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    ÇѱÛ
  • genetic mutation
    À¯Àüµ¹¿¬º¯ÀÌ
  • genetic psychology
    À¯Àü½É¸®ÇÐ
  • genetic reactivation
    À¯ÀüÀûÀçȰ¼ºÈ­
  • genetic reassortment
    À¯ÀüÀÚÀçÆí¼º, À¯ÀüÀÚÀçÁýÇÕ
  • genetic recombination
    À¯ÀüÀÚÀçÁ¶ÇÕ
  • genetic regulation
    À¯ÀüÀûÁ¶Àý
  • genetic resistance
    À¯ÀüÀúÇ×
  • genetic restriction
    À¯Àü»óÈ£ÀÛ¿ëÁ¦ÇÑ
  • genetic screening
    À¯Àü¼±º°°Ë»ç
  • genetic sex
    1. À¯ÀüÀû¼º 2. À¯ÀüÀû¼ºº°
  • genetic susceptibility
    À¯ÀüÀû°¨¼ö¼º
  • molecular genetic study
    ºÐÀÚÀ¯ÀüÇа˻ç
  • multifactorial genetic disorder
    ´ÙÀÎÀÚÀ¯ÀüÁúȯ
  • associated defect
    ¿¬°üÀå¾Ö
  • atrial septal defect
    ½É¹æ»çÀ̸·°á¼Õ, ½É¹æÁ߰ݰá¼Õ
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  • ¿µ¹®
    ÇѱÛ
  • genetic information
    À¯ÀüÁ¤º¸
  • genetic instability
    À¯ÀüºÒ¾ÈÁ¤
  • genetic interaction
    À¯Àü»óÈ£ÀÛ¿ë
  • genetic linkage
    À¯ÀüÀû°ü·Ã¼º
  • genetic load
    À¯ÀüÇÏÁß
  • genetic mutation
    À¯Àüµ¹¿¬º¯ÀÌ
  • genetic psychology
    À¯Àü½É¸®ÇÐ
  • genetic reactivation
    À¯ÀüÀçȰ¼ºÈ­
  • genetic reassortment
    À¯ÀüÀÚÀçÆí¼º, À¯ÀüÀÚÀçÁýÇÕ
  • genetic recombination
    (¢¡gene recombination) À¯ÀüÀÚÀçÁ¶ÇÕ
  • genetic regulation
    À¯ÀüÀûÁ¶Àý
  • genetic resistance
    À¯ÀüÀúÇ×
  • genetic restriction
    À¯ÀüÀû»óÈ£ÀÛ¿ëÁ¦ÇÑ
  • genetic sex
    À¯ÀüÀû¼º
  • genetic susceptibility
    À¯ÀüÀÚ°¨¼ö¼º, À¯ÀüÀû°¨¼ö¼º
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  • ¿µ¹®
    ÇѱÛ
  • heritable defect
    À¯Àü°áÇÔ
  • high ventricular septal defect
    °íÀ§½É½ÇÁ߰ݰá¼Õ.
  • placental defect
    ŹݰáÇÔ
  • plication defect
    ÁÖ¸§Çü¼º°áÇÔ
  • plication defect (schistomyelia)
    ÁÖ¸§Çü¼º°áÇÔ (ô¼ö°¥¸²Áõ)
  • postnatal defect
    Ãâ»ýÀÌÈİáÇÔ
  • prenatal defect
    Ãâ»ýÀÌÀü°áÇÔ
  • primum atrial septal defect
    ÀÏÂ÷°ø½É¹æÁ߰ݰá¼Õ(Áõ).
  • primum atrial septal defect
    ÀÏÂ÷°ø½É¹æÁ߰ݰá¼Õ(Áõ)(ìéó­°ø½É¹æÁß°ÝÌÀáß(ñø))
  • promeiotic defect
    °¨¼öºÐ¿­ÀÌÀü°áÇÔ
  • quantum defect
    ¾çÀÚ°á¼Õ.
  • relative afferent pupillary defect
    »ó´ëÀû±¸½É¼ºµ¿°ø¿îµ¿Àå¾Ö
  • remediable defect
    Ä¡À¯°¡´É°áÇÔ(ö½ë¨Ê¦ÒöÌÀùè).
