294 related articles for article (PubMed ID: 31647095)
1. Lamin A/C promotes DNA base excision repair.
Maynard S; Keijzers G; Akbari M; Ezra MB; Hall A; Morevati M; Scheibye-Knudsen M; Gonzalo S; Bartek J; Bohr VA
Nucleic Acids Res; 2019 Dec; 47(22):11709-11728. PubMed ID: 31647095
[TBL] [Abstract][Full Text] [Related]
2. Towards delineating the chain of events that cause premature senescence in the accelerated aging syndrome Hutchinson-Gilford progeria (HGPS).
Dreesen O
Biochem Soc Trans; 2020 Jun; 48(3):981-991. PubMed ID: 32539085
[TBL] [Abstract][Full Text] [Related]
3. Vitamin D receptor signaling improves Hutchinson-Gilford progeria syndrome cellular phenotypes.
Kreienkamp R; Croke M; Neumann MA; Bedia-Diaz G; Graziano S; Dusso A; Dorsett D; Carlberg C; Gonzalo S
Oncotarget; 2016 May; 7(21):30018-31. PubMed ID: 27145372
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Altered modulation of lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS.
Mattioli E; Andrenacci D; Garofalo C; Prencipe S; Scotlandi K; Remondini D; Gentilini D; Di Blasio AM; Valente S; Scarano E; Cicchilitti L; Piaggio G; Mai A; Lattanzi G
Aging Cell; 2018 Oct; 17(5):e12824. PubMed ID: 30109767
[TBL] [Abstract][Full Text] [Related]
6. Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.
Cau P; Navarro C; Harhouri K; Roll P; Sigaudy S; Kaspi E; Perrin S; De Sandre-Giovannoli A; Lévy N
Semin Cell Dev Biol; 2014 May; 29():125-47. PubMed ID: 24662892
[TBL] [Abstract][Full Text] [Related]
7. [The role of lamins and mutations of LMNA gene in physiological and premature aging].
Sliwińska MA
Postepy Biochem; 2007; 53(1):46-52. PubMed ID: 17718387
[TBL] [Abstract][Full Text] [Related]
8. Gene expression profiling of fibroblasts in a family with LMNA-related cardiomyopathy reveals molecular pathways implicated in disease pathogenesis.
Widyastuti HP; Norden-Krichmar TM; Grosberg A; Zaragoza MV
BMC Med Genet; 2020 Jul; 21(1):152. PubMed ID: 32698886
[TBL] [Abstract][Full Text] [Related]
9. Premature aging syndromes: From patients to mechanism.
Foo MXR; Ong PF; Dreesen O
J Dermatol Sci; 2019 Nov; 96(2):58-65. PubMed ID: 31727429
[TBL] [Abstract][Full Text] [Related]
10. Hutchinson-Gilford progeria syndrome through the lens of transcription.
Prokocimer M; Barkan R; Gruenbaum Y
Aging Cell; 2013 Aug; 12(4):533-43. PubMed ID: 23496208
[TBL] [Abstract][Full Text] [Related]
11. Sustained accumulation of prelamin A and depletion of lamin A/C both cause oxidative stress and mitochondrial dysfunction but induce different cell fates.
Sieprath T; Corne TD; Nooteboom M; Grootaert C; Rajkovic A; Buysschaert B; Robijns J; Broers JL; Ramaekers FC; Koopman WJ; Willems PH; De Vos WH
Nucleus; 2015; 6(3):236-46. PubMed ID: 25996284
[TBL] [Abstract][Full Text] [Related]
12. Distinct structural and mechanical properties of the nuclear lamina in Hutchinson-Gilford progeria syndrome.
Dahl KN; Scaffidi P; Islam MF; Yodh AG; Wilson KL; Misteli T
Proc Natl Acad Sci U S A; 2006 Jul; 103(27):10271-10276. PubMed ID: 16801550
[TBL] [Abstract][Full Text] [Related]
13. Lamin A Is an Endogenous SIRT6 Activator and Promotes SIRT6-Mediated DNA Repair.
Ghosh S; Liu B; Wang Y; Hao Q; Zhou Z
Cell Rep; 2015 Nov; 13(7):1396-1406. PubMed ID: 26549451
[TBL] [Abstract][Full Text] [Related]
14. Hutchinson-Gilford Progeria Syndrome: An Overview of the Molecular Mechanism, Pathophysiology and Therapeutic Approach.
Rahman MM; Ferdous KS; Ahmed M; Islam MT; Khan MR; Perveen A; Ashraf GM; Uddin MS
Curr Gene Ther; 2021; 21(3):216-229. PubMed ID: 33655857
[TBL] [Abstract][Full Text] [Related]
15. Lamin A/C impairments cause mitochondrial dysfunction by attenuating PGC1α and the NAMPT-NAD+ pathway.
Maynard S; Hall A; Galanos P; Rizza S; Yamamoto T; Gram HH; Munk SHN; Shoaib M; Sørensen CS; Bohr VA; Lerdrup M; Maya-Mendoza A; Bartek J
Nucleic Acids Res; 2022 Sep; 50(17):9948-9965. PubMed ID: 36099415
[TBL] [Abstract][Full Text] [Related]
16. Hutchinson-Gilford progeria syndrome.
Pollex RL; Hegele RA
Clin Genet; 2004 Nov; 66(5):375-81. PubMed ID: 15479179
[TBL] [Abstract][Full Text] [Related]
17. Nuclear lamin phosphorylation: an emerging role in gene regulation and pathogenesis of laminopathies.
Liu SY; Ikegami K
Nucleus; 2020 Dec; 11(1):299-314. PubMed ID: 33030403
[TBL] [Abstract][Full Text] [Related]
18. LMNA Mutation c.917T>G (p.L306R) Leads to Deleterious Hyper-Assembly of Lamin A/C and Associates with Severe Right Ventricular Cardiomyopathy and Premature Aging.
Alastalo TP; West G; Li SP; Keinänen A; Helenius M; Tyni T; Lapatto R; Turanlahti M; Heikkilä P; Kääriäinen H; Laakso M; Mauermann M; Herrmann H; Pihkala J; Taimen P
Hum Mutat; 2015 Jul; 36(7):694-703. PubMed ID: 25820511
[TBL] [Abstract][Full Text] [Related]
19. Lamin A Δexon9 mutation leads to telomere and chromatin defects but not genomic instability.
Das A; Grotsky DA; Neumann MA; Kreienkamp R; Gonzalez-Suarez I; Redwood AB; Kennedy BK; Stewart CL; Gonzalo S
Nucleus; 2013; 4(5):410-9. PubMed ID: 24153156
[TBL] [Abstract][Full Text] [Related]
20. DNA repair defects and genome instability in Hutchinson-Gilford Progeria Syndrome.
Gonzalo S; Kreienkamp R
Curr Opin Cell Biol; 2015 Jun; 34():75-83. PubMed ID: 26079711
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
