BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 37573316)

  • 21. Novel mutation identified in the DDB2 gene in patients with xeroderma pigmentosum group-E.
    Karagün E; Eroz R; Gamsızkan M; Baysak S; Eyup Y; Ozcan Y
    Int J Dermatol; 2020 Aug; 59(8):989-996. PubMed ID: 32530099
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Xeroderma pigmentosum in the United kingdom.
    Lehmann AR
    Photochem Photobiol; 2015; 91(2):484-5. PubMed ID: 24943090
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Rare exon 10 deletion in POLH gene in a family with xeroderma pigmentosum variant correlating with protein expression by immunohistochemistry.
    Borroni RG; Diegoli M; Grasso M; Concardi M; Agozzino M; Vignini M; Arbustini E
    G Ital Dermatol Venereol; 2020 Jun; 155(3):349-354. PubMed ID: 32635709
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Xeroderma pigmentosum: low prevalence of germline XPA mutations in a Brazilian XP population.
    Santiago KM; França de Nóbrega A; Rocha RM; Rogatto SR; Achatz MI
    Int J Mol Sci; 2015 Apr; 16(4):8988-96. PubMed ID: 25913378
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Xeroderma pigmentosum variant with multisystem involvement.
    Hessel A; Siegle RJ; Mitchell DL; Cleaver JE
    Arch Dermatol; 1992 Sep; 128(9):1233-7. PubMed ID: 1519938
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Complementation of the DNA repair deficiency in human xeroderma pigmentosum group a and C cells by recombinant adenovirus-mediated gene transfer.
    Muotri AR; Marchetto MC; Zerbini LF; Libermann TA; Ventura AM; Sarasin A; Menck CF
    Hum Gene Ther; 2002 Oct; 13(15):1833-44. PubMed ID: 12396616
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Xeroderma pigmentosum (XP) : A genetic disease sheds light on UV-induced skin cancer].
    Emmert B; Hallier E; Schön MP; Emmert S
    Hautarzt; 2011 Feb; 62(2):91-7. PubMed ID: 21243329
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients.
    Santiago KM; Castro LP; Neto JPD; de Nóbrega AF; Pinto CAL; Ashton-Prolla P; Pinto E Vairo F; de Medeiros PFV; Ribeiro EM; Ribeiro BFR; do Valle FF; Doriqui MJR; Leite CHB; Rocha RM; Moura LMS; Munford V; Galante PAF; Menck CFM; Rogatto SR; Achatz MI
    J Eur Acad Dermatol Venereol; 2020 Oct; 34(10):2392-2401. PubMed ID: 32239545
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Xeroderma pigmentosum].
    Takeuchi S
    Nihon Rinsho; 2000 Jul; 58(7):1496-500. PubMed ID: 10921330
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2).
    Emmert S; Ueda T; Zumsteg U; Weber P; Khan SG; Oh KS; Boyle J; Laspe P; Zachmann K; Boeckmann L; Kuschal C; Bircher A; Kraemer KH
    Exp Dermatol; 2009 Jan; 18(1):64-8. PubMed ID: 18637129
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central Brazil.
    Castro LP; Sahbatou M; Kehdy FSG; Farias AA; Yurchenko AA; de Souza TA; Rosa RCA; Mendes-Junior CT; Borda V; Munford V; Zanardo ÉA; Chehimi SN; Kulikowski LD; Aquino MM; Leal TP; Tarazona-Santos E; Chaibub SC; Gener B; Calmels N; Laugel V; Sarasin A; Menck CFM
    Mutat Res Genet Toxicol Environ Mutagen; 2020 Apr; 852():503164. PubMed ID: 32265042
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A prevalent mutation with founder effect in xeroderma pigmentosum group C from north Africa.
    Soufir N; Ged C; Bourillon A; Austerlitz F; Chemin C; Stary A; Armier J; Pham D; Khadir K; Roume J; Hadj-Rabia S; Bouadjar B; Taieb A; de Verneuil H; Benchiki H; Grandchamp B; Sarasin A
    J Invest Dermatol; 2010 Jun; 130(6):1537-42. PubMed ID: 20054342
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cancer in families with xeroderma pigmentosum.
    Swift M; Chase C
    J Natl Cancer Inst; 1979 Jun; 62(6):1415-21. PubMed ID: 286113
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Validation of XP-C pathogenic variations in archival material from a live XP patient.
    McDaniel LD; Rivera-Begeman A; Doughty AT; Schultz RA; Friedberg EC
    DNA Repair (Amst); 2007 Jan; 6(1):115-20. PubMed ID: 17084680
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Ocular manifestations of xeroderma pigmentosum: long-term follow-up highlights the role of DNA repair in protection from sun damage.
    Brooks BP; Thompson AH; Bishop RJ; Clayton JA; Chan CC; Tsilou ET; Zein WM; Tamura D; Khan SG; Ueda T; Boyle J; Oh KS; Imoto K; Inui H; Moriwaki S; Emmert S; Iliff NT; Bradford P; Digiovanna JJ; Kraemer KH
    Ophthalmology; 2013 Jul; 120(7):1324-36. PubMed ID: 23601806
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular genetic analysis of 16 XP-C patients from Germany: environmental factors predominately contribute to phenotype variations.
    Schäfer A; Hofmann L; Gratchev A; Laspe P; Schubert S; Schürer A; Ohlenbusch A; Tzvetkov M; Hallermann C; Reichrath J; Schön MP; Emmert S
    Exp Dermatol; 2013 Jan; 22(1):24-9. PubMed ID: 23173980
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Xeroderma pigmentosum in four siblings with three different types of malignancies simultaneously in one.
    El-Hayek M; Lestringant GG; Frossard PM
    J Pediatr Hematol Oncol; 2004 Aug; 26(8):473-5. PubMed ID: 15284581
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel missense variant and multiexon deletion causing a delayed presentation of xeroderma pigmentosum, group C.
    Macke EL; Morales-Rosado JA; Gupta A; Schmitz CT; Kruisselbrink T; Lanpher B; Klee EW
    Cold Spring Harb Mol Case Stud; 2020 Aug; 6(4):. PubMed ID: 32843428
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.