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PUBMED FOR HANDHELDS

Journal Abstract Search


111 related items for PubMed ID: 1372103

  • 21. Effect of XPA gene mutations on UV-induced immunostaining of PCNA in fibroblasts from xeroderma pigmentosum group A patients.
    Miura M, Sasaki T.
    Mutat Res; 1996 Sep 02; 364(1):51-6. PubMed ID: 8814338
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  • 22. Cloning and characterization of the mouse XPAC gene.
    van Oostrom CT, de Vries A, Verbeek SJ, van Kreijl CF, van Steeg H.
    Nucleic Acids Res; 1994 Jan 11; 22(1):11-4. PubMed ID: 8127648
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  • 23. A mutation in repB, the dictyostelium homolog of the human xeroderma pigmentosum B gene, has increased sensitivity to UV-light but normal morphogenesis.
    Lee SK, Yu SL, Alexander H, Alexander S.
    Biochim Biophys Acta; 1998 Aug 20; 1399(2-3):161-72. PubMed ID: 9765592
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  • 24. Two novel splicing mutations in the XPA gene in patients with group A xeroderma pigmentosum.
    Satokata I, Uchiyama M, Tanaka K.
    Hum Mol Genet; 1995 Oct 20; 4(10):1993-4. PubMed ID: 8595429
    [No Abstract] [Full Text] [Related]

  • 25. Characterization of molecular defects in xeroderma pigmentosum group C.
    Li L, Bales ES, Peterson CA, Legerski RJ.
    Nat Genet; 1993 Dec 20; 5(4):413-7. PubMed ID: 8298653
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  • 33. DNA-based prenatal diagnosis in a Chinese family with xeroderma pigmentosum group A.
    Yang Y, Ding B, Wang K, Bu D, Tu P, Zhu X.
    Br J Dermatol; 2004 Jun 20; 150(6):1190-3. PubMed ID: 15214909
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  • 35. A novel XPA gene mutation and its functional analysis in a Japanese patient with xeroderma pigmentosum group A.
    Tanioka M, Budiyant A, Ueda T, Nagano T, Ichihashi M, Miyachi Y, Nishigori C.
    J Invest Dermatol; 2005 Aug 20; 125(2):244-6. PubMed ID: 16098033
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  • 36. Identification of four novel XPC mutations in two xeroderma pigmentosum complementation group C patients and functional study of XPC Q320X mutant.
    Gu Y, Chang X, Dai S, Song Q, Zhao H, Lei P.
    Gene; 2017 Sep 10; 628():162-169. PubMed ID: 28669926
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  • 38. Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient.
    Nouspikel T, Clarkson SG.
    Hum Mol Genet; 1994 Jun 10; 3(6):963-7. PubMed ID: 7951246
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