Format
Sort by

Send to

Choose Destination

Search results

Items: 4

1.

Expression of the Hutchinson-Gilford Progeria Mutation Leads to Aberrant Dentin Formation.

Choi H, Kim TH, Jeong JK, Strandgren C, Eriksson M, Cho ES.

Sci Rep. 2018 Oct 18;8(1):15368. doi: 10.1038/s41598-018-33764-6.

2.

Emerging candidate treatment strategies for Hutchinson-Gilford progeria syndrome.

Strandgren C, RevĂȘchon G, Sola-Carvajal A, Eriksson M.

Biochem Soc Trans. 2017 Dec 15;45(6):1279-1293. doi: 10.1042/BST20170141. Epub 2017 Nov 10. Review.

PMID:
29127216
3.

Transgene silencing of the Hutchinson-Gilford progeria syndrome mutation results in a reversible bone phenotype, whereas resveratrol treatment does not show overall beneficial effects.

Strandgren C, Nasser HA, McKenna T, Koskela A, Tuukkanen J, Ohlsson C, Rozell B, Eriksson M.

FASEB J. 2015 Aug;29(8):3193-205. doi: 10.1096/fj.14-269217. Epub 2015 Apr 15.

4.

Expression of progerin in aging mouse brains reveals structural nuclear abnormalities without detectible significant alterations in gene expression, hippocampal stem cells or behavior.

Baek JH, Schmidt E, Viceconte N, Strandgren C, Pernold K, Richard TJ, Van Leeuwen FW, Dantuma NP, Damberg P, Hultenby K, Ulfhake B, Mugnaini E, Rozell B, Eriksson M.

Hum Mol Genet. 2015 Mar 1;24(5):1305-21. doi: 10.1093/hmg/ddu541. Epub 2014 Oct 24.

Supplemental Content

Loading ...
Support Center