159 related articles for article (PubMed ID: 35780059)
1. 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]
2. 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]
3. Werner syndrome presenting as early-onset diabetes: A case report.
Wang X; Liu S; Qin F; Liu Q; Wang Q
J Diabetes Investig; 2022 Mar; 13(3):592-598. PubMed ID: 34564935
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3.
Aggarwal M; Brosh RM
Aging (Albany NY); 2009 Feb; 1(2):219-33. PubMed ID: 20157511
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. A homozygous missense variant in the WRN gene segregating in a family with progressive pulmonary failure with recurrent spontaneous pneumothorax and interstitial lung disease.
Sezer A; Kayhan G; Gursoy TR; Eyuboglu TS; Percin FE
Am J Med Genet A; 2023 Jan; 191(1):220-227. PubMed ID: 36214313
[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. 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]
11. The Drosophila orthologue of progeroid human WRN exonuclease, DmWRNexo, cleaves replication substrates but is inhibited by uracil or abasic sites : analysis of DmWRNexo activity in vitro.
Mason PA; Boubriak I; Robbins T; Lasala R; Saunders R; Cox LS
Age (Dordr); 2013 Jun; 35(3):793-806. PubMed ID: 22562358
[TBL] [Abstract][Full Text] [Related]
12. Uncommon cause of cirrhosis-A case of Werner syndrome with a novel WRN mutation.
Amalnath SD; Sargolzaeiaval F; Oshima J; Baskar D
Indian J Gastroenterol; 2017 Jul; 36(4):323-325. PubMed ID: 28795391
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.
Shen JC; Gray MD; Oshima J; Kamath-Loeb AS; Fry M; Loeb LA
J Biol Chem; 1998 Dec; 273(51):34139-44. PubMed ID: 9852073
[TBL] [Abstract][Full Text] [Related]
16. DNA binding residues in the RQC domain of Werner protein are critical for its catalytic activities.
Tadokoro T; Kulikowicz T; Dawut L; Croteau DL; Bohr VA
Aging (Albany NY); 2012 Jun; 4(6):417-29. PubMed ID: 22713343
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. A Novel Variant in the WRN Gene Detected in a Case of Early-Onset Severe Insulin Resistance Displaying Some but Not All Hallmarks of Progeroid Werner Syndrome.
Spira D; Herbst S; Schwartzmann S; Dutrannoy V; Steinhagen-Thiessen E; Demuth I; Maurer L; Mai K; Spranger J; Mundlos S; Bobbert T
Diabetes Care; 2024 May; 47(5):798-802. PubMed ID: 38277397
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
