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  • ¿µ¹®
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  • caretaker genes
    °ü¸®À¯ÀüÀÚ
  • homologous genes
    »óµ¿À¯ÀüÀÚ
  • exophytic retinoblastoma
    ¿Ü¼ºÀå¸Á¸·¸ð¼¼Æ÷Á¾
  • endophytic retinoblastoma
    ³»¼ºÀå¸Á¸·¸ð¼¼Æ÷Á¾
  • retinoblastoma
    ¸Á¸·¸ð¼¼Æ÷Á¾
  • retinoblastoma gene
    ¸Á¸·¸ð¼¼Æ÷Á¾À¯ÀüÀÚ
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  • ¿µ¹®
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  • endophytic retinoblastoma
    ³»¼ºÀå¸Á¸·¸ð¼¼Æ÷Á¾
  • exophytic retinoblastoma
    ¿Ü¼ºÀå¸Á¸·¸ð¼¼Æ÷Á¾
  • retinoblastoma gene
    ¸Á¸·¸ð¼¼Æ÷Á¾À¯ÀüÀÚ
  • retinoblastoma
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  • hox genes
    Ȥ½º À¯ÀüÀÚ, Hox À¯ÀüÀÚ
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  • retinoblastoma(RB) genes
    ¸Á¸·¾Æ¼¼Æ÷Á¾ À¯ÀüÀÚ
  • endophytic retinoblastoma
    ³»¼ºÀå¸Á¸·¸ð¼¼Æ÷Á¾, ³»Áõ½Ä¸Á¸·¸ð¼¼Æ÷Á¾
  • retinoblastoma
    ¸Á¸·¸ð¼¼Æ÷Á¾(¡­Ù½á¬øàðþ)
  • retinoblastoma endophytum
    ³»¼ºÀå¸Á¸·¸ð¼¼Æ÷Á¾, ³»Áõ½Ä¸Á¸·¸ð¼¼Æ÷Á¾
  • retinoblastoma exophytum
    ¿Ü¼ºÀå¸Á¸·¸ð¼¼Æ÷Á¾, ¿ÜÁõ½Ä¸Á¸·¸ð¼¼Æ÷Á¾
  • c2 genes
    C2 À¯ÀüÀÚ (¡­ë¶îîí­)
  • cancer suppressor genes
    ¾Ï¾ïÁ¦À¯ÀüÀÚ(äßåäð¤ë¶îîí­)
  • ced genes
    ced À¯ÀüÀÚ(¡­ë¶îîí­)
  • complementary genes
    »óº¸¼ºÀ¯ÀüÀÚ(ßÀÜÍàõë¶îîí­).
  • cooperating genes
    Çùµ¿À¯ÀüÀÚ
  • fcc genes
    FCC À¯ÀüÀÚ
  • hox genes
    Ȥ½º À¯ÀüÀÚ, Hox À¯ÀüÀÚ
  • multiple genes
    ´ÙÀ¯ÀüÀÚ.
  • multiple genes
    º¹¼öÀ¯ÀüÀÚ.
  • myogenic genes
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  • C genes
    C À¯ÀüÀÚ(ë¶îîí­)
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    »óº¸¼º À¯ÀüÀÚ(ßÓÜÍàõë¶îîí­)
  • housekeeping genes
    »ì¸² À¯ÀüÀÚ(ë¶îîí­)
  • J genes
    J À¯ÀüÀÚ(ë¶îîí­)
  • joining genes
    Á¢ÇÕÀ¯ÀüÀÚ(ïÈùêë¶îîí­)
  • luxury genes
    ƯȰÀ¯ÀüÀÚ(÷åüÀë¶îîí­)
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    ¹Ýº¹ À¯ÀüÀÚ(ÚãÜÖë¶îîí­)
  • syn genes
    ½Å À¯ÀüÀÚ(ë¶îîí­)
  • syntenic genes
    µ¿¿°»öü À¯ÀüÀÚ(ÔÒæøßäô÷ë¶îîí­)
  • two-genes-one-polypeptide chain
    ÀÌÀ¯ÀüÀÚ(ì£ë¶îîí­)- ÀÏ(ìé)Æú¸®ÆéŸÀÌµå »ç½½
  • ur genes
    ¿ø(ê«) À¯ÀüÀÚ
  • variable genes
    °¡º¯ºÎÀ§(ʦܨݻêÈ) À¯ÀüÀÚ (ë¶îîí­)
  • V genes
    V À¯ÀüÀÚ (ë¶îîí­)
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RB radiation burn; rating board; rebreathing; reticulate body; retinoblastoma; right bronchus; right bu...
Rb retinoblastoma; rubidium
RBBP retinoblastoma binding protein
RBL rat basophilic leukemia; Reid baseline; retinoblastoma-like
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
RCE 3'-retinoblastoma control element
RB Retinoblastoma
RB-1 Retinoblastoma
RB retinoblastoma susceptibility
ISG IFN stimulated genes
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
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)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
retinoblastoma <oncology, tumour> Malignant tumour of the retina, usually arising in the inner nuclear layer of the neural retina.
Retinoblastoma is unusual in being caused by an autosomal dominant mutation in some cases (about 6%), in which case it may be bilateral.
