189 related articles for article (PubMed ID: 28440507)
21. 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]
22. Comparative aspects of the Werner syndrome gene.
Oshima J
In Vivo; 2000; 14(1):165-72. PubMed ID: 10757074
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice.
Aumailley L; Garand C; Dubois MJ; Johnson FB; Marette A; Lebel M
PLoS One; 2015; 10(10):e0140292. PubMed ID: 26447695
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. The spectrum of WRN mutations in Werner syndrome patients.
Huang S; Lee L; Hanson NB; Lenaerts C; Hoehn H; Poot M; Rubin CD; Chen DF; Yang CC; Juch H; Dorn T; Spiegel R; Oral EA; Abid M; Battisti C; Lucci-Cordisco E; Neri G; Steed EH; Kidd A; Isley W; Showalter D; Vittone JL; Konstantinow A; Ring J; Meyer P; Wenger SL; von Herbay A; Wollina U; Schuelke M; Huizenga CR; Leistritz DF; Martin GM; Mian IS; Oshima J
Hum Mutat; 2006 Jun; 27(6):558-67. PubMed ID: 16673358
[TBL] [Abstract][Full Text] [Related]
28. WRN protein as a novel erythroblast immunohistochemical marker with applications for the diagnosis of Werner syndrome.
Sadahira Y; Sugihara T; Fujiwara H; Nishimura H; Suetsugu Y; Takeshita M; Okamura S; Goto M
Virchows Arch; 2015 Mar; 466(3):343-50. PubMed ID: 25503078
[TBL] [Abstract][Full Text] [Related]
29. [Atypical Werner syndrome: Atypical progeroid syndrome: A case report].
Barrios Sanjuanelo A; Muñoz Otero C
An Pediatr (Barc); 2010 Aug; 73(2):94-7. PubMed ID: 20452840
[TBL] [Abstract][Full Text] [Related]
30. A novel WRN mutation identified in a patient with Werner syndrome and acute generalized exanthematous pustulosis.
Kawai T; Hayashi R; Hama N; Shinkuma S; Fujimoto A; Shimomura Y; Abe R
Eur J Dermatol; 2018 Aug; 28(4):553-554. PubMed ID: 29952303
[No Abstract] [Full Text] [Related]
31. Ectopic hTERT expression facilitates reprograming of fibroblasts derived from patients with Werner syndrome as a WS cellular model.
Wang S; Liu Z; Ye Y; Li B; Liu T; Zhang W; Liu GH; Zhang YA; Qu J; Xu D; Chen Z
Cell Death Dis; 2018 Sep; 9(9):923. PubMed ID: 30206203
[TBL] [Abstract][Full Text] [Related]
32. Failure to complement abnormal phenotypes of simian virus 40-transformed Werner syndrome cells by introduction of a normal human chromosome 8.
Kodama S; Kashino G; Suzuki K; Takatsuji T; Okumura Y; Oshimura M; Watanabe M; Barrett JC
Cancer Res; 1998 Nov; 58(22):5188-95. PubMed ID: 9823331
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Mismatch repair in extracts of Werner syndrome cell lines.
Bennett SE; Umar A; Oshima J; Monnat RJ; Kunkel TA
Cancer Res; 1997 Jul; 57(14):2956-60. PubMed ID: 9230208
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Case Report: A novel
Peng H; Wang J; Liu Y; Yang H; Li L; Ma Y; Zhuo H; Jiang H
Front Endocrinol (Lausanne); 2022; 13():918979. PubMed ID: 35909544
[TBL] [Abstract][Full Text] [Related]
37. Preferential expression of an intact WRN gene in Werner syndrome cell lines in which a normal chromosome 8 has been introduced.
Kashino G; Kodama S; Suzuki K; Oshimura M; Watanabe M
Biochem Biophys Res Commun; 2001 Nov; 289(1):111-5. PubMed ID: 11708785
[TBL] [Abstract][Full Text] [Related]
38. Syndrome-causing mutations in Werner syndrome.
Goto M
Biosci Trends; 2008 Aug; 2(4):147-50. PubMed ID: 20103920
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. The Werner syndrome protein: an update.
Oshima J
Bioessays; 2000 Oct; 22(10):894-901. PubMed ID: 10984715
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
