BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Skin cancer AND WRN, RECQL2, 7486, ENSG00000165392, Q14191, RECQ3
23 results:

  • 1. The identification of a novel mutation (p.I223fs) in wrn associated with Werner syndrome.
    Wu J; Pan S; Lin W; Wen J; Lu R; Chen G
    Endocrine; 2024 Apr; 84(1):92-96. PubMed ID: 37856055
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Research on Werner Syndrome: Trends from Past to Present and Future Prospects.
    Tsuge K; Shimamoto A
    Genes (Basel); 2022 Oct; 13(10):. PubMed ID: 36292687
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Dyslipidemia in Patients with Xanthelasma Palpebrarum Visiting the Department of Dermatology of a Tertiary Care Centre: A Descriptive Cross-sectional Study.
    Rai A; Karki S; Prasad Sah S; Narayan Kamat L; Pradhan M
    JNMA J Nepal Med Assoc; 2022 Jun; 60(250):529-532. PubMed ID: 35690977
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families.
    Fidalgo F; Torrezan GT; Sá BCS; Barros BDF; Moredo LF; Valieris R; de Souza SJ; Duprat JP; Krepischi ACV; Carraro DM
    PLoS One; 2022; 17(1):e0262419. PubMed ID: 35085295
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Severe metabolic disorders coexisting with Werner syndrome: a case report.
    Li H; Yang M; Shen H; Wang S; Cai H
    Endocr J; 2021 Mar; 68(3):261-267. PubMed ID: 33087645
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Oral squamous cell carcinoma arising in a patient with Werner syndrome.
    Kuribayashi N; Uchida D; Hamasaki Y; Kawamata H
    Int J Oral Maxillofac Surg; 2019 Nov; 48(11):1394-1397. PubMed ID: 31235391
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Do you know this syndrome? Werner syndrome.
    Bilgiç Ö
    An Bras Dermatol; 2017; 92(2):271-272. PubMed ID: 28538897
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. SNEV
    Khan A; Dellago H; Terlecki-Zaniewicz L; Karbiener M; Weilner S; Hildner F; Steininger V; Gabriel C; Mück C; Jansen-Dürr P; Hacobian A; Scheideler M; Grillari-Voglauer R; Schosserer M; Grillari J
    Stem Cell Reports; 2017 Jan; 8(1):21-29. PubMed ID: 28041875
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. Investigation of Werner protein as an early DNA damage response in actinic keratosis, Bowen disease and squamous cell carcinoma.
    Cha HJ; Lee DB; Jung HN; Choi YS; Suh HS
    Clin Exp Dermatol; 2015 Jul; 40(5):564-9. PubMed ID: 25545408
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey.
    Takemoto M; Mori S; Kuzuya M; Yoshimoto S; Shimamoto A; Igarashi M; Tanaka Y; Miki T; Yokote K
    Geriatr Gerontol Int; 2013 Apr; 13(2):475-81. PubMed ID: 22817610
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. cancer risk with tumor necrosis factor alpha (TNF) inhibitors: meta-analysis of randomized controlled trials of adalimumab, etanercept, and infliximab using patient level data.
    Askling J; Fahrbach K; Nordstrom B; Ross S; Schmid CH; Symmons D
    Pharmacoepidemiol Drug Saf; 2011 Feb; 20(2):119-30. PubMed ID: 21254282
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. Telomere sister chromatid exchange and the process of aging.
    Blagoev KB; Goodwin EH; Bailey SM
    Aging (Albany NY); 2010 Oct; 2(10):727-30. PubMed ID: 20952810
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. Identification of modifier genes for cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations.
    Yang XR; Pfeiffer RM; Wheeler W; Yeager M; Chanock S; Tucker MA; Goldstein AM
    Int J Cancer; 2009 Dec; 125(12):2912-7. PubMed ID: 19626699
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. Bloom's syndrome workshop focuses on the functional specificities of RecQ helicases.
    Ellis NA; Sander M; Harris CC; Bohr VA
    Mech Ageing Dev; 2008 Nov; 129(11):681-91. PubMed ID: 19238688
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents.
    Cabral RE; Queille S; Bodemer C; de Prost Y; Neto JB; Sarasin A; Daya-Grosjean L
    Mutat Res; 2008 Aug; 643(1-2):41-7. PubMed ID: 18616953
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. Contributions of DNA interstrand cross-links to aging of cells and organisms.
    Grillari J; Katinger H; Voglauer R
    Nucleic Acids Res; 2007; 35(22):7566-76. PubMed ID: 18083760
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. [Musculoskeletal complications of Werner's syndrome].
    Kluger N; Aractingi S; Aboukrat P; Vanderlinden I; Guillot B; Bessis D
    Ann Dermatol Venereol; 2007 Feb; 134(2):143-7. PubMed ID: 17375010
    [TBL] [Abstract] [Full Text] [Related]  

  • 18. [Werner's syndrome (adult onset progeria)].
    Kluger N; Bessis D; Uhrhammer N; Guillot B; Aractingi S
    Ann Dermatol Venereol; 2007 Feb; 134(2):140-2. PubMed ID: 17375009
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. Werner syndrome and mutations of the wrn and LMNA genes in France.
    Uhrhammer NA; Lafarge L; Dos Santos L; Domaszewska A; Lange M; Yang Y; Aractingi S; Bessis D; Bignon YJ
    Hum Mutat; 2006 Jul; 27(7):718-9. PubMed ID: 16786514
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. A case of Werner syndrome with three primary lesions of malignant melanoma.
    Shibuya H; Kato A; Kai N; Fujiwara S; Goto M
    J Dermatol; 2005 Sep; 32(9):737-44. PubMed ID: 16361718
    [TBL] [Abstract] [Full Text] [Related]  


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