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P. ARNAUD
P. ARNAUD
GReD CNRS & Université Clermont Auvergne
在 uca.fr 的电子邮件经过验证
标题
引用次数
引用次数
年份
Limited evolutionary conservation of imprinting in the human placenta
D Monk, P Arnaud, S Apostolidou, FA Hills, G Kelsey, P Stanier, R Feil, ...
Proceedings of the National Academy of Sciences 103 (17), 6623-6628, 2006
3022006
Erratum to: Deep sequencing and de novo assembly of the mouse occyte transcriptome define the contribution of transcription to the DNA methylation landscape
L Veselovska, SA Smallwood, H Saadeh, KR Stewart, F Krueger, ...
Genome biology 16 (1), 271, 2015
207*2015
Deep sequencing and de novo assembly of the mouse oocyte transcriptome define the contribution of transcription to the DNA methylation landscape
L Veselovska, SA Smallwood, H Saadeh, KR Stewart, F Krueger, ...
Genome biology 16 (1), 209, 2015
2072015
Deep sequencing and de novo assembly of the mouse oocyte transcriptome define the contribution of transcription to the DNA methylation landscape
L Veselovska, SA Smallwood, H Saadeh, KR Stewart, F Krueger, ...
Genome biology 16 (1), 209, 2015
2072015
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark
P Arnaud, D Monk, M Hitchins, E Gordon, W Dean, CV Beechey, J Peters, ...
Human molecular genetics 12 (9), 1005-1019, 2003
1802003
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human
D Monk, R Sanches, P Arnaud, S Apostolidou, FA Hills, S Abu-Amero, ...
Human molecular genetics 15 (8), 1259-1269, 2006
1702006
Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals
A Henckel, K Nakabayashi, LA Sanz, R Feil, K Hata, P Arnaud
Human molecular genetics 18 (18), 3375-3383, 2009
1642009
Epigenetic deregulation of genomic imprinting in human disorders and following assisted reproduction
P Arnaud, R Feil
Birth Defects Research Part C: Embryo Today: Reviews 75 (2), 81-97, 2005
1452005
Ring1B and Suv39h1 delineate distinct chromatin states at bivalent genes during early mouse lineage commitment
O Alder, F Lavial, A Helness, E Brookes, S Pinho, A Chandrashekran, ...
Development 137 (15), 2483-2492, 2010
1342010
Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus
C Coombes, P Arnaud, E Gordon, W Dean, EA Coar, CM Williamson, ...
Molecular and cellular biology 23 (16), 5475-5488, 2003
1332003
Genomic imprinting in germ cells: imprints are under control
P Arnaud
Reproduction 140 (3), 411-423, 2010
1312010
SINE retroposons can be used in vivo as nucleation centers for de novo methylation
P Arnaud, C Goubely, T Pélissier, JM Deragon
Molecular and cellular biology 20 (10), 3434-3441, 2000
1252000
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution
L Parker-Katiraee, AR Carson, T Yamada, P Arnaud, R Feil, ...
PLoS genetics 3 (5), e65, 2007
1092007
Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression
P Arnaud, D Monk, P Arnaud, J Frost, F Hills, P Stanier, R Feil, G Moore
105*2009
Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression
D Monk, P Arnaud, J Frost, FA Hills, P Stanier, R Feil, GE Moore
Human molecular genetics 18 (16), 3066-3074, 2009
1052009
Transcription and histone methylation changes correlate with imprint acquisition in male germ cells
A Henckel, K Chebli, SK Kota, P Arnaud, R Feil
The EMBO journal 31 (3), 606-615, 2012
952012
Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic …
D Monk, A Wagschal, P Arnaud, PS Müller, L Parker-Katiraee, D Bourc’his, ...
Genome research 18 (8), 1270-1281, 2008
952008
A mono‐allelic bivalent chromatin domain controls tissue‐specific imprinting at Grb10
LA Sanz, S Chamberlain, JC Sabourin, A Henckel, T Magnuson, ...
The EMBO journal 27 (19), 2523-2532, 2008
912008
Stochastic imprinting in the progeny of Dnmt3L−/− females
P Arnaud, K Hata, M Kaneda, E Li, H Sasaki, R Feil, G Kelsey
Human molecular genetics 15 (4), 589-598, 2006
822006
Genome-wide identification of new imprinted genes
A Henckel, P Arnaud
Briefings in functional genomics 9 (4), 304-314, 2010
762010
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