr3. Ryr1 is specifically expressed in skeletal muscles and ryr2 in cardiac muscles. Ryr3 is yet another isoform found in non-muscle cells such as neuronal cells.
(12 Dec 1998)
PL7a receptor-tyrosine kinase <enzyme> A member of the eph receptor tyrosine kinase subfamily; shows 80% identity with myk-1; genbank l43622
Registry number: EC 2.7.1.-
Synonym: pl7a protein
(26 Jun 1999)
Con A receptor <biochemistry> A common misuse of the term receptor. Con A binds to the mannose residues of many different glycoproteins and glycolipids and the binding is therefore not to a specific site.
It could be argued that the receptor is the Con A and cells have Con A ligands on their surfaces: certainly this would be less confusing.
(05 Jan 1998)
muscarinic acetylcholine receptor Distinct from the nicotinic ACh receptor in having no intrinsic ion channel, the receptor is formed from one protein chain with 7 transmembrane regions. The receptors produce their effect via activation of GTP-binding proteins.
(18 Nov 1997)
muscarinic receptor kinase <enzyme> Phosphorylates muscarinic acetylcholine receptors and beta-adrenergic receptors
Registry number: EC 2.7.-
Synonym: muscarinic acetylcholine receptor kinase, machr kinase
(26 Jun 1999)
cyclic AMP receptor protein A transcriptional regulator in prokaryotes which, when activated by binding cyclic AMP, acts at several promoters. Cyclic AMP receptor protein was originally identified as a catabolite gene activator protein. It was subsequently shown to regulate several functions unrelated to catabolism, and to be both a negative and a positive regulator of transcription. Cell surface cyclic AMP receptors are not included (cyclic AMP receptors), nor are the eukaryotic cytoplasmic cyclic AMP receptor proteins, which are the regulatory subunits of cyclic AMP-dependent protein kinases.
(12 Dec 1998)
presynaptic receptor <physiology> Receptors located on presynaptic terminals at synapses.
(05 Mar 1998)
progesterone receptor assay The progesterone receptor test (PgR assay) checks the tumour for its hormone status.
(16 Dec 1997)
Xiphophorus melanoma receptor kinase <enzyme> Growth factor receptor protein with an extracellular ligand binding domain and an intracellular catalytic domain
Registry number: EC 2.7.1.-
Synonym: xmrk protein
(26 Jun 1999)
selective oestrogen-receptor modulator <pharmacology> An antioestrogen which possesses some, but not all, of the actions of oestrogen. For example, raloxifene (evista) is classified as a SERM because it prevents bone loss (like oestrogen) and lowers serum cholesterol (like oestrogen) but (unlike oestrogen) does not stimulate the endometrial lining of the uterus.
Acronym: SERM
(17 Jul 2002)
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