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"Genes, Wilms Tumor"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 5
  • ¿µ¹®
    ÇѱÛ
  • virilizing tumor
    ³²¼ºÈ­Á¾¾ç
  • virus-induced tumor
    ¹ÙÀÌ·¯½ºÀ¯¹ßÁ¾¾ç
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 3 ÆäÀÌÁö: 5
  • ¿µ¹®
    ÇѱÛ
  • renal pelvic tumor
    ½Å¿ìÁ¾¾ç
  • renal pelvic tumor
    ½Å¿ìÁ¾¾ç(ãìéâðþåË)
  • renin-secreting juxtaglomerular tumor
    ·¹´ÑºÐºñ¼º¹æ»ç±¸Ã¼Á¾¾ç
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
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    ÇѱÛ
  • carotid body tumor
    °æµ¿¸Æ¼ÒüÁ¾¾ç(ÌòÔÑØæá³ô÷ðþåË), °æµ¿¸Æ±¸Á¾¾ç(¡­Ï¹ðþåË)
  • cartilaginous tumor
    ¿¬°ñ¼º Á¾¾ç(æãÍéàõðþåË).
  • cavernous tumor =cavernoma
    ÇØ¸é»óÁ¾¾ç, ÇØ¸éÁ¾.
  • cerebellopontine angle tumor
    ¼Ò³ú±³°¢(ºÎ)Á¾¾ç
  • cerebellopontine tumor
    ¼Ò³ú±³°¢Á¾¾ç(¡­ðþåË).
  • congenital intracranial tumor
    ¼±Ãµ¼º µÎ°³(°­)³»Á¾¾ç(¡­ÔéËÏË·Ò®ðþ åË).
  • cutaneous cartilaginous tumor
    ÇǺΠ¿¬°ñ¼º((ù«Ý±)æãÍéàõ) Á¾¾ç(ðþåË)
  • cutaneous tumor
    ÇǺÎÁ¾¾ç
  • deep seated tumor
    ½ÉÀ缺Á¾¾ç
  • deficiency (monstrous tumor)
    °áÇÌ (±«¹°Á¾)
  • delta cell tumor
    µ¨Å¸ ¼¼Æ÷ Á¾¾ç(¡­á¬øàðþåË)
  • demblee tumor
    Àü°ÝÇü Á¾¾ç
  • dermal duct tumor
    ÁøÇǵµ°üÁ¾¾ç
  • dermal tumor
    ÁøÇÇÁ¾¾ç
  • desmoid tumor
    µ¥½º¸ðÀ̵åÁ¾¾ç, Àδë¸ð¾çÁ¾¾ç(ìåÓáåÆðþåË).
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TSA technical surgical assistance; toluene sulfonic acid; total shoulder arthroplasty; total solute abso...
TSTA toxoplasmin skin test antigen; tumor-specific tissue antigen; tumor-specific transplantation antigen...
CEA Carcino-Embryonic Antigen [HP 1825-6]
  ; Oncofetal Antigens
  ; Glycopro...
GTT   1) Gestational Trophoblastic Tumor
  2) Glucose Tolerance Test; ´çºÎÇϰ˻ç
HIVD Herniation(Herniated) of Inter-Vertebral Disc
  - Cervical HIVD
   &...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 5
EST Endodermal sinus tumor
enTNF Endogenous tumor necrosis factor
ET Ewing tumor
GANT Gastrointestinal autonomic nerve tumor
GITSG Gastrointestinal Tumor Study Group
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
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    ¼³¸í
  • mucous tumor
    Á¡¾×Á¾
  • multiple vascular tumor
    ´Ù¹ß¼º Ç÷°ü Á¾¾ç
  • nasopharyngeal tumor
    ºñ ÀεΠÁ¾¾ç
  • nerve tumor
    ½Å°æ Á¾¾ç
  • neuroectodermal tumor
    ½Å°æ ¿Ü¹è¿± Á¾¾ç
  • neuroendocrine tumor
    ½Å°æ ³»ºÐºñÁ¾
  • neuroglial tumor
    ½Å°æ±³ Á¾¾ç
  • nevoid tumor
    ¸ð¹Ý¾ç Á¾¾ç
  • nonclassifed tumor
    ºÐ·ùµÇÁö ¾Ê´Â Á¾¾ç
  • nonodontogenic malignant tumor jaw
    ºñÄ¡¾Æ¼º ¾Ç¼º Á¾¾ç
  • odontogenic mixed tumor
    Ä¡¿ø È¥ÇÕ Á¾¾ç
  • ovarian tumor
    ³­¼Ò Á¾¾ç
    ³­¼Ò¿¡¼­ »ý±â´Â Á¾¾ç. ³­¼Ò´Â ÀÎüÀÇ Àå±â Áß¿¡¼­ °¡Àå ¸¹Àº Á¾·ùÀÇ Á¾¾çÀÌ ¹ß»ýÇÏ´Â ±â°üÀÌ¸ç ±× ºÐ·ù¹ýµµ ´Ù¾çÇØ, ¿©·¯ °¡Áö À̸§À¸·Î ºÒ¸°´Ù. ÀÓ»óÀûÀ¸·Î´Â ¾ç¼º, ¾Ç¼º, Áß°£¼ºÀÇ ¼¼ °¡Áö·Î ´ëº°µÇÁö¸¸ °¨º°ÀÌ °ï¶õÇÑ °æ¿ìµµ ÀÖ´Ù. ´ëü·Î Ãæ½ÇºÎ°¡ ÀüÇô ¾ø´Â ¼ø³¶Æ÷¼ºÀÇ °ÍÀ» ³¶Æ÷¼º Á¾¾çÀ̶ó ÇÏ¸ç ¾ç¼ºÀÌ´Ù. Ãæ½ÇºÎ·Î µÇ¾î ÀÖ´Â °æ¿ì¸¦ Ãæ½Ç¼º Á¾¾çÀ̶ó Çϸç, ³¶Æ÷ºÎ¿Í Ãæ½ÇºÎ°¡ ¼¯¿© ÀÖ´Â °æ¿ì¸¦ ¹ÝÃæ½Ç¼º Á¾¾çÀ̶ó Çϴµ¥ ÀÌ µÎ °¡Áö¸¦ ÇÕÃļ­ Ãæ½Ç¼º Á¾¾çÀ̶ó ÇÑ´Ù.
  • papillomatous tumor
    À¯µÎ¼º Á¾¾ç
  • paratesticular tumor
    °íȯ¹æ Á¾¾ç
  • pea-size tumor
    °­³²Äá Å©±âÀÇ Á¾¾ç
