BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 8105686)

  • 1. 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; 53(5):1001-6. PubMed ID: 8105686
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Compound heterozygosity for the Xeroderma pigmentosum complementation group A gene associated with a mild phenotype.
    Negishi I; Kato G; Moriwaki S; Ishikawa O
    Eur J Dermatol; 2002; 12(6):536-9. PubMed ID: 12459522
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Correlation of the clinical manifestations and gene mutations of Japanese xeroderma pigmentosum group A patients.
    Kondoh M; Ueda M; Ichihashi M
    Br J Dermatol; 1995 Oct; 133(4):579-85. PubMed ID: 7577588
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Aberrant splicing and truncated-protein expression due to a newly identified XPA gene mutation.
    Sato M; Nishigori C; Yagi T; Takebe H
    Mutat Res; 1996 Feb; 362(2):199-208. PubMed ID: 8596539
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of splicing mutations of the last nucleotides of exons, a nonsense mutation, and a missense mutation of the XPAC gene as causes of group A xeroderma pigmentosum.
    Satokata I; Tanaka K; Yuba S; Okada Y
    Mutat Res; 1992 Mar; 273(2):203-12. PubMed ID: 1372103
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 12(2):103-13. PubMed ID: 9671271
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular basis of group A xeroderma pigmentosum: a missense mutation and two deletions located in a zinc finger consensus sequence of the XPAC gene.
    Satokata I; Tanaka K; Okada Y
    Hum Genet; 1992 Mar; 88(6):603-7. PubMed ID: 1339397
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. PCR-RFLP analysis as an aid to genetic counseling of families of Japanese patients with group A xeroderma pigmentosum.
    Maeda T; Sato K; Minami H; Taguchi H; Yoshikawa K
    J Invest Dermatol; 1997 Sep; 109(3):306-9. PubMed ID: 9284095
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.
    Messaoud O; Rekaya MB; Ouragini H; Benfadhel S; Azaiez H; Kefi R; Gouider-Khouja N; Mokhtar I; Amouri A; Boubaker MS; Zghal M; Abdelhak S
    Arch Dermatol Res; 2012 Mar; 304(2):171-6. PubMed ID: 22081045
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 125(2):244-6. PubMed ID: 16098033
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 85(5):327-30. PubMed ID: 1621494
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 150(6):1190-3. PubMed ID: 15214909
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 533(1):52-6. PubMed ID: 24135642
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnosis of Xeroderma Pigmentosum Groups A and C by Detection of Two Prevalent Mutations in West Algerian Population: A Rapid Genotyping Tool for the Frequent XPC Mutation c.1643_1644delTG.
    Bensenouci S; Louhibi L; De Verneuil H; Mahmoudi K; Saidi-Mehtar N
    Biomed Res Int; 2016; 2016():2180946. PubMed ID: 27413738
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.