BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 8722214)

  • 1. Excess of rare cancers in Werner syndrome (adult progeria).
    Goto M; Miller RW; Ishikawa Y; Sugano H
    Cancer Epidemiol Biomarkers Prev; 1996 Apr; 5(4):239-46. PubMed ID: 8722214
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
    Piver MS
    Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A genetic analysis of the Werner syndrome region on human chromosome 8p.
    Thomas W; Rubenstein M; Goto M; Drayna D
    Genomics; 1993 Jun; 16(3):685-90. PubMed ID: 8325642
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mapping.
    Ye L; Nakura J; Mitsuda N; Fujioka Y; Kamino K; Ohta T; Jinno Y; Niikawa N; Miki T; Ogihara T
    Genomics; 1995 Aug; 28(3):566-9. PubMed ID: 7490095
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Meningioma arising in Werner syndrome confirmed by mutation analysis.
    Nakamura Y; Shimizu T; Ohigashi Y; Itou N; Ishikawa Y
    J Clin Neurosci; 2005 May; 12(4):503-6. PubMed ID: 15925797
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, and atherosclerosis.
    Castro E; Edland SD; Lee L; Ogburn CE; Deeb SS; Brown G; Panduro A; Riestra R; Tilvis R; Louhija J; Penttinen R; Erkkola R; Wang L; Martin GM; Oshima J
    Am J Med Genet; 2000 Dec; 95(4):374-80. PubMed ID: 11186893
    [TBL] [Abstract][Full Text] [Related]  

  • 7. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.
    Yokote K; Chanprasert S; Lee L; Eirich K; Takemoto M; Watanabe A; Koizumi N; Lessel D; Mori T; Hisama FM; Ladd PD; Angle B; Baris H; Cefle K; Palanduz S; Ozturk S; Chateau A; Deguchi K; Easwar TK; Federico A; Fox A; Grebe TA; Hay B; Nampoothiri S; Seiter K; Streeten E; PiƱa-Aguilar RE; Poke G; Poot M; Posmyk R; Martin GM; Kubisch C; Schindler D; Oshima J
    Hum Mutat; 2017 Jan; 38(1):7-15. PubMed ID: 27667302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tumorigenic effect of nonfunctional p53 or p21 in mice mutant in the Werner syndrome helicase.
    Lebel M; Cardiff RD; Leder P
    Cancer Res; 2001 Mar; 61(5):1816-9. PubMed ID: 11280729
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recent Trends in WRN Gene Mutation Patterns in Individuals with Werner Syndrome.
    Yamaga M; Takemoto M; Takada-Watanabe A; Koizumi N; Kitamoto T; Sakamoto K; Ishikawa T; Koshizaka M; Maezawa Y; Yokote K
    J Am Geriatr Soc; 2017 Aug; 65(8):1853-1856. PubMed ID: 28394436
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular and epidemiological studies of Werner syndrome in the Japanese population.
    Miki T; Nakura J; Ye L; Mitsuda N; Morishima A; Sato N; Kamino K; Ogihara T
    Mech Ageing Dev; 1997 Dec; 98(3):255-65. PubMed ID: 9352494
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians.
    Castro E; Ogburn CE; Hunt KE; Tilvis R; Louhija J; Penttinen R; Erkkola R; Panduro A; Riestra R; Piussan C; Deeb SS; Wang L; Edland SD; Martin GM; Oshima J
    Am J Med Genet; 1999 Feb; 82(5):399-403. PubMed ID: 10069711
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Meningioma in a patient with Werner syndrome.
    Pattankar S; Churi O; Misra BK
    Neurol India; 2020; 68(2):483-486. PubMed ID: 32415031
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Atypical osteosarcomas in Werner Syndrome (adult progeria).
    Ishikawa Y; Miller RW; Machinami R; Sugano H; Goto M
    Jpn J Cancer Res; 2000 Dec; 91(12):1345-9. PubMed ID: 11123436
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Secular trends towards delayed onsets of pathologies and prolonged longevities in Japanese patients with Werner syndrome.
    Goto M; Matsuura M
    Biosci Trends; 2008 Apr; 2(2):81-7. PubMed ID: 20103906
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Molecular epidemiology of breast cancers in northern and southern Japan: the frequency, clustering, and patterns of p53 gene mutations differ among these two low-risk populations.
    Blaszyk H; Hartmann A; Tamura Y; Saitoh S; Cunningham JM; McGovern RM; Schroeder JJ; Schaid DJ; Ii K; Monden Y; Morimoto T; Komaki K; Sasa M; Hirata K; Okazaki M; Kovach JS; Sommer SS
    Oncogene; 1996 Nov; 13(10):2159-66. PubMed ID: 8950983
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Werner syndrome protein is a DNA helicase.
    Gray MD; Shen JC; Kamath-Loeb AS; Blank A; Sopher BL; Martin GM; Oshima J; Loeb LA
    Nat Genet; 1997 Sep; 17(1):100-3. PubMed ID: 9288107
    [TBL] [Abstract][Full Text] [Related]  

  • 18. LMNA mutations in progeroid syndromes.
    Huang S; Kennedy BK; Oshima J
    Novartis Found Symp; 2005; 264():197-202; discussion 202-7, 227-30. PubMed ID: 15773755
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Werner syndrome gene and global sequence variation.
    Passarino G; Shen P; Van Kirk JB; Lin AA; De Benedictis G; Cavalli Sforza LL; Oefner PJ; Underhill PA
    Genomics; 2001 Jan; 71(1):118-22. PubMed ID: 11161804
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race.
    Ishikawa Y; Sugano H; Matsumoto T; Furuichi Y; Miller RW; Goto M
    Cancer; 1999 Mar; 85(6):1345-52. PubMed ID: 10189141
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.