These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 30057899)

  • 1. Lamin A, Chromatin and FPLD2: Not Just a Peripheral
    Briand N; Cahyani I; Madsen-Østerbye J; Paulsen J; Rønningen T; Sørensen AL; Collas P
    Front Cell Dev Biol; 2018; 6():73. PubMed ID: 30057899
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The lipodystrophic hotspot lamin A p.R482W mutation deregulates the mesodermal inducer T/Brachyury and early vascular differentiation gene networks.
    Briand N; Guénantin AC; Jeziorowska D; Shah A; Mantecon M; Capel E; Garcia M; Oldenburg A; Paulsen J; Hulot JS; Vigouroux C; Collas P
    Hum Mol Genet; 2018 Apr; 27(8):1447-1459. PubMed ID: 29438482
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Laminopathy-causing lamin A mutations reconfigure lamina-associated domains and local spatial chromatin conformation.
    Briand N; Collas P
    Nucleus; 2018 Jan; 9(1):216-226. PubMed ID: 29517398
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophy.
    Vadrot N; Duband-Goulet I; Cabet E; Attanda W; Barateau A; Vicart P; Gerbal F; Briand N; Vigouroux C; Oldenburg AR; Lund EG; Collas P; Buendia B
    Hum Mol Genet; 2015 Apr; 24(7):2096-109. PubMed ID: 25524705
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deregulation of Fragile X-related protein 1 by the lipodystrophic lamin A p.R482W mutation elicits a myogenic gene expression program in preadipocytes.
    Oldenburg AR; Delbarre E; Thiede B; Vigouroux C; Collas P
    Hum Mol Genet; 2014 Mar; 23(5):1151-62. PubMed ID: 24108105
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Depletion of lamins B1 and B2 promotes chromatin mobility and induces differential gene expression by a mesoscale-motion-dependent mechanism.
    Pujadas Liwag EM; Wei X; Acosta N; Carter LM; Yang J; Almassalha LM; Jain S; Daneshkhah A; Rao SSP; Seker-Polat F; MacQuarrie KL; Ibarra J; Agrawal V; Aiden EL; Kanemaki MT; Backman V; Adli M
    Genome Biol; 2024 Mar; 25(1):77. PubMed ID: 38519987
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lipodystrophy-linked LMNA p.R482W mutation induces clinical early atherosclerosis and in vitro endothelial dysfunction.
    Bidault G; Garcia M; Vantyghem MC; Ducluzeau PH; Morichon R; Thiyagarajah K; Moritz S; Capeau J; Vigouroux C; Béréziat V
    Arterioscler Thromb Vasc Biol; 2013 Sep; 33(9):2162-71. PubMed ID: 23846499
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular and Mechanobiological Pathways Related to the Physiopathology of FPLD2.
    Varlet AA; Helfer E; Badens C
    Cells; 2020 Aug; 9(9):. PubMed ID: 32842478
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Distinct features of lamin A-interacting chromatin domains mapped by ChIP-sequencing from sonicated or micrococcal nuclease-digested chromatin.
    Lund EG; Duband-Goulet I; Oldenburg A; Buendia B; Collas P
    Nucleus; 2015; 6(1):30-9. PubMed ID: 25602132
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A lipodystrophy-causing lamin A mutant alters conformation and epigenetic regulation of the anti-adipogenic
    Oldenburg A; Briand N; Sørensen AL; Cahyani I; Shah A; Moskaug JØ; Collas P
    J Cell Biol; 2017 Sep; 216(9):2731-2743. PubMed ID: 28751304
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lamin C is required to establish genome organization after mitosis.
    Wong X; Hoskins VE; Melendez-Perez AJ; Harr JC; Gordon M; Reddy KL
    Genome Biol; 2021 Nov; 22(1):305. PubMed ID: 34775987
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Role of lamins in 3D genome organization and global gene expression.
    Kim Y; Zheng X; Zheng Y
    Nucleus; 2019 Dec; 10(1):33-41. PubMed ID: 30755082
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization.
    Broers JL; Kuijpers HJ; Ostlund C; Worman HJ; Endert J; Ramaekers FC
    Exp Cell Res; 2005 Apr; 304(2):582-92. PubMed ID: 15748902
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of lamin A/C with muscle gene-specific promoters in myoblasts.
    Athar F; Parnaik VK
    Biochem Biophys Rep; 2015 Dec; 4():76-82. PubMed ID: 29124189
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy.
    Le Dour C; Wu W; Béréziat V; Capeau J; Vigouroux C; Worman HJ
    J Lipid Res; 2017 Jan; 58(1):151-163. PubMed ID: 27845687
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lamins Organize the Global Three-Dimensional Genome from the Nuclear Periphery.
    Zheng X; Hu J; Yue S; Kristiani L; Kim M; Sauria M; Taylor J; Kim Y; Zheng Y
    Mol Cell; 2018 Sep; 71(5):802-815.e7. PubMed ID: 30201095
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects.
    Håkelien AM; Delbarre E; Gaustad KG; Buendia B; Collas P
    Exp Cell Res; 2008 May; 314(8):1869-80. PubMed ID: 18396274
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lamin chromatin binding is modulated by interactions of different LAP2α domains with lamins and chromatin.
    Filipczak D; Souchet A; Georgiou K; Foisner R; Naetar N
    iScience; 2024 Oct; 27(10):110869. PubMed ID: 39319273
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lamina-associated domains: peripheral matters and internal affairs.
    Briand N; Collas P
    Genome Biol; 2020 Apr; 21(1):85. PubMed ID: 32241294
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A-type lamins bind both hetero- and euchromatin, the latter being regulated by lamina-associated polypeptide 2 alpha.
    Gesson K; Rescheneder P; Skoruppa MP; von Haeseler A; Dechat T; Foisner R
    Genome Res; 2016 Apr; 26(4):462-73. PubMed ID: 26798136
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.