306 related articles for article (PubMed ID: 23257959)
1. Aberrant DNA methylation profiles in the premature aging disorders Hutchinson-Gilford Progeria and Werner syndrome.
Heyn H; Moran S; Esteller M
Epigenetics; 2013 Jan; 8(1):28-33. PubMed ID: 23257959
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome.
Wu Z; Zhang W; Song M; Wang W; Wei G; Li W; Lei J; Huang Y; Sang Y; Chan P; Chen C; Qu J; Suzuki K; Belmonte JCI; Liu GH
Protein Cell; 2018 Apr; 9(4):333-350. PubMed ID: 29476423
[TBL] [Abstract][Full Text] [Related]
4. Understanding Vascular Diseases: Lessons From Premature Aging Syndromes.
Ikeda Y; Kumagai H; Motozawa Y; Suzuki J; Akazawa H; Komuro I
Can J Cardiol; 2016 May; 32(5):650-8. PubMed ID: 26948039
[TBL] [Abstract][Full Text] [Related]
5. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes.
Maierhofer A; Flunkert J; Oshima J; Martin GM; Poot M; Nanda I; Dittrich M; Müller T; Haaf T
Aging Cell; 2019 Oct; 18(5):e12995. PubMed ID: 31259468
[TBL] [Abstract][Full Text] [Related]
6. DNA methylation signatures in Blood DNA of Hutchinson-Gilford Progeria syndrome.
Bejaoui Y; Razzaq A; Yousri NA; Oshima J; Megarbane A; Qannan A; Potabattula R; Alam T; Martin GM; Horn HF; Haaf T; Horvath S; El Hajj N
Aging Cell; 2022 Feb; 21(2):e13555. PubMed ID: 35045206
[TBL] [Abstract][Full Text] [Related]
7. Prematurely aged children: molecular alterations leading to Hutchinson-Gilford progeria and Werner syndromes.
Domínguez-Gerpe L; Araújo-Vilar D
Curr Aging Sci; 2008 Dec; 1(3):202-12. PubMed ID: 20021393
[TBL] [Abstract][Full Text] [Related]
8. Mechanisms of cardiovascular disease in accelerated aging syndromes.
Capell BC; Collins FS; Nabel EG
Circ Res; 2007 Jul; 101(1):13-26. PubMed ID: 17615378
[TBL] [Abstract][Full Text] [Related]
9. [Molecular mechanism of pathogenesis of the progeria].
Shimizu T; Yokote K
Nihon Rinsho; 2016 Sep; 74(9):1572-1576. PubMed ID: 30557495
[TBL] [Abstract][Full Text] [Related]
10. LMNA mutations in progeroid syndromes.
Huang S; Kennedy BK; Oshima J
Novartis Found Symp; 2005; 264():197-202; discussion 202-7, 227-30. PubMed ID: 15773755
[TBL] [Abstract][Full Text] [Related]
11. Epigenetic deregulation of lamina-associated domains in Hutchinson-Gilford progeria syndrome.
Köhler F; Bormann F; Raddatz G; Gutekunst J; Corless S; Musch T; Lonsdorf AS; Erhardt S; Lyko F; Rodríguez-Paredes M
Genome Med; 2020 May; 12(1):46. PubMed ID: 32450911
[TBL] [Abstract][Full Text] [Related]
12. Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A.
Kang SM; Yoon MH; Lee SJ; Ahn J; Yi SA; Nam KH; Park S; Woo TG; Cho JH; Lee J; Ha NC; Park BJ
Sci Rep; 2021 Apr; 11(1):9122. PubMed ID: 33907225
[TBL] [Abstract][Full Text] [Related]
13. Premature aging syndrome.
Coppedè F
Adv Exp Med Biol; 2012; 724():317-31. PubMed ID: 22411253
[TBL] [Abstract][Full Text] [Related]
14. Accelerated epigenetic aging in Werner syndrome.
Maierhofer A; Flunkert J; Oshima J; Martin GM; Haaf T; Horvath S
Aging (Albany NY); 2017 Apr; 9(4):1143-1152. PubMed ID: 28377537
[TBL] [Abstract][Full Text] [Related]
15. Werner and Hutchinson-Gilford progeria syndromes: mechanistic basis of human progeroid diseases.
Kudlow BA; Kennedy BK; Monnat RJ
Nat Rev Mol Cell Biol; 2007 May; 8(5):394-404. PubMed ID: 17450177
[TBL] [Abstract][Full Text] [Related]
16. Model of human aging: recent findings on Werner's and Hutchinson-Gilford progeria syndromes.
Ding SL; Shen CY
Clin Interv Aging; 2008; 3(3):431-44. PubMed ID: 18982914
[TBL] [Abstract][Full Text] [Related]
17. Atherosclerosis and Cardiovascular Diseases in Progeroid Syndromes.
Kato H; Maezawa Y
J Atheroscler Thromb; 2022 Apr; 29(4):439-447. PubMed ID: 34511576
[TBL] [Abstract][Full Text] [Related]
18. Accelerated aging syndromes, are they relevant to normal human aging?
Dreesen O; Stewart CL
Aging (Albany NY); 2011 Sep; 3(9):889-95. PubMed ID: 21931180
[TBL] [Abstract][Full Text] [Related]
19. Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations.
Gonzalo S; Kreienkamp R; Askjaer P
Ageing Res Rev; 2017 Jan; 33():18-29. PubMed ID: 27374873
[TBL] [Abstract][Full Text] [Related]
20. Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.
Hisama FM; Lessel D; Leistritz D; Friedrich K; McBride KL; Pastore MT; Gottesman GS; Saha B; Martin GM; Kubisch C; Oshima J
Am J Med Genet A; 2011 Dec; 155A(12):3002-6. PubMed ID: 22065502
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