  • remediable defect
    Ä¡À¯°¡´É°áÇÔ(ö½ë¨Ê¦ÒöÌÀùè)
  • Genetic abnomnalities, disoders caused by
    À¯ÀüÀÚÀÌ»ó(¡­ì¶ßÈ)
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  • ¿µ¹®
    ÇѱÛ
  • symport= co- transport
    °øµ¿¿î¹Ý(ÍìÔÒê¡Úæ)
  • transcapillary transport
    ¸ð¼¼°ü¿î¹Ý (¡­ê¡Úæ)
  • transcapillary transport
    ¸ð¼¼°ü¿î¹Ý (¡­ê¡Úæ).
  • transmembrane transport
    ¸· Åë°ú À̵¿
  • transport maxima
    ÃÖ´ëÀ̵¿Ä¡(õÌÓÞì¹ÔÑö·).
  • transport maximum
    ÃÖ´ëÀ̵¿Ä¡(õÌÓÞì¹ÔÑö·)
  • transport maximum of glucose
    Æ÷µµ´ç(øãÔ¬ÓØ)À̵¿ÃÖ°íÄ¡.
  • transport medium
    ¼ö¼Û¹èÁö(âÃáêÛÆò¢).
  • transport number
    À̵¿·ü.
  • transport of materials
    ¹°ÁúÀ̵¿(Úªòõì¹ÔÑ).
  • transport oxygen
    »ê¼Ò¿î¹Ý(ß«áÈê¡Úæ).
  • transport phenomenon
    ¹°ÁúÀ̵¿Çö»ó (¡­úÞßÚ).
  • transport system
    Àü´Þ°è
  • tubular transport maximum
    ¼¼´¢°üÀ̵¿ÃÖ°íÄ¡(¡­ì¹ÔÑõÌÍÔö·)
  • tubular transport maximum
    ¼¼´¢°üÀ̵¿ÃÖ°íÄ¡(¡­ì¹ÔÑõÌÍÔö·).
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  • ¿µ¹®
    ÇѱÛ
  • Defect of fertilization
    ¼öÁ¤°áÇÔ
    [¿¾ ¿ë¾î] ¼öÁ¤°áÇÔ
  • Metabolic defect of steroid (Adrenogenital syndrome)
    ½ºÅ×·ÎÀ̵å´ë»ç°áÇÔ(ºÎ½Å»ý½Ä±âÁõÈıº)
    [¿¾ ¿ë¾î] ½ºÅ×·ÎÀ̵å´ë»ç°áÇÔ(ºÎ½Å»ý½Ä±âÁõÈıº)
  • Neural defect (Imbecility)
    ½Å°æ°áÇÌ(Ä¡¿ì)
    [¿¾ ¿ë¾î] ½Å°æ°áÇÔ
  • Ventricular septal defect
    ½É½Ç»çÀ̸·°áÇÔ
    [¿¾ ¿ë¾î] ½É½ÇÁ߰ݰáÇÔ
  • Defect of heart
    ½ÉÀå°áÇÔ
    [¿¾ ¿ë¾î] ½ÉÀå°áÇÔ
  • Heart defect
    ½ÉÀå°áÇÔ
    [¿¾ ¿ë¾î] ½ÉÀå°áÇÔ
  • Metabolic defect of amino acid (Alkaptonuria)
    ¾Æ¹Ì³ë»ê´ë»ç°áÇÔ(¾Ëİſ´¢Áõ)
    [¿¾ ¿ë¾î] ¾Æ¹Ì³ë»ê´ë»ç°áÇÔ(¾Ëİſ´¢Áõ)
  • Amniotic defect
    ¾ç¸·°áÇÔ
    [¿¾ ¿ë¾î] ¾ç¸·°áÇÔ
  • Facial defect
    ¾ó±¼°áÇÔ
    [¿¾ ¿ë¾î] ¾È¸é°áÇÔ
  • Chromosomal defect
    ¿°»öü°áÇÔ
    [¿¾ ¿ë¾î] ¿°»öü°áÇÔ
  • Heritable defect
    À¯Àü°áÇÔ
    [¿¾ ¿ë¾î] À¯Àü¼º°áÇÔ
  • Fusion defect
    À¶ÇÕ°áÇÔ
    [¿¾ ¿ë¾î] À¶ÇÕ°áÇÔ
  • Fusion defect (Cleft palate)
    À¶ÇÕ°áÇÔ (ÀÔõÀå°¥¸²Áõ)
