BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 36396328)

  • 1. Adult progeria: a new mutation in the WRN gene.
    Rocha ML; Chicharo AT; Sequeira G; Teixeira V
    BMJ Case Rep; 2022 Nov; 15(11):. PubMed ID: 36396328
    [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. 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]  

  • 4. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions.
    Oshima J; Sidorova JM; Monnat RJ
    Ageing Res Rev; 2017 Jan; 33():105-114. PubMed ID: 26993153
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. 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]  

  • 9. Functional deficit associated with a missense Werner syndrome mutation.
    Tadokoro T; Rybanska-Spaeder I; Kulikowicz T; Dawut L; Oshima J; Croteau DL; Bohr VA
    DNA Repair (Amst); 2013 Jun; 12(6):414-21. PubMed ID: 23583337
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.
    Donadille B; D'Anella P; Auclair M; Uhrhammer N; Sorel M; Grigorescu R; Ouzounian S; Cambonie G; Boulot P; Laforêt P; Carbonne B; Christin-Maitre S; Bignon YJ; Vigouroux C
    Orphanet J Rare Dis; 2013 Jul; 8():106. PubMed ID: 23849162
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Generation of disease-specific and CRISPR/Cas9-mediated gene-corrected iPS cells from a patient with adult progeria Werner syndrome.
    Kato H; Maezawa Y; Ouchi Y; Takayama N; Sone M; Sone K; Takada-Watanabe A; Tsujimura K; Koshizaka M; Nagasawa S; Saitoh H; Ohtaka M; Nakanishi M; Tahara H; Shimamoto A; Iwama A; Eto K; Yokote K
    Stem Cell Res; 2021 May; 53():102360. PubMed ID: 34087989
    [TBL] [Abstract][Full Text] [Related]  

  • 17. WRN mutations in Werner syndrome.
    Moser MJ; Oshima J; Monnat RJ
    Hum Mutat; 1999; 13(4):271-9. PubMed ID: 10220139
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay.
    Müller FB; Tsianakas A; Kuwert C; Korge BP; Hunzelmann N
    Br J Dermatol; 2005 May; 152(5):1030-2. PubMed ID: 15888165
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Werner syndrome in a Lebanese family.
    Jaafar B; Nasrallah M; Sievers B; Oshima J; Lessel D
    Am J Med Genet A; 2022 May; 188(5):1630-1634. PubMed ID: 35037378
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 9.