BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

301 related articles for article (PubMed ID: 23524889)

  • 1. Werner syndrome: a changing pattern of clinical manifestations in Japan (1917~2008).
    Goto M; Ishikawa Y; Sugimoto M; Furuichi Y
    Biosci Trends; 2013 Feb; 7(1):13-22. PubMed ID: 23524889
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.
    Muftuoglu M; Oshima J; von Kobbe C; Cheng WH; Leistritz DF; Bohr VA
    Hum Genet; 2008 Nov; 124(4):369-77. PubMed ID: 18810497
    [TBL] [Abstract][Full Text] [Related]  

  • 3. WRN at telomeres: implications for aging and cancer.
    Multani AS; Chang S
    J Cell Sci; 2007 Mar; 120(Pt 5):713-21. PubMed ID: 17314245
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel mutation of the WRN gene in a Chinese patient with Werner syndrome.
    Zhao N; Hao F; Qu T; Zuo YG; Wang BX
    Clin Exp Dermatol; 2008 May; 33(3):278-81. PubMed ID: 18205852
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Syndrome-causing mutations in Werner syndrome.
    Goto M
    Biosci Trends; 2008 Aug; 2(4):147-50. PubMed ID: 20103920
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Werner's Syndrome RecQ helicase/exonuclease at the nexus of cancer and aging.
    Chun SG; Shaeffer DS; Bryant-Greenwood PK
    Hawaii Med J; 2011 Mar; 70(3):52-5. PubMed ID: 21365542
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [Utilization of Werner syndrome mouse model in studying premature aging and tumor].
    Jia ST; Yang SH; Luo Y
    Yi Chuan; 2009 Aug; 31(8):785-90. PubMed ID: 19689938
    [TBL] [Abstract][Full Text] [Related]  

  • 9. First Japanese case of atypical progeroid syndrome/atypical Werner syndrome with heterozygous LMNA mutation.
    Motegi S; Yokoyama Y; Uchiyama A; Ogino S; Takeuchi Y; Yamada K; Hattori T; Hashizume H; Ishikawa Y; Goto M; Ishikawa O
    J Dermatol; 2014 Dec; 41(12):1047-52. PubMed ID: 25327215
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Werner syndrome as a hereditary risk factor for exocrine pancreatic cancer: potential role of WRN in pancreatic tumorigenesis and patient-tailored therapy.
    Chun SG; Yee NS
    Cancer Biol Ther; 2010 Sep; 10(5):430-7. PubMed ID: 20657174
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.
    Oshima J; Hisama FM
    Gerontology; 2014; 60(3):239-46. PubMed ID: 24401204
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Telomere dysfunction as a cause of genomic instability in Werner syndrome.
    Crabbe L; Jauch A; Naeger CM; Holtgreve-Grez H; Karlseder J
    Proc Natl Acad Sci U S A; 2007 Feb; 104(7):2205-10. PubMed ID: 17284601
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Telomere ResQue and preservation--roles for the Werner syndrome protein and other RecQ helicases.
    Opresko PL
    Mech Ageing Dev; 2008; 129(1-2):79-90. PubMed ID: 18054793
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lack of amyloid plaque formation in the central nervous system of a patient with Werner syndrome.
    Mori H; Tomiyama T; Maeda N; Ozawa K; Wakasa K
    Neuropathology; 2003 Mar; 23(1):51-6. PubMed ID: 12722926
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Role of Werner syndrome gene product helicase in carcinogenesis and in resistance to genotoxins by cancer cells.
    Futami K; Ishikawa Y; Goto M; Furuichi Y; Sugimoto M
    Cancer Sci; 2008 May; 99(5):843-8. PubMed ID: 18312465
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Werner syndrome protein: functions in the response to DNA damage and replication stress in S-phase.
    Cheng WH; Muftuoglu M; Bohr VA
    Exp Gerontol; 2007 Sep; 42(9):871-8. PubMed ID: 17587522
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Werner syndrome: clinical evaluation of two cases and a novel mutation.
    Mansur AT; Elçioglu NH; Demirci GT
    Genet Couns; 2014; 25(2):119-27. PubMed ID: 25059010
    [TBL] [Abstract][Full Text] [Related]  

  • 18. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.
    Friedrich K; Lee L; Leistritz DF; Nürnberg G; Saha B; Hisama FM; Eyman DK; Lessel D; Nürnberg P; Li C; Garcia-F-Villalta MJ; Kets CM; Schmidtke J; Cruz VT; Van den Akker PC; Boak J; Peter D; Compoginis G; Cefle K; Ozturk S; López N; Wessel T; Poot M; Ippel PF; Groff-Kellermann B; Hoehn H; Martin GM; Kubisch C; Oshima J
    Hum Genet; 2010 Jul; 128(1):103-11. PubMed ID: 20443122
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Premature aging syndrome gene WRN genetically interacts with a topoisomerase.
    Aggarwal M; Brosh RM
    Cell Cycle; 2009 Jul; 8(14):2143. PubMed ID: 19587535
    [No Abstract]   [Full Text] [Related]  

  • 20. [Werner syndrome].
    Goto M; Ishikawa Y
    Nihon Rinsho; 2000 Jul; 58(7):1490-5. PubMed ID: 10921329
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.