    [¿¾ ¿ë¾î] À¶ÇÕ°áÇÔ (ÀÔõÀå°¥¸²Áõ)
  • Aggregation defect
    ÀÀÁý°áÇÔ
    [¿¾ ¿ë¾î] ÀÀÁý¼º°áÇÔ
  • Migration defect
    ÀÌÁÖ°áÇÔ
    [¿¾ ¿ë¾î] ÀÌÁÖ°áÇÔ
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  • ¿µ¹®
    ÇѱÛ
  • anion-transport protein
    À½À̿¿î¹Ý(ê¡Úõ) ´Ü¹éÁú(Ó±ÛÜòõ)
  • binding protein transport system
    °áÇÕ ´Ü¹éÁú ¼ö¼Û(Ì¿ùêÓ±ÛÜòõâÃáê) ½Ã½ºÅÛ
  • carbon dioxide transport
    ÀÌ»êȭź¼Ò ¼ö¼Û(ì£ß«ûù÷©áÈâÃáê)
  • cotranslational transport
    ¹ø¿ªµ¿½Ã¼ö¼Û(Ûèæ»ÔÒãÁâÃáê)
  • coupled transport
    "°ø¿ª¼ö¼Û(ÍëæµâÃáê), ¦Áø¼ö¼Û"
  • electron transport chain
    ÀüÀÚ¼ö¼Û(ï³í­âÃáê) »ç½½
  • electron transport particle
    ÀüÀÚ¼ö¼Û ÀÔÀÚ(ï³í­âÃáêØ£í­)
  • electron transport system
    ÀüÀÚ¼ö¼Û(ï³í­âÃáê) ½Ã½ºÅÛ
  • fractional electrical transport
    ºÐº° Àü±â ¼ö¼Û(ÝÂܬï³Ñ¨âÃáê)
  • gradient-coupled active transport
    ±¸¹è(ÎþÛÕ) ¦Áø ´Éµ¿¼ö¼Û(ÒöÔÑâÃáê)
  • homocellular transport
    µ¿Áú¼¼Æ÷ ¼ö¼Û(ÔÒòõá¬øàâÃáê)
  • hydrogen transport system
    ¼ö¼Ò ¼ö¼Û(â©áÈâÃáê) ½Ã½ºÅÛ
  • illicit transport
    ¹Ð¼ö¼Û(ÚËâÃáê)
  • intracellular transport
    ¼¼Æ÷³» ¼ö¼Û(á¬øàÒ®âÃáê)
  • mediated transport
    ¸Å°³¼ö¼Û(ØÚË¿âÃáê)
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
GM gastric mucosa; Geiger-Muller [counter]; general medicine; genetic manipulation; geometric mean; gia...
GP gangliocytic paraganglioma; gastroplasty; general paralysis, general paresis; general practice, gene...
HGMCR human genetic mutant cell repository
IGA infantile genetic agranulocytosis
VG genetic variance
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 3
MD Mean Defect
PD Perfusion defect
RAPD Relative afferent pupillary defect
TDS Total defect score
VSD Ventricular Septal Defect
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
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    ÇѱÛ
    ¼³¸í
  • interventricular septal defect
    ½É½Ç Áß°Ý °á¼ÕÁõ
  • metabolic defect of amino acid
    ¾Æ¹Ì³ë»ê ´ë»ç °áÇÔ
    ¾Ëİſ ´¢Áõ.
