BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 34564935)

  • 21. 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]  

  • 22. Diabetes mellitus coexisted with progeria: a case report of atypical Werner syndrome with novel LMNA mutations and literature review.
    He G; Yan Z; Sun L; Lv Y; Guo W; Gang X; Wang G
    Endocr J; 2019 Nov; 66(11):961-969. PubMed ID: 31270292
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases.
    Lebel M; Monnat RJ
    Ageing Res Rev; 2018 Jan; 41():82-97. PubMed ID: 29146545
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Atypical Werner syndrome: Atypical progeroid syndrome: A case report].
    Barrios Sanjuanelo A; Muñoz Otero C
    An Pediatr (Barc); 2010 Aug; 73(2):94-7. PubMed ID: 20452840
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. The Werner syndrome helicase-nuclease--one protein, many mysteries.
    Fry M
    Sci Aging Knowledge Environ; 2002 Apr; 2002(13):re2. PubMed ID: 14602980
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Possible associations between successful aging and polymorphic markers in the Werner gene region.
    Sild M; Koca C; Bendixen MH; Frederiksen H; McGue M; Kølvraa S; Christensen K; Nexø B
    Ann N Y Acad Sci; 2006 May; 1067():309-10. PubMed ID: 16804003
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

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

  • 30. 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]  

  • 31. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes.
    Maierhofer A; Flunkert J; Oshima J; Martin GM; Poot M; Nanda I; Dittrich M; Müller T; Haaf T
    Aging Cell; 2019 Oct; 18(5):e12995. PubMed ID: 31259468
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Case report: A case of Werner syndrome with compound heterozygous mutations of WRN gene].
    Tamori Y; Takahashi T; Nakajima S; Nishimoto Y; Ohno K; Takemoto M; Yokote K; Kita T; Tsutsumi M
    Nihon Naika Gakkai Zasshi; 2011 Jun; 100(6):1642-4. PubMed ID: 21770289
    [No Abstract]   [Full Text] [Related]  

  • 33. WRN polymorphisms affect expression levels of plasminogen activator inhibitor type 1 in cultured fibroblasts.
    Castro E; Oviedo-Rodríguez V; Angel-Chávez LI
    BMC Cardiovasc Disord; 2008 Feb; 8():5. PubMed ID: 18312663
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Werner Syndrome, aging and cancer.
    Ozgenc A; Loeb LA
    Genome Dyn; 2006; 1():206-217. PubMed ID: 18724062
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Werner syndrome. A prototypical form of segmental progeria.].
    Lessel D; Oshima J; Kubisch C
    Med Genet; 2012 Dec; 24(4):262-267. PubMed ID: 25309043
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Werner Protein Acts as a Coactivator of Nuclear Factor κB (NF-κB) on HIV-1 and Interleukin-8 (IL-8) Promoters.
    Mizutani T; Ishizaka A; Furuichi Y
    J Biol Chem; 2015 Jul; 290(30):18391-9. PubMed ID: 26037922
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes.
    Moser MJ; Bigbee WL; Grant SG; Emond MJ; Langlois RG; Jensen RH; Oshima J; Monnat RJ
    Cancer Res; 2000 May; 60(9):2492-6. PubMed ID: 10811130
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process.
    Opresko PL; Cheng WH; von Kobbe C; Harrigan JA; Bohr VA
    Carcinogenesis; 2003 May; 24(5):791-802. PubMed ID: 12771022
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population.
    Ye L; Miki T; Nakura J; Oshima J; Kamino K; Rakugi H; Ikegami H; Higaki J; Edland SD; Martin GM; Ogihara T
    Am J Med Genet; 1997 Feb; 68(4):494-8. PubMed ID: 9021029
    [TBL] [Abstract][Full Text] [Related]  

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