Ikuti
Maria Eriksson
Maria Eriksson
Professor, Karolinska Institutet, Dept of Biosciences and Nutrition
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Dikutip oleh
Dikutip oleh
Tahun
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
M Eriksson, WT Brown, LB Gordon, MW Glynn, J Singer, L Scott, ...
Nature 423 (6937), 293-298, 2003
25822003
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome
RD Goldman, DK Shumaker, MR Erdos, M Eriksson, AE Goldman, ...
Proceedings of the National Academy of Sciences 101 (24), 8963-8968, 2004
13032004
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging
DK Shumaker, T Dechat, A Kohlmaier, SA Adam, MR Bozovsky, ...
Proceedings of the National Academy of Sciences 103 (23), 8703-8708, 2006
8872006
Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson–Gilford progeria syndrome
R Varga, M Eriksson, MR Erdos, M Olive, I Harten, F Kolodgie, BC Capell, ...
Proceedings of the National Academy of Sciences 103 (9), 3250-3255, 2006
3182006
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging
S Rodriguez, F Coppede, H Sagelius, M Eriksson
European journal of human genetics 17 (7), 928-937, 2009
1562009
Somatic mutagenesis in satellite cells associates with human skeletal muscle aging
I Franco, A Johansson, K Olsson, P Vrtačnik, P Lundin, HT Helgadottir, ...
Nature communications 9 (1), 800, 2018
1362018
Inhibition of DNA damage response at telomeres improves the detrimental phenotypes of Hutchinson–Gilford Progeria Syndrome
J Aguado, A Sola-Carvajal, V Cancila, G Revêchon, PF Ong, ...
Nature communications 10 (1), 4990, 2019
1192019
Endothelial progerin expression causes cardiovascular pathology through an impaired mechanoresponse
S Osmanagic-Myers, A Kiss, C Manakanatas, O Hamza, F Sedlmayer, ...
The Journal of clinical investigation 129 (2), 531-545, 2019
1152019
Stem cell depletion in Hutchinson–Gilford progeria syndrome
Y Rosengardten, T McKenna, D Grochová, M Eriksson
Aging cell 10 (6), 1011-1020, 2011
1112011
The role of epigenetics in renal ageing
PG Shiels, D McGuinness, M Eriksson, JP Kooman, P Stenvinkel
Nature Reviews Nephrology 13 (8), 471-482, 2017
1082017
Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
H Sagelius, Y Rosengardten, M Hanif, MR Erdos, B Rozell, FS Collins, ...
Journal of cell science 121 (7), 969-978, 2008
992008
Global genome splicing analysis reveals an increased number of alternatively spliced genes with aging
SA Rodríguez, D Grochová, T McKenna, B Borate, NS Trivedi, MR Erdos, ...
Aging cell 15 (2), 267-278, 2016
972016
Founder Mutation in RSPH4A Identified in Patients of Hispanic Descent with Primary Ciliary Dyskinesia
MLA Daniels, MW Leigh, SD Davis, MC Armstrong, JL Carson, ...
Human mutation 34 (10), 1352-1356, 2013
782013
Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type
I Franco, HT Helgadottir, A Moggio, M Larsson, P Vrtačnik, A Johansson, ...
Genome biology 20 (1), 1-22, 2019
662019
Reversible phenotype in a mouse model of Hutchinson–Gilford progeria syndrome
H Sagelius, Y Rosengardten, E Schmidt, C Sonnabend, B Rozell, ...
Journal of medical genetics 45 (12), 794-801, 2008
592008
Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 …
M Eriksson, T Ansved, L Edström, M Anvret, N Carey
Human molecular genetics 8 (6), 1053-1060, 1999
541999
Expression of the Hutchinson-Gilford progeria mutation during osteoblast development results in loss of osteocytes, irregular mineralization, and poor biomechanical properties
E Schmidt, O Nilsson, A Koskela, J Tuukkanen, C Ohlsson, B Rozell, ...
Journal of biological chemistry 287 (40), 33512-33522, 2012
532012
Embryonic expression of the common progeroid lamin A splice mutation arrests postnatal skin development
T McKenna, Y Rosengardten, N Viceconte, JH Baek, D Grochova, ...
Aging cell 13 (2), 292-302, 2014
492014
Failure to achieve gene conversion with chimeric circular oligonucleotides: potentially misleading PCR artifacts observed
Z ZHANG, M ERIKSSON, G FALK, C GRAFF, SC PRESNELL, MS READ, ...
Antisense and Nucleic Acid Drug Development 8 (6), 531-536, 1998
481998
Characterization of lamin Mutation Phenotypes in Drosophila and Comparison to Human Laminopathies
A Muñoz-Alarcón, M Pavlovic, J Wismar, B Schmitt, M Eriksson, P Kylsten, ...
PloS one 2 (6), e532, 2007
422007
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