  • metabolic defect of pigment
    »ö¼Ò ´ë»ç °áÇÔ
  • morphologic defect
    ÇüÅ °áÇÔ
  • ostium primum atrial septal defect
    ÀÏÂ÷ °øÇü ½É¹æ Áß°Ý °á¼Õ
  • paraplacental chorionic defect
    ÅÂ¹Ý °ç À¶¸ð¸· °áÇÔ
  • perceptual defect
    Áö°¢ °á¼Õ
  • peroxidase defect
    °ú»êÈ­È¿¼Ò °á¼Õ
  • punch out defect
    ±¸¸Û °á¼Õ
  • qualitative platelet defect
    Á¤»ó Ç÷¼ÒÆÇ °áÇÌÁõ, ÁúÀû Ç÷¼ÒÆÇ °áÇÔ
  • quantum defect
    ¾çÀÚ °á¼Õ
  • skeletal defect
    °ñ°Ý °á¼Õ
  • small atrial septal defect
    ¹Ì¼¼ ½É¹æ Áß°Ý °á¼Õ
  • substance defect
    ¹°Áú °áÇÌ
  • superficial defect
    Ç¥À缺 °á¼Õ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
endocardial cushion defect <radiology> Persistence of primitive atrioventricular canal and anomalies of AV valves associated with: Down syndrome: in 25% of Trisomy 21 an ECD is present; in 45% of ECD Trisomy 21 is present, asplenia/polysplenia types: complete (AV canal), partial findings: gooseneck deformity on angiogram, increased pulmonary vascularity, enlarged pulmonary artery, enlarged RV, LV, RA; normal LA (secondary to atrial septal defect)
(12 Dec 1998)
enzyme defect A disorder resulting from a deficiency (or functional abnormality) of an enzyme. In 1902 Archibald Garrod first attributed a disease to an enzyme defect: an inborn error of metabolism. Today, newborns are routinely screened for certain enzyme defects such as PKU (phenylketonuria) and galactosaemia, an error in the handling (metabolism) of the sugar galactose.
(12 Dec 1998)
fibrous cortical defect A common 1 to 3 cm defect in the cortex of a bone, most commonly the lower femoral shaft of a child, filled with fibrous tissue. Nonosteogenic or nonossifying fibroma by convention refers to lesions greater than 3 cm in diameter.
See: nonossifying fibroma.
Synonym: nonosteogenic fibroma.
(05 Mar 2000)
uterine filling defect <radiology> Technical, bubble, blood clot, mucoid material, congenital fold, pseudoadhesions / ridging -- folds long axis, neoplasm, submucosal leiomyoma, adenoma, endometrial carcinoma, pregnancy-related, pregnancy, molar pregnancy, retained conceptus, polyp, septated uterus, synechiae, IUD, iatrogenic (post-op)
(12 Dec 1998)
filling defect Displacement of contrast medium by a space-occupying lesion in a radiographic study of a contrast-filled hollow viscus, such as a polyp on a barium enema; also applied to defects in the otherwise uniform distribution of radionuclide in an organ, such as a metastasis in the liver on a 99mTc-sulfur colloid scan.
(05 Mar 2000)
filling defect in renal collecting system <radiology> Common causes: transitional cell carcinoma, blood clot, lucent calculus (urate) less common causes: fungus ball, sloughed papilla, fibroepithelial polyp, invasion by hypernephroma, malakoplakia, vessel impression, metastases
(12 Dec 1998)
lambdoid suture defect <radiology> Well-defined lucent lesion, classically unilateral, associated with neurofibromatosis
(12 Dec 1998)
luteal phase defect Inadequate function of the corpus luteum that may prevent a fertilized egg from implanting in the uterus or may lead to early pregnancy loss.
(09 Oct 1997)
active transport <biochemistry, chemistry> Transport of ions, nutrients or other molecules into a cell against a concentration gradient, this requires the expenditure of energy through ATP hydrolysis.
(06 May 1997)
anterograde transport Movement of material from the cell body of a neuron into axons and dendrites retrograde axoplasmic transport also occurs).
(18 Nov 1997)
atrial transport function The role of the atria in filling and stretching the ventricles by their presystolic contraction, without which the force of ventricular contraction and hence the cardiac output may significantly decrease.
(05 Mar 2000)
axonal transport Directed transport of organelles and molecules along a nerve cell axon. Transport can be anterograde (from the cell body) or retrograde (toward the cell body). (alberts et al., molecular biology of the cell, 3d ed, pg3)
(12 Dec 1998)
axoplasmic transport Transport by way of flow of axoplasm toward cell soma (retrograde) or toward axon terminal (anterograde).
(05 Mar 2000)
biological transport The movement of materials (including biochemical substances and drugs) across cell membranes and epithelial layers, usually by passive diffusion.
(12 Dec 1998)
biological transport, active The movement of materials across cell membranes and epithelial layers against an electrochemical gradient, requiring the expenditure of metabolic energy.
(12 Dec 1998)
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