234 related articles for article (PubMed ID: 23324461)
1. Soft substrates normalize nuclear morphology and prevent nuclear rupture in fibroblasts from a laminopathy patient with compound heterozygous LMNA mutations.
Tamiello C; Kamps MA; van den Wijngaard A; Verstraeten VL; Baaijens FP; Broers JL; Bouten CC
Nucleus; 2013; 4(1):61-73. PubMed ID: 23324461
[TBL] [Abstract][Full Text] [Related]
2. Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.
Broers JL; Peeters EA; Kuijpers HJ; Endert J; Bouten CV; Oomens CW; Baaijens FP; Ramaekers FC
Hum Mol Genet; 2004 Nov; 13(21):2567-80. PubMed ID: 15367494
[TBL] [Abstract][Full Text] [Related]
3. Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations.
Core JQ; Mehrabi M; Robinson ZR; Ochs AR; McCarthy LA; Zaragoza MV; Grosberg A
PLoS One; 2017; 12(11):e0188256. PubMed ID: 29149195
[TBL] [Abstract][Full Text] [Related]
4. A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus.
Barateau A; Vadrot N; Vicart P; Ferreiro A; Mayer M; Héron D; Vigouroux C; Buendia B
PLoS One; 2017; 12(1):e0169189. PubMed ID: 28125586
[TBL] [Abstract][Full Text] [Related]
5. Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress.
Paradisi M; McClintock D; Boguslavsky RL; Pedicelli C; Worman HJ; Djabali K
BMC Cell Biol; 2005 Jun; 6():27. PubMed ID: 15982412
[TBL] [Abstract][Full Text] [Related]
6. Increased plasticity of the nuclear envelope and hypermobility of telomeres due to the loss of A-type lamins.
De Vos WH; Houben F; Hoebe RA; Hennekam R; van Engelen B; Manders EM; Ramaekers FC; Broers JL; Van Oostveldt P
Biochim Biophys Acta; 2010 Apr; 1800(4):448-58. PubMed ID: 20079404
[TBL] [Abstract][Full Text] [Related]
7. Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria.
Ikegami K; Secchia S; Almakki O; Lieb JD; Moskowitz IP
Dev Cell; 2020 Mar; 52(6):699-713.e11. PubMed ID: 32208162
[TBL] [Abstract][Full Text] [Related]
8. Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy.
Forleo C; Carmosino M; Resta N; Rampazzo A; Valecce R; Sorrentino S; Iacoviello M; Pisani F; Procino G; Gerbino A; Scardapane A; Simone C; Calore M; Torretta S; Svelto M; Favale S
PLoS One; 2015; 10(4):e0121723. PubMed ID: 25837155
[TBL] [Abstract][Full Text] [Related]
9. Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition.
Glynn MW; Glover TW
Hum Mol Genet; 2005 Oct; 14(20):2959-69. PubMed ID: 16126733
[TBL] [Abstract][Full Text] [Related]
10. Nuclear Abnormalities in
Wilke MVMB; Wick M; Schwab TL; Starosta RT; Clark KJ; Connolly HM; Klee EW
Genes (Basel); 2024 Jan; 15(1):. PubMed ID: 38255001
[TBL] [Abstract][Full Text] [Related]
11. Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells.
Kandert S; Lüke Y; Kleinhenz T; Neumann S; Lu W; Jaeger VM; Munck M; Wehnert M; Müller CR; Zhou Z; Noegel AA; Dabauvalle MC; Karakesisoglou I
Hum Mol Genet; 2007 Dec; 16(23):2944-59. PubMed ID: 17881656
[TBL] [Abstract][Full Text] [Related]
12. Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling.
Zwerger M; Jaalouk DE; Lombardi ML; Isermann P; Mauermann M; Dialynas G; Herrmann H; Wallrath LL; Lammerding J
Hum Mol Genet; 2013 Jun; 22(12):2335-49. PubMed ID: 23427149
[TBL] [Abstract][Full Text] [Related]
13. Current insights into LMNA cardiomyopathies: Existing models and missing LINCs.
Brayson D; Shanahan CM
Nucleus; 2017 Jan; 8(1):17-33. PubMed ID: 28125396
[TBL] [Abstract][Full Text] [Related]
14. Mechanics in human fibroblasts and progeria: Lamin A mutation E145K results in stiffening of nuclei.
Apte K; Stick R; Radmacher M
J Mol Recognit; 2017 Feb; 30(2):. PubMed ID: 27677907
[TBL] [Abstract][Full Text] [Related]
15. Collagen expression in fibroblasts with a novel LMNA mutation.
Nguyen D; Leistritz DF; Turner L; MacGregor D; Ohson K; Dancey P; Martin GM; Oshima J
Biochem Biophys Res Commun; 2007 Jan; 352(3):603-8. PubMed ID: 17150192
[TBL] [Abstract][Full Text] [Related]
16. LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).
Cao H; Hegele RA
J Hum Genet; 2003; 48(5):271-274. PubMed ID: 12768443
[TBL] [Abstract][Full Text] [Related]
17. Protein structural and mechanistic basis of progeroid laminopathies.
Marcelot A; Worman HJ; Zinn-Justin S
FEBS J; 2021 May; 288(9):2757-2772. PubMed ID: 32799420
[TBL] [Abstract][Full Text] [Related]
18. Eliminating the synthesis of mature lamin A reduces disease phenotypes in mice carrying a Hutchinson-Gilford progeria syndrome allele.
Yang SH; Qiao X; Farber E; Chang SY; Fong LG; Young SG
J Biol Chem; 2008 Mar; 283(11):7094-9. PubMed ID: 18178963
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genotype-phenotype analysis of LMNA-related diseases predicts phenotype-selective alterations in lamin phosphorylation.
Lin EW; Brady GF; Kwan R; Nesvizhskii AI; Omary MB
FASEB J; 2020 Jul; 34(7):9051-9073. PubMed ID: 32413188
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
