176 related articles for article (PubMed ID: 35037378)
1. 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]
2. Severe metabolic disorders coexisting with Werner syndrome: a case report.
Li H; Yang M; Shen H; Wang S; Cai H
Endocr J; 2021 Mar; 68(3):261-267. PubMed ID: 33087645
[TBL] [Abstract][Full Text] [Related]
3. The identification of a novel mutation (p.I223fs) in WRN associated with Werner syndrome.
Wu J; Pan S; Lin W; Wen J; Lu R; Chen G
Endocrine; 2024 Apr; 84(1):92-96. PubMed ID: 37856055
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
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. 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]
10. Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C.
Matsumoto N; Ohta Y; Deguchi K; Kishida M; Sato K; Shang J; Takemoto M; Hishikawa N; Yamashita T; Watanabe A; Yokote K; Takemoto M; Oshima J; Abe K
Intern Med; 2019 Apr; 58(7):1033-1036. PubMed ID: 30568144
[TBL] [Abstract][Full Text] [Related]
11. Research on Werner Syndrome: Trends from Past to Present and Future Prospects.
Tsuge K; Shimamoto A
Genes (Basel); 2022 Oct; 13(10):. PubMed ID: 36292687
[TBL] [Abstract][Full Text] [Related]
12. Partial lipodystrophy, severe dyslipidaemia and insulin resistant diabetes as early signs of Werner syndrome.
Atallah I; McCormick D; Good JM; Barigou M; Fraga M; Sempoux C; Superti-Furga A; Semple RK; Tran C
J Clin Lipidol; 2022; 16(5):583-590. PubMed ID: 35780059
[TBL] [Abstract][Full Text] [Related]
13. A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome.
Wu PF; Jin JY; Li JJ; He JQ; Fan LL; Jin M; Huang H; Xia K; Tang JY; Xiang R
Mol Med Rep; 2017 Jun; 15(6):3735-3738. PubMed ID: 28440507
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. [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]
17. Bloom's syndrome: Why not premature aging?: A comparison of the BLM and WRN helicases.
de Renty C; Ellis NA
Ageing Res Rev; 2017 Jan; 33():36-51. PubMed ID: 27238185
[TBL] [Abstract][Full Text] [Related]
18. Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey.
Takemoto M; Mori S; Kuzuya M; Yoshimoto S; Shimamoto A; Igarashi M; Tanaka Y; Miki T; Yokote K
Geriatr Gerontol Int; 2013 Apr; 13(2):475-81. PubMed ID: 22817610
[TBL] [Abstract][Full Text] [Related]
19. 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; Piña-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]
20. 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]
[Next] [New Search]