232 related articles for article (PubMed ID: 8722214)
21. 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]
22. [Genetic analysis of Werner syndrome in a family].
Morishima A; Mitsuda N; Nakura J; Kamino K; Sato N; Miki T; Ogihara T
Nihon Ronen Igakkai Zasshi; 1995 Dec; 32(12):817-21. PubMed ID: 8865743
[TBL] [Abstract][Full Text] [Related]
23. Cancer and non-cancer effects in Japanese atomic bomb survivors.
Little MP
J Radiol Prot; 2009 Jun; 29(2A):A43-59. PubMed ID: 19454804
[TBL] [Abstract][Full Text] [Related]
24. A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Yu CE; Oshima J; Hisama FM; Matthews S; Trask BJ; Schellenberg GD
Genomics; 1996 Aug; 35(3):431-40. PubMed ID: 8812476
[TBL] [Abstract][Full Text] [Related]
25. Papillon-Lefèvre syndrome and malignant melanoma. A high incidence of melanoma development in Japanese palmoplantar keratoderma patients.
Nakajima K; Nakano H; Takiyoshi N; Rokunohe A; Ikenaga S; Aizu T; Kaneko T; Mitsuhashi Y; Sawamura D
Dermatology; 2008; 217(1):58-62. PubMed ID: 18401176
[TBL] [Abstract][Full Text] [Related]
26. The Werner syndrome protein at the crossroads of DNA repair and apoptosis.
Comai L; Li B
Mech Ageing Dev; 2004 Aug; 125(8):521-8. PubMed ID: 15336909
[TBL] [Abstract][Full Text] [Related]
27. Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.
Yu CE; Oshima J; Goddard KA; Miki T; Nakura J; Ogihara T; Poot M; Hoehn H; Fraccaro M; Piussan C
Am J Hum Genet; 1994 Aug; 55(2):356-64. PubMed ID: 8037212
[TBL] [Abstract][Full Text] [Related]
28. Spectrum and risk of neoplasia in Werner syndrome: a systematic review.
Lauper JM; Krause A; Vaughan TL; Monnat RJ
PLoS One; 2013; 8(4):e59709. PubMed ID: 23573208
[TBL] [Abstract][Full Text] [Related]
29. Corneal dystrophies in Japan.
Fujiki K; Nakayasu K; Kanai A
J Hum Genet; 2001; 46(8):431-5. PubMed ID: 11501939
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.
Goddard KA; Yu CE; Oshima J; Miki T; Nakura J; Piussan C; Martin GM; Schellenberg GD; Wijsman EM
Am J Hum Genet; 1996 Jun; 58(6):1286-302. PubMed ID: 8651307
[TBL] [Abstract][Full Text] [Related]
32. Clinical, demographic, and genetic aspects of the Werner syndrome in Japan.
Goto M; Takeuchi F; Tanimoto K; Miyamoto T
Adv Exp Med Biol; 1985; 190():245-61. PubMed ID: 4083153
[TBL] [Abstract][Full Text] [Related]
33. Radiographic presentation of musculoskeletal involvement in Werner syndrome (adult progeria).
David A; Vincent M; Arrigoni PP; Barbarot S; Pistorius MA; Isidor B; Frampas E
Diagn Interv Imaging; 2017 May; 98(5):373-378. PubMed ID: 27931782
[TBL] [Abstract][Full Text] [Related]
34. Updated understanding of WRN variants using the Japanese whole-genome reference panel 3.5KJPNv2.
Fukunaga H; Prise KM; Taki Y
Geriatr Gerontol Int; 2019 Sep; 19(9):961-962. PubMed ID: 31490004
[No Abstract] [Full Text] [Related]
35. Leg ulcer in Werner syndrome (adult progeria): a case report.
Fumo G; Pau M; Patta F; Aste N; Atzori L
Dermatol Online J; 2013 Mar; 19(3):6. PubMed ID: 23552003
[TBL] [Abstract][Full Text] [Related]
36. Nakahara memorial lecture. Rare events and cancer epidemiology.
Miller RW
Princess Takamatsu Symp; 1987; 18():3-12. PubMed ID: 3333498
[TBL] [Abstract][Full Text] [Related]
37. Biallelic
Maezawa Y; Kato H; Takemoto M; Watanabe A; Koshizaka M; Ishikawa T; Sargolzaeiaval F; Kuzuya M; Wakabayashi H; Kusaka T; Yokote K; Oshima J
Mol Syndromol; 2018 Jul; 9(4):214-218. PubMed ID: 30140198
[TBL] [Abstract][Full Text] [Related]
38. Japanese diabetic patients with Werner syndrome exhibit high incidence of cancer.
Onishi S; Takemoto M; Ishikawa T; Okabe E; Ishibashi R; He P; Kobayashi K; Fujimoto M; Kawamura H; Yokote K
Acta Diabetol; 2012 Dec; 49 Suppl 1():S259-60. PubMed ID: 22872450
[No Abstract] [Full Text] [Related]
39. Primary liver tumor associated with Werner syndrome (adult progeria).
Okano H; Isono Y; Tanaka H; Ishihara Y; Matsusaki S; Aoki M; Sase T; Saitou T; Mukai K; Nishimura A; Takemoto M; Yokote K
Hepatol Res; 2011 Dec; 41(12):1260-5. PubMed ID: 22118305
[TBL] [Abstract][Full Text] [Related]
40. Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.
Nakura J; Miki T; Ye L; Mitsuda N; Zhao Y; Kihara K; Yu CE; Oshima J; Fukuchi KI; Wijsman EM; Schellenberg GD; Martin GM; Murano Si; Hashimoto K; Fujiwara Y; Ogihara T
Genomics; 1996 Aug; 36(1):130-41. PubMed ID: 8812424
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