The gene product of the retinoblastoma gene is a tumour suppressor that interacts with transcription factors such as E2F to block transcription of growth regulating genes. The Rb gene plays a role in normal development, not just that of the retina.
Inheritance: autosomal dominant.
(03 Jul 1999)
retinoblastoma protein <molecular biology, protein> Product of the retinoblastoma tumour suppressor gene.
It is a nuclear phosphoprotein hypothesised to normally act as an inhibitor of cell proliferation. Rb protein is absent in retinoblastoma cell lines. It also has been shown to form complexes with the adenovirus e1a protein, the sv40 t antigen, and the human papilloma virus e7 protein.
(03 Jul 1999)
breast cancer susceptibility genes Inherited factors that predispose to breast cancer. Put otherwise, these genes make one more susceptible to the disease and so increase the risk of developing breast cancer. Two of these genes, BRCA1 and BRCA2, have been identified (and prominently publicised). Several other genes (those for the Li-Fraumeni syndrome, Cowden disease, Muir-Torre syndrome, and ataxia-telangiectasia) are also known to predispose to breast cancer. However, since all of these known breast cancer susceptibility genes together do not account for more than a minor fraction (1/5th at most) of breast cancer that clusters in families, it is clear that more breast cancer genes remain to be discovered.
(12 Dec 1998)
cancer, breast, susceptibility genes Inherited factors that predispose to breast cancer. Put otherwise, these genes make one more susceptible to the disease and so increase the risk of developing breast cancer. Two of these genes, BRCA1 and BRCA2, have been identified (and prominently publicised). Several other genes (those for the Li-Fraumeni syndrome, Cowden disease, Muir-Torre syndrome, and ataxia-telangiectasia) are also known to predispose to breast cancer. However, since all of these known breast cancer susceptibility genes together do not account for more than a minor fraction (1/5th at most) of breast cancer that clusters in families, it is clear that more breast cancer genes remain to be discovered.
(12 Dec 1998)
genes Located in the nucleus of the cell, genes contain hereditary information that is transferred from cell to cell.
(09 Oct 1997)
genes, abl Retrovirus-associated DNA sequences (abl) originally isolated from the abelson murine leukaemia virus (ab-mulv). The proto-oncogene abl (c-abl) codes for a protein that is a member of the tyrosine kinase family. The human c-abl gene is located at 9q34.1 on the long arm of chromosome 9. It is activated by translocation to bcr on chromosome 22 in chronic myelogenous leukaemia.
(12 Dec 1998)
genes, apc Tumour suppressor genes located in the 5q21 region on the long arm of chromosome 5. The mutation of these genes is associated with familial adenomatous polyposis (apc stands for adenomatous polyposis coli) and gardner's syndrome, as well as some sporadic colourectal cancers.
(12 Dec 1998)
genes, arac Regulatory genes which encode a cyclic AMP receptor protein required for l-arabinose utilization in e. Coli. It is an example of positive control or regulation of gene expression in the bacterial operon.
(12 Dec 1998)
genes, archaeal The genetic material of archaea.
(12 Dec 1998)
genes, bacterial The genetic material of bacteria.
(12 Dec 1998)
genes, bcl-1 The B-cell leukaemia/lymphoma-1 genes, associated with various neoplasms when overexpressed. Overexpression results from the t(11;14) translocation, which is characteristic of mantle zone-derived B-cell lymphomas. The human c-bcl-1 gene is located at 11q13 on the long arm of chromosome 18.
(12 Dec 1998)
genes, bcl-2 The B-cell leukaemia/lymphoma-2 genes, responsible for blocking apoptosis in normal cells, and associated with follicular lymphoma when overexpressed. Overexpression results from the t(14;18) translocation. The human c-bcl-2 gene is located at 18q24 on the long arm of chromosome 18.
(12 Dec 1998)
genes, BRCA1 Tumour suppressor genes located on human chromosome 17q12-21. The mutation of these genes is associated with the formation of familial breast and ovarian cancer.
(12 Dec 1998)
genes, breast cancer susceptibility Inherited factors that predispose to breast cancer. Put otherwise, these genes make one more susceptible to the disease and so increase the risk of developing breast cancer. Two of these genes, BRCA1 and BRCA2, have been identified (and prominently publicised). Several other genes (those for the Li-Fraumeni syndrome, Cowden disease, Muir-Torre syndrome, and ataxia-telangiectasia) are also known to predispose to breast cancer. Howeverm, since all of these known breast cancer susceptibility genes together do not account for more than a minor fraction (1/5th at most) of breast cancer that clusters in families, it is clear that more breast cancer genes remain to be discovered. See related entries to: BRCA1; BRCA2; Breast cancer, familial.
(12 Dec 1998)
genes, cdc Genes that code for proteins that regulate the cell division cycle. These genes form a regulatory network that culminates in the onset of mitosis by activating the p34cdc2 protein (protein p34cdc2).
(12 Dec 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Genes, Retinoblastoma - »õâ Tumor suppressor genes located on human chromosome 13 in the region 13q14 and coding for a family of phosphoproteins with molecular weights ranging from 104 kDa to 115 kDa. 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.
    Synonyms : Gene, Rb, Gene, Retinoblastoma, Rb Gene, Retinoblastoma Gene
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