355 related articles for article (PubMed ID: 22541428)
1. Accumulation of the inner nuclear envelope protein Sun1 is pathogenic in progeric and dystrophic laminopathies.
Chen CY; Chi YH; Mutalif RA; Starost MF; Myers TG; Anderson SA; Stewart CL; Jeang KT
Cell; 2012 Apr; 149(3):565-77. PubMed ID: 22541428
[TBL] [Abstract][Full Text] [Related]
2. Reversal of laminopathies: the curious case of SUN1.
Chi YH; Chen CY; Jeang KT
Nucleus; 2012; 3(5):418-21. PubMed ID: 22895095
[TBL] [Abstract][Full Text] [Related]
3. Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes.
Haque F; Mazzeo D; Patel JT; Smallwood DT; Ellis JA; Shanahan CM; Shackleton S
J Biol Chem; 2010 Jan; 285(5):3487-98. PubMed ID: 19933576
[TBL] [Abstract][Full Text] [Related]
4. Dysregulated interactions between lamin A and SUN1 induce abnormalities in the nuclear envelope and endoplasmic reticulum in progeric laminopathies.
Chen ZJ; Wang WP; Chen YC; Wang JY; Lin WH; Tai LA; Liou GG; Yang CS; Chi YH
J Cell Sci; 2014 Apr; 127(Pt 8):1792-804. PubMed ID: 24522183
[TBL] [Abstract][Full Text] [Related]
5. LINC complex alterations in DMD and EDMD/CMT fibroblasts.
Taranum S; Vaylann E; Meinke P; Abraham S; Yang L; Neumann S; Karakesisoglou I; Wehnert M; Noegel AA
Eur J Cell Biol; 2012 Aug; 91(8):614-28. PubMed ID: 22555292
[TBL] [Abstract][Full Text] [Related]
6. Contribution of SUN1 mutations to the pathomechanism in muscular dystrophies.
Li P; Meinke P; Huong le TT; Wehnert M; Noegel AA
Hum Mutat; 2014 Apr; 35(4):452-61. PubMed ID: 24375709
[TBL] [Abstract][Full Text] [Related]
7. Lamin A/C Assembly Defects in
Bertrand AT; Brull A; Azibani F; Benarroch L; Chikhaoui K; Stewart CL; Medalia O; Ben Yaou R; Bonne G
Cells; 2020 Mar; 9(4):. PubMed ID: 32244403
[No Abstract] [Full Text] [Related]
8. Dysfunctional connections between the nucleus and the actin and microtubule networks in laminopathic models.
Hale CM; Shrestha AL; Khatau SB; Stewart-Hutchinson PJ; Hernandez L; Stewart CL; Hodzic D; Wirtz D
Biophys J; 2008 Dec; 95(11):5462-75. PubMed ID: 18790843
[TBL] [Abstract][Full Text] [Related]
9. Identification of mitochondrial dysfunction in Hutchinson-Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture.
Rivera-Torres J; Acín-Perez R; Cabezas-Sánchez P; Osorio FG; Gonzalez-Gómez C; Megias D; Cámara C; López-Otín C; Enríquez JA; Luque-García JL; Andrés V
J Proteomics; 2013 Oct; 91():466-77. PubMed ID: 23969228
[TBL] [Abstract][Full Text] [Related]
10. Everolimus rescues multiple cellular defects in laminopathy-patient fibroblasts.
DuBose AJ; Lichtenstein ST; Petrash NM; Erdos MR; Gordon LB; Collins FS
Proc Natl Acad Sci U S A; 2018 Apr; 115(16):4206-4211. PubMed ID: 29581305
[No Abstract] [Full Text] [Related]
11. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC
BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843
[TBL] [Abstract][Full Text] [Related]
12. Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle.
Mattioli E; Columbaro M; Capanni C; Maraldi NM; Cenni V; Scotlandi K; Marino MT; Merlini L; Squarzoni S; Lattanzi G
Cell Death Differ; 2011 Aug; 18(8):1305-15. PubMed ID: 21311568
[TBL] [Abstract][Full Text] [Related]
13. Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome.
Scaffidi P; Misteli T
Nat Med; 2005 Apr; 11(4):440-5. PubMed ID: 15750600
[TBL] [Abstract][Full Text] [Related]
14. The farnesyl transferase inhibitor (FTI) lonafarnib improves nuclear morphology in ZMPSTE24-deficient fibroblasts from patients with the progeroid disorder MAD-B.
Odinammadu KO; Shilagardi K; Tuminelli K; Judge DP; Gordon LB; Michaelis S
Nucleus; 2023 Dec; 14(1):2288476. PubMed ID: 38050983
[TBL] [Abstract][Full Text] [Related]
15. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
Bakay M; Wang Z; Melcon G; Schiltz L; Xuan J; Zhao P; Sartorelli V; Seo J; Pegoraro E; Angelini C; Shneiderman B; Escolar D; Chen YW; Winokur ST; Pachman LM; Fan C; Mandler R; Nevo Y; Gordon E; Zhu Y; Dong Y; Wang Y; Hoffman EP
Brain; 2006 Apr; 129(Pt 4):996-1013. PubMed ID: 16478798
[TBL] [Abstract][Full Text] [Related]
16. Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics.
Ho CY; Jaalouk DE; Vartiainen MK; Lammerding J
Nature; 2013 May; 497(7450):507-11. PubMed ID: 23644458
[TBL] [Abstract][Full Text] [Related]
17. FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy.
Ziat E; Mamchaoui K; Beuvin M; Nelson I; Azibani F; Spuler S; Bonne G; Bertrand AT
J Neuromuscul Dis; 2016 Nov; 3(4):497-510. PubMed ID: 27911330
[TBL] [Abstract][Full Text] [Related]
18. Emery-Dreifuss muscular dystrophy: focal point nuclear envelope.
Muchir A; Worman HJ
Curr Opin Neurol; 2019 Oct; 32(5):728-734. PubMed ID: 31460960
[TBL] [Abstract][Full Text] [Related]
19. Imbalanced nucleocytoskeletal connections create common polarity defects in progeria and physiological aging.
Chang W; Wang Y; Luxton GWG; Östlund C; Worman HJ; Gundersen GG
Proc Natl Acad Sci U S A; 2019 Feb; 116(9):3578-3583. PubMed ID: 30808750
[TBL] [Abstract][Full Text] [Related]
20. Inner nuclear envelope proteins SUN1 and SUN2 play a prominent role in the DNA damage response.
Lei K; Zhu X; Xu R; Shao C; Xu T; Zhuang Y; Han M
Curr Biol; 2012 Sep; 22(17):1609-15. PubMed ID: 22863315
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]