xeroderma pigmentosum

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英 [ˌpɪgmənˈtəʊsəm]
美 [ˌpɪɡmənˈtosəm]
是什么意思
  • 释义

    着色性干皮病;

  • 英英释义

    xeroderma pigmentosum

    • n.a rare genetic condition characterized by an eruption of exposed skin occurring in childhood and photosensitivity with severe sunburn; inherited as a recessive autosomal trait in which DNA repair processes are defective so they are more likely to chromosome breaks and cancers when exposed to ultraviolet light
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    权威例句

    Xeroderma pigmentosum
    Xeroderma pigmentosum
    Xeroderma Pigmentosum.
    Xeroderma pigmentosum (XP)
    The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta
    hRAD30 mutations in the variant form of xeroderma pigmentosum.
    Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair
    Xeroderma pigmentosum variant (XP-V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity.
    Cleaver JE. Defective repair replications of DNA in xeroderma pigmentosum
    Activated Oncogenes in Human Skin Tumors from a Repair-deficient Syndrome, Xeroderma Pigmentosum
    The role of sunlight and DNA repair in melanoma and nonmelanoma skin cancer. The xeroderma pigmentosum paradigm.
    Establishment and characterization of a melanoma cell line from a xeroderma pigmentosum patient: activation of N-ras at a potential ...
    Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human hom...
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