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Journal Abstract Search

103 related items for PubMed ID: 8105118

  • 1. [Neurological manifestations and molecular basis of group A xeroderma pigmentosum].
    Mimaki T, Tanaka K, Nagai A, Mino M.
    Nihon Rinsho; 1993 Sep; 51(9):2488-93. PubMed ID: 8105118
    [Abstract] [Full Text] [Related]

  • 2. Gene alterations and clinical characteristics of xeroderma pigmentosum group A patients in Japan.
    Nishigori C, Moriwaki S, Takebe H, Tanaka T, Imamura S.
    Arch Dermatol; 1994 Feb; 130(2):191-7. PubMed ID: 7905727
    [Abstract] [Full Text] [Related]

  • 3. Three nonsense mutations responsible for group A xeroderma pigmentosum.
    Satokata I, Tanaka K, Miura N, Narita M, Mimaki T, Satoh Y, Kondo S, Okada Y.
    Mutat Res; 1992 Mar; 273(2):193-202. PubMed ID: 1372102
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  • 7. Severe neurological abnormalities associated with a mutation in the zinc-finger domain in a group A xeroderma pigmentosum patient.
    Maeda T, Sato K, Minami H, Taguchi H, Yoshikawa K.
    Br J Dermatol; 1994 Oct; 131(4):566-70. PubMed ID: 7947212
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  • 9. Mutations in the XPD gene leading to xeroderma pigmentosum symptoms.
    Kobayashi T, Kuraoka I, Saijo M, Nakatsu Y, Tanaka A, Someda Y, Fukuro S, Tanaka K.
    Hum Mutat; 1997 Oct; 9(4):322-31. PubMed ID: 9101292
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  • 10. Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosum.
    Pawsey SA, Magnus IA, Ramsay CA, Benson PF, Giannelli F.
    Q J Med; 1979 Apr; 48(190):179-210. PubMed ID: 504548
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  • 11. Characterization of a splicing mutation in group A xeroderma pigmentosum.
    Satokata I, Tanaka K, Miura N, Miyamoto I, Satoh Y, Kondo S, Okada Y.
    Proc Natl Acad Sci U S A; 1990 Dec; 87(24):9908-12. PubMed ID: 1702221
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  • 12. Genetic homogeneity of mutational spectrum of group-A xeroderma pigmentosum in Tunisian patients.
    Messaoud O, Ben Rekaya M, Cherif W, Talmoudi F, Boussen H, Mokhtar I, Boubaker S, Amouri A, Abdelhak S, Zghal M.
    Int J Dermatol; 2010 May; 49(5):544-8. PubMed ID: 20534089
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  • 13. Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patients.
    Amr K, Messaoud O, El Darouti M, Abdelhak S, El-Kamah G.
    Gene; 2014 Jan 01; 533(1):52-6. PubMed ID: 24135642
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  • 14. [Xeroderma pigmentosum. A study in 40 Algerian patients].
    Bouadjar B, Aït-Belkacem F, Daya-Grosjean L, Sarasin A, Larbaoui SL, Ferhat R, Cherid MC, Bendissari A, Chouiter A, Bouzid K, Henni T, Hafiz A, Allouache A, Ysmail-Dahlouk M.
    Ann Dermatol Venereol; 1996 Jan 01; 123(5):303-6. PubMed ID: 8761081
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  • 15. Splice site mutations in a xeroderma pigmentosum group A patient with delayed onset of neurological disease.
    States JC, Myrand SP.
    Mutat Res; 1996 Aug 08; 363(3):171-7. PubMed ID: 8765158
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  • 16. Distribution of mutations in the human xeroderma pigmentosum group A gene and their relationships to the functional regions of the DNA damage recognition protein.
    States JC, McDuffie ER, Myrand SP, McDowell M, Cleaver JE.
    Hum Mutat; 1998 Aug 08; 12(2):103-13. PubMed ID: 9671271
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  • 17. Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family.
    Messaoud O, Ben Rekaya M, Kefi R, Chebel S, Boughammoura-Bouatay A, Bel Hadj Ali H, Gouider-Khouja N, Zili J, Frih-Ayed M, Mokhtar I, Abdelhak S, Zghal M.
    Br J Dermatol; 2010 Apr 08; 162(4):883-6. PubMed ID: 20199544
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  • 18. Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain.
    Tanaka K, Miura N, Satokata I, Miyamoto I, Yoshida MC, Satoh Y, Kondo S, Yasui A, Okayama H, Okada Y.
    Nature; 1990 Nov 01; 348(6296):73-6. PubMed ID: 2234061
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  • 19. High prevalence of the point mutation in exon 6 of the xeroderma pigmentosum group A-complementing (XPAC) gene in xeroderma pigmentosum group A patients in Tunisia.
    Nishigori C, Zghal M, Yagi T, Imamura S, Komoun MR, Takebe H.
    Am J Hum Genet; 1993 Nov 01; 53(5):1001-6. PubMed ID: 8105686
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  • 20. Allelic heterogeneity in group A xeroderma pigmentosum.
    Mimaki T, Tanaka K, Okada Y, Minami R, Tachi N, Nagai A, Mino M.
    Acta Neurol Scand; 1992 May 01; 85(5):327-30. PubMed ID: 1621494
    [Abstract] [Full Text] [Related]

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