These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 8105118)

  • 41. [DNA repair defect in xeroderma pigmentosum].
    Tanaka K
    Gan To Kagaku Ryoho; 1989 Mar; 16(3 Pt 2):473-80. PubMed ID: 2650628
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Xeroderma pigmentosum patients belonging to complementation group F and efficient liquid-holding recovery of ultraviolet damage.
    Nishigori C; Fujisawa H; Uyeno K; Kawaguchi T; Takebe H
    Photodermatol Photoimmunol Photomed; 1991 Aug; 8(4):146-50. PubMed ID: 1814424
    [TBL] [Abstract][Full Text] [Related]  

  • 43. High mutation frequency in ras genes of skin tumors isolated from DNA repair deficient xeroderma pigmentosum patients.
    Daya-Grosjean L; Robert C; Drougard C; Suarez H; Sarasin A
    Cancer Res; 1993 Apr; 53(7):1625-9. PubMed ID: 8453633
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Truncated XPA protein detected in atypical group A xeroderma pigmentosum.
    Mimaki T; Nitta M; Saijo M; Tachi N; Minami R; Tanaka K
    Acta Paediatr; 1996 Apr; 85(4):511-3. PubMed ID: 8740317
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Compound heterozygous group A xeroderma pigmentosum patient with a novel mutation and an inherited reciprocal translocation.
    Maeda T; Sato K; Tanaka T; Minami H; Taguchi H; Mimaki T; Yoshikawa K
    Br J Dermatol; 2000 Jul; 143(1):174-9. PubMed ID: 10886156
    [TBL] [Abstract][Full Text] [Related]  

  • 46. DNA-based prenatal carrier detection for group A xeroderma pigmentosum in a chorionic villus sample.
    Matsumoto N; Saito N; Harada N; Tanaka K; Niikawa N
    Prenat Diagn; 1995 Jul; 15(7):675-7. PubMed ID: 8532631
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia.
    Khan SG; Levy HL; Legerski R; Quackenbush E; Reardon JT; Emmert S; Sancar A; Li L; Schneider TD; Cleaver JE; Kraemer KH
    J Invest Dermatol; 1998 Nov; 111(5):791-6. PubMed ID: 9804340
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Genotype-phenotype correlation of xeroderma pigmentosum in a Chinese Han population.
    Sun Z; Zhang J; Guo Y; Ni C; Liang J; Cheng R; Li M; Yao Z
    Br J Dermatol; 2015 Apr; 172(4):1096-102. PubMed ID: 25256075
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. Identification and characterization of xpac protein, the gene product of the human XPAC (xeroderma pigmentosum group A complementing) gene.
    Miura N; Miyamoto I; Asahina H; Satokata I; Tanaka K; Okada Y
    J Biol Chem; 1991 Oct; 266(29):19786-9. PubMed ID: 1918083
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A 10-year follow-up of a child with mild case of xeroderma pigmentosum complementation group D diagnosed by whole-genome sequencing.
    Ono R; Masaki T; Mayca Pozo F; Nakazawa Y; Swagemakers SM; Nakano E; Sakai W; Takeuchi S; Kanda F; Ogi T; van der Spek PJ; Sugasawa K; Nishigori C
    Photodermatol Photoimmunol Photomed; 2016 Jul; 32(4):174-80. PubMed ID: 26993158
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Carrier frequency of the recurrent mutation c.1643_1644delTG in the XPC gene and birth prevalence of the xeroderma pigmentosum in Morocco.
    Doubaj Y; Laarabi FZ; Elalaoui SC; Barkat A; Sefiani A
    J Dermatol; 2012 Apr; 39(4):382-4. PubMed ID: 22211393
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A novel mutation in the XPA gene results in two truncated protein variants and leads to a severe XP/neurological symptoms phenotype.
    Lehmann J; Schubert S; Schäfer A; Laspe P; Haenssle HA; Ohlenbusch A; Gratchev A; Emmert S
    J Eur Acad Dermatol Venereol; 2015 Dec; 29(12):2479-82. PubMed ID: 25393472
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Chronological difference in walking impairment among Japanese group A xeroderma pigmentosum (XP-A) patients with various combinations of mutation sites.
    Maeda T; Sato K; Minami H; Taguchi H; Yoshikawa K
    Clin Genet; 1995 Nov; 48(5):225-31. PubMed ID: 8825598
    [TBL] [Abstract][Full Text] [Related]  

  • 55. An XPA gene splicing mutation resulting in trace protein expression in an elderly patient with xeroderma pigmentosum group A without neurological abnormalities.
    Takahashi Y; Endo Y; Kusaka-Kikushima A; Nakamaura S; Nakazawa Y; Ogi T; Uryu M; Tsuji G; Furue M; Moriwaki S
    Br J Dermatol; 2017 Jul; 177(1):253-257. PubMed ID: 27603812
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Clinical profile and mutation analysis of xeroderma pigmentosum in Indian patients.
    Tamhankar PM; Iyer SV; Ravindran S; Gupta N; Kabra M; Nayak C; Kura M; Sanghavi S; Joshi R; Chennuri VS; Khopkar U
    Indian J Dermatol Venereol Leprol; 2015; 81(1):16-22. PubMed ID: 25566891
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Patients with xeroderma pigmentosum complementation groups C, E and V do not have abnormal sunburn reactions.
    Sethi M; Lehmann AR; Fawcett H; Stefanini M; Jaspers N; Mullard K; Turner S; Robson A; McGibbon D; Sarkany R; Fassihi H
    Br J Dermatol; 2013 Dec; 169(6):1279-87. PubMed ID: 23889214
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Molecular studies of Japanese patients with group A xeroderma pigmentosum using polymerase chain reaction and restriction fragment length polymorphism and nonradioactive single strand conformation polymorphism analyses.
    Sumitani S; Ishikawa Y; Ishikawa Y; Minami R
    J Child Neurol; 1999 Mar; 14(3):168-72. PubMed ID: 10190268
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A single-site mutation in the XPAC gene alters photoproduct recognition.
    McDowell ML; Nguyen T; Cleaver JE
    Mutagenesis; 1993 Mar; 8(2):155-61. PubMed ID: 8464385
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced XPC mRNA levels that correlate with cancer risk.
    Khan SG; Metin A; Gozukara E; Inui H; Shahlavi T; Muniz-Medina V; Baker CC; Ueda T; Aiken JR; Schneider TD; Kraemer KH
    Hum Mol Genet; 2004 Feb; 13(3):343-52. PubMed ID: 14662655
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.