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Richard Gibbons
Richard Gibbons
Zweryfikowany adres z imm.ox.ac.uk
Tytuł
Cytowane przez
Cytowane przez
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Distinct factors control histone variant H3. 3 localization at specific genomic regions
AD Goldberg, LA Banaszynski, KM Noh, PW Lewis, SJ Elsaesser, ...
Cell 140 (5), 678-691, 2010
13592010
Prevalence and architecture of de novo mutations in developmental disorders
Nature 542 (7642), 433-438, 2017
8662017
Large-scale discovery of novel genetic causes of developmental disorders
Nature 519 (7542), 223-228, 2015
7362015
Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome)
RJ Gibbons, DJ Picketts, L Villard, DR Higgs
Cell 80 (6), 837-845, 1995
7171995
Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation
RJ Gibbons, TL McDowell, S Raman, DM O'Rourke, D Garrick, H Ayyub, ...
Nature genetics 24 (4), 368-371, 2000
5922000
Analysis of hundreds of cis-regulatory landscapes at high resolution in a single, high-throughput experiment
JR Hughes, N Roberts, S McGowan, D Hay, E Giannoulatou, M Lynch, ...
Nature genetics 46 (2), 205-212, 2014
5132014
ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner
MJ Law, KM Lower, HPJ Voon, JR Hughes, D Garrick, V Viprakasit, ...
Cell 143 (3), 367-378, 2010
4572010
The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies
Y Xue, R Gibbons, Z Yan, D Yang, TL McDowell, S Sechi, J Qin, S Zhou, ...
Proceedings of the National Academy of Sciences 100 (19), 10635-10640, 2003
4322003
Genetic dissection of the α-globin super-enhancer in vivo
D Hay, JR Hughes, C Babbs, JOJ Davies, BJ Graham, LLP Hanssen, ...
Nature genetics 48 (8), 895-903, 2016
3652016
A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter
M De Gobbi, V Viprakasit, JR Hughes, C Fisher, VJ Buckle, H Ayyub, ...
Science 312 (5777), 1215-1217, 2006
3592006
The Fanconi anemia pathway maintains genome stability by coordinating replication and transcription
RA Schwab, J Nieminuszczy, F Shah, J Langton, DL Martinez, CC Liang, ...
Molecular cell 60 (3), 351-361, 2015
3422015
Intragenic enhancers act as alternative promoters
MS Kowalczyk, JR Hughes, D Garrick, MD Lynch, JA Sharpe, ...
Molecular cell 45 (4), 447-458, 2012
3122012
ATRX Encodes a Novel Member of the SNF2 Family of Proteins: Mutations Point to a Common Mechanism Underlying the ATR-X Syndrome
DJ Picketts, DR Higgs, S Bachoo, DJ Blake, OWJ Quarrell, RJ Gibbons
Human molecular genetics 5 (12), 1899-1907, 1996
3031996
Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes
TL McDowell, RJ Gibbons, H Sutherland, DM O’Rourke, WA Bickmore, ...
Proceedings of the National Academy of Sciences 96 (24), 13983-13988, 1999
2961999
Suppression of the alternative lengthening of telomere pathway by the chromatin remodelling factor ATRX
D Clynes, C Jelinska, B Xella, H Ayyub, C Scott, M Mitson, S Taylor, ...
Nature communications 6 (1), 7538, 2015
2932015
Molecular–clinical spectrum of the ATR‐X syndrome
RJ Gibbons, DR Higgs
American journal of medical genetics 97 (3), 204-212, 2000
2502000
The norm of belief
J Gibbons
Oxford University Press, USA, 2013
2442013
The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis
NG Bérubé, M Mangelsdorf, M Jagla, J Vanderluit, D Garrick, RJ Gibbons, ...
The Journal of clinical investigation 115 (2), 258-267, 2005
2352005
An interspecies analysis reveals a key role for unmethylated CpG dinucleotides in vertebrate Polycomb complex recruitment
MD Lynch, AJH Smith, M De Gobbi, M Flenley, JR Hughes, D Vernimmen, ...
The EMBO journal 31 (2), 317-329, 2012
2322012
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain
RJ Gibbons, S Bachoo, DJ Picketts, S Aftimos, B Asenbauer, JA Bergoffen, ...
Nature genetics 17 (2), 146-148, 1997
2301997
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