Blewitt ME, Blewitt M, Champ ME
Blewitt ME, Blewitt M, Champ ME
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Transgenerational inheritance of epigenetic states at the murine AxinFu allele occurs after maternal and paternal transmission
VK Rakyan, S Chong, ME Champ, PC Cuthbert, HD Morgan, KVK Luu, ...
Proceedings of the National Academy of Sciences 100 (5), 2538-2543, 2003
Metastable epialleles in mammals
VK Rakyan, ME Blewitt, R Druker, JI Preis, E Whitelaw
Trends in Genetics 18 (7), 348-351, 2002
Why weight? Modelling sample and observational level variability improves power in RNA-seq analyses
R Liu, AZ Holik, S Su, N Jansz, K Chen, HS Leong, ME Blewitt, ...
Nucleic acids research 43 (15), e97-e97, 2015
SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation
ME Blewitt, AV Gendrel, Z Pang, DB Sparrow, N Whitelaw, JM Craig, ...
Nature genetics 40 (5), 663-669, 2008
ChIP-seq analysis reveals distinct H3K27me3 profiles that correlate with transcriptional activity
MD Young, TA Willson, MJ Wakefield, E Trounson, DJ Hilton, ME Blewitt, ...
Nucleic acids research 39 (17), 7415-7427, 2011
Dynamic reprogramming of DNA methylation at an epigenetically sensitive allele in mice
ME Blewitt, NK Vickaryous, A Paldi, H Koseki, E Whitelaw
PLoS genetics 2 (4), e49, 2006
An N-ethyl-N-nitrosourea screen for genes involved in variegation in the mouse
ME Blewitt, NK Vickaryous, SJ Hemley, A Ashe, TJ Bruxner, JI Preis, ...
Proceedings of the National Academy of Sciences 102 (21), 7629-7634, 2005
Modifiers of epigenetic reprogramming show paternal effects in the mouse
S Chong, N Vickaryous, A Ashe, N Zamudio, N Youngson, S Hemley, ...
Nature genetics 39 (5), 614-622, 2007
Glimma: interactive graphics for gene expression analysis
S Su, CW Law, C Ah-Cann, ML Asselin-Labat, ME Blewitt, ME Ritchie
Bioinformatics 33 (13), 2050-2052, 2017
Opposing roles of polycomb repressive complexes in hematopoietic stem and progenitor cells
IJ Majewski, ME Ritchie, B Phipson, J Corbin, M Pakusch, A Ebert, ...
Blood, The Journal of the American Society of Hematology 116 (5), 731-739, 2010
Comprehensive characterization of distinct states of human naive pluripotency generated by reprogramming
X Liu, CM Nefzger, FJ Rossello, J Chen, AS Knaupp, J Firas, E Ford, ...
Nature methods 14 (11), 1055-1062, 2017
A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development
A Ashe, DK Morgan, NC Whitelaw, TJ Bruxner, NK Vickaryous, LL Cox, ...
Genome biology 9, 1-16, 2008
Genome-wide DNA methylation analysis identifies hypomethylated genes regulated by FOXP3 in human regulatory T cells
Y Zhang, J Maksimovic, G Naselli, J Qian, M Chopin, ME Blewitt, ...
Blood, The Journal of the American Society of Hematology 122 (16), 2823-2836, 2013
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
CT Gordon, S Xue, G Yigit, H Filali, K Chen, N Rosin, K Yoshiura, ...
Nature genetics 49 (2), 249-255, 2017
HBO1 is required for the maintenance of leukaemia stem cells
L MacPherson, J Anokye, MM Yeung, EYN Lam, YC Chan, CF Weng, ...
Nature 577 (7789), 266-270, 2020
Polycomb repressive complex 2 (PRC2) restricts hematopoietic stem cell activity
IJ Majewski, ME Blewitt, CA de Graaf, EJ McManus, M Bahlo, AA Hilton, ...
PLoS biology 6 (4), e93, 2008
edgeR: a versatile tool for the analysis of shRNA-seq and CRISPR-Cas9 genetic screens
Z Dai, JM Sheridan, LJ Gearing, DL Moore, S Su, S Wormald, S Wilcox, ...
F1000Research 3, 2014
MBD4 guards against methylation damage and germ line deficiency predisposes to clonal hematopoiesis and early-onset AML
MA Sanders, E Chew, C Flensburg, A Zeilemaker, SE Miller, AS Al Hinai, ...
Blood, The Journal of the American Society of Hematology 132 (14), 1526-1534, 2018
Genome-wide binding and mechanistic analyses of Smchd1-mediated epigenetic regulation
K Chen, J Hu, DL Moore, R Liu, SA Kessans, K Breslin, IS Lucet, A Keniry, ...
Proceedings of the National Academy of Sciences 112 (27), E3535-E3544, 2015
Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation
AW Mould, Z Pang, M Pakusch, ID Tonks, M Stark, D Carrie, ...
Epigenetics & chromatin 6, 1-16, 2013
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