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 5
genes, reporter Genes whose expression is easily detectable and therefore used to study promoter activity at many positions in a target genome. In recombinant DNA technology, these genes may be attached to a promoter region of interest.
(12 Dec 1998)
genes, retinoblastoma Tumour suppressor genes located on human chromosome 13 in the region 13q14 and coding for a family of phosphoproteins with molecular weights ranging from 104 kD to 115 kD. One copy of the wild-type rb gene is necessary for normal retinal development. Loss or inactivation of both alleles at this locus results in retinoblastoma.
(12 Dec 1998)
genes, rev DNA sequences that form the coding region for a protein that regulates the expression of the viral structural and regulatory proteins in human immunodeficiency virus (HIV). Rev is short for regulator of virion.
(12 Dec 1998)
genes, src Retrovirus-associated DNA sequences (src) originally isolated from the rous sarcoma virus (rsv). The proto-oncogene src (c-src) codes for a protein that is a member of the tyrosine kinase family and was the first proto-oncogene identified in the human genome. The human c-src gene is located at 20q12-13 on the long arm of chromosome 20.
(12 Dec 1998)
genes, structural Genes that code for proteins required for the enzymatic and structural functions of cells. They include developmental and differentiated genes.
(12 Dec 1998)
genes, structural, bacterial DNA sequences that code for RNA and for the proteins required for the enzymatic and structural function of bacterial cells.
(12 Dec 1998)
genes, structural, fungal DNA sequences that code for RNA and for the proteins required for the enzymatic and structural function of fungal cells.
(12 Dec 1998)
genes, structural, helminth DNA sequences that code for RNA and for the proteins required for the enzymatic and structural function of helminthic cells.
(12 Dec 1998)
genes, structural, insect DNA sequences that code for RNA and for proteins required for the enzymatic and structural function of insect cells.
(12 Dec 1998)
genes, structural, neoplasm DNA sequences that code for RNA and for the proteins required for the enzymatic and structural function of neoplastic cells.
(12 Dec 1998)
genes, structural, plant DNA sequences that code for RNA and for the proteins required for the enzymatic and structural function of plant cells.
(12 Dec 1998)
genes, structural, protozoan DNA sequences that code for RNA and for the proteins required for the enzymatic and structural function of protozoan cells.
(12 Dec 1998)
genes, structural, viral DNA or RNA sequences that code for RNA and for the proteins required for the enzymatic and structural function of viral cells.
(12 Dec 1998)
genes, suppressor Genes that inhibit expression of a previous mutation. They allow the wild-type phenotype to be wholly or partially restored.
(12 Dec 1998)
genes, suppressor, tumour Genes that inhibit expression of the tumourigenic phenotype. They are normally involved in holding cellular growth in check. When tumour suppressor genes are inactivated or lost, a barrier to normal proliferation is removed and deregulated growth is possible.
(12 Dec 1998)
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