These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 17478382)

  • 1. Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster.
    Masala MV; Scapaticci S; Olivieri C; Pirodda C; Montesu MA; Cuccuru MA; Pruneddu S; Danesino C; Cerimele D
    Eur J Dermatol; 2007; 17(3):213-6. PubMed ID: 17478382
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Genetic analyses of two cases of Werner's syndrome.
    Sogabe Y; Yasuda M; Yokoyama Y; Tamura A; Negishi I; Ohnishi K; Shinozaki T; Ishikawa O
    Eur J Dermatol; 2004; 14(6):379-82. PubMed ID: 15564200
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Comparative aspects of the Werner syndrome gene.
    Oshima J
    In Vivo; 2000; 14(1):165-72. PubMed ID: 10757074
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Teaching neuroimages: a prematurely aging patient presenting with severe leukoaraiosis and stroke.
    Seixas JC; Pedroso JL; Fukuda TG; de Figueiredo MM; Baiense RF; Yared JH; Ferraz HB; Barsottini OG
    Neurology; 2012 May; 78(18):e113-4. PubMed ID: 22547774
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

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

  • 12. LMNA mutations in atypical Werner's syndrome.
    Chen L; Lee L; Kudlow BA; Dos Santos HG; Sletvold O; Shafeghati Y; Botha EG; Garg A; Hanson NB; Martin GM; Mian IS; Kennedy BK; Oshima J
    Lancet; 2003 Aug; 362(9382):440-5. PubMed ID: 12927431
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of Werner syndrome without metabolic abnormality: implications for the early pathophysiology.
    Takada-Watanabe A; Yokote K; Takemoto M; Fujimoto M; Irisuna H; Honjo S; Futami K; Furuichi Y; Saito Y
    Geriatr Gerontol Int; 2012 Jan; 12(1):140-6. PubMed ID: 22188495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency.
    Cerimele D; Cottoni F; Scappaticci S; Rabbiosi G; Borroni G; Sanna E; Zei G; Fraccaro M
    Hum Genet; 1982; 62(1):25-30. PubMed ID: 7152524
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Werner's syndrome: seven cases in one family.
    Rabbiosi G; Borroni G
    Dermatologica; 1979; 158(5):355-60. PubMed ID: 437224
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer. Mutations in brief no. 136. Online.
    Vidal V; Bay JO; Champomier F; Grancho M; Beauville L; Glowaczower C; Lemery D; Ferrara M; Bignon YJ
    Hum Mutat; 1998; 11(5):413-4. PubMed ID: 10206685
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Werner Syndrome as an example of inflamm-aging: possible therapeutic opportunities for a progeroid syndrome?
    Davis T; Kipling D
    Rejuvenation Res; 2006; 9(3):402-7. PubMed ID: 16859481
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Positional cloning of the Werner's syndrome gene.
    Yu CE; Oshima J; Fu YH; Wijsman EM; Hisama F; Alisch R; Matthews S; Nakura J; Miki T; Ouais S; Martin GM; Mulligan J; Schellenberg GD
    Science; 1996 Apr; 272(5259):258-62. PubMed ID: 8602509
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnosis of Werner syndrome by immunoblot analysis.
    Shimizu T; Tateishi Y; Furuichi Y; Sugimoto M; Kawabe T; Matsumoto T; Shimizu H
    Clin Exp Dermatol; 2002 Mar; 27(2):157-9. PubMed ID: 11952711
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.