Zobrazeno 1 - 10
of 230
pro vyhledávání: '"E. Viegas-Péquignot"'
Autor:
Déborah Bourc'his, M. Jeanpierre, L. Tiepolo, E. Viegas-Péquignot, P. Maraschio, Pierre Miniou, D. Molina Gomes, Jean-Michel Dupont, G. De Saint-Basile
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
DNA undermethylation is a characteristic feature of ICF syndrome and has been implicated in the formation of the juxtacentromeric chromosomal abnormalities of this rare syndrome. We have previously shown that in female ICF patients the inactive X chr
Autor:
Tina Rich, Muriel Rigolet, E. Viegas-Péquignot, Claudine Junien, Denise Molina-Gomes, Marie-Sylvie Gross-Morand
Publikováno v:
DNA Research. 5:309-313
A cDNA e encoding the human Id4 protein has been isolated from an astrocytoma library. The predicted protein product shares 98% identity with the mouse Id4 protein and is markedly different from that already reported. By FISH analysis, the human ID4
Autor:
A. Niveleau, L.F. de Almeida-Toledo, E. Viegas-Péquignot, Fausto Foresti, S. de Almeida Toledo-Filho, A.C. Coutinho-Barbosa
Publikováno v:
Cytogenetic and Genome Research. 83:21-24
The distribution of 5-methylcytosine (5-MeC) was investigated in fish chromosomes by indirect immunofluorescence using a highly specific 5-MeC monoclonal antibody. Diploid and artificially produced triploid specimens of the pacu fish, Piaractus mesop
Autor:
S. Sakon, M. Hori, Tom Goldammer, P. Stanier, H. Nishimori, S. Châtelin, L.D. Coogle, J. Kaplan, W.J. Kimberling, H.C. Ardley, A.J. Brookes, H. Hirota, C. Janish, J. Eddleston, R. Matsuoka, Manfred Schwerin, M.Z. Limongi, K. Akagawa, A. Vilain, M. Schmid, M.H. Adams, M. Tamari, T. Kawabe, T. Katagiri, D. Diamond, X. Wang, D. Sundaramurthy, S. Ishikawa, M. Mihara, J. Surrallés, S. Sonta, G. Meroni, P.A. Robinson, G. Del Sal, K.S. Reddy, A. Munnich, F.C. Kischkel, O.T. Tap, G. Della Valle, L.F. Pieri, J. Neesen, Y. Daigo, E. Viegas-Péquignot, F.S. Grass, E. Crawford, K. Weipoltshammer, I. Perrault, R.P. Kimberly, G.R. Rutteman, K.J. McDowell, F. Wachtler, Y. Nakamura, K.S. Theil, T. Ono, K. Gardiner, K.J. Fowler, T. Tetsuka, T. Emahazion, R.G. Brzyski, J. McKeand, B. Malfoy, A.J. Copp, C.M. Moore, D. Molina-Gomez, P. Calvas, R.G. Best, P. Franz, A. Ueno, D.M. Hoover, M. Yokoyama, H. Otsuka, L. Gaddini, T. Nakada, M. Tham, M. Gostissa, O. Maruyama, J. Vanselow, A. Beskow, D.A. Campbell, M.R. Koehler, N. Shimizu, K.H.A. Choo, K. Mikoshiba, J.B. Kenyon, K. Kirschhofer, J.N. Murdoch, A.A. Bosma, H. Satoh, S. Weitz, S. Abu-Hayyeh, J.-M. Rozet, H. Yagita, C. Sreekantaiah, A. Poustka, C. Zijlstra, C.L. Anderson, N.A. de Haan, M.-L. Yaspo, P. Sandy, V. Sulcova, U. Gyllensten, N.D. Sullivan, T. Toki, A.A. Szalay, J. Rogers, Y. Miki, K. Chida, L.L. Culley, D.F. Hudson, T.L. Lear, D. Soenksen, J.-P. Yang, F. Pelliccia, M. Yamamoto, M.M. Bouzyk, X. Li, F. Apiou, K. Kogame, D.V. Irvine, M.M. Leland, T. Kuroki, R. Saffery, A. Rocchi, D.L. Maresco, B. Dutrillaux, H. Nakano, A.T. Natarajan, R. Fürbass, P. Lichter, K. Okumura, E. Souied, E. Ito, J.P. Leek, M. Kimura, A.F. Markham, Ronald M. Brunner, P. Kioschis, P.H. Krammer, S. Saccone, S. Gerber, T. Iwata, B.T. Kile, H.E. Trowell, Y. Shimizu, M. Shindo, T. Nakayama, T. Okamoto, E. Bailey, L.E. Blue, S.M. Witte
Publikováno v:
Cytogenetic and Genome Research. 82:131-144
Autor:
Marc Jeanpierre, Déborah Bourc'his, Pierre Miniou, E. Viegas-Péquignot, Véronique Blanquet, Ana Carolina Coutinho Barbosa
Publikováno v:
Human Genetics. 99:738-745
The methylation profile of ten alpha-satellites was investigated in normal individuals and in ICF (Immunodeficiency, Centromeric instability, Facial abnormalities) patients. Two out of three ICF patients showed modified methylation of these sequences
Autor:
A. Botta, K. Rojas, P. Zaragoza, X.-X. Zhang, M. Pritchard, B.P. Chowdhary, J.P. Park, J.L. Kissil, A. Rocchi, T.K. Watanabe, T. Siddque, N.P. Mertvetsov, W. Engel, A.A. Bosma, C. Rodellar, A. Arai, F. Shimizu, B. Hoebee, K.N. Sastry, R. Houlgatte, P.A. Voûte, N. Guo, U.W. Kenkare, J.-J. Cassiman, J. Guimera, W.R. Harrison, M.Z. Limongi, G. Mirza, A. Fratello, C.H. van Os, T. Ikeuchi, M. Chaffanet, T. Goldammer, M. Mannens, D. Grady, D. Wells, V. Romano, O. Miura, As. Ricco, M. Schwerin, M. Gersh, M.L. Filipenko, S.A. Wilcox, H. Levéziel, S.J. O’Brien, G.F.M. Merkx, C.C. Morton, G. Hardiman, R. Marzella, S. Hirosawa, T.J. Robinson, K.B.M. Reid, C. Elduque, A.S. Hewson, P.M.T. Deen, J.A. Squire, J.A.M. Graves, L. Vatteroni, E. Viegas-Péquignot, K. Yamamoto, M. Carter, L. Frönicke, N.V. Vorobieva, J. Overhauser, N. Ceratto, N.A. de Haan, M. Suzuki, T. Kozaki, M.S. Aly, B. Redeker, S. van Beersum, P.M. Borodin, F.F.B. Elder, A. Kimchi, A.S. Graphodatsky, B. Beatty, J.A. McMahon, M. de Meulemeester, J.B. Searle, I.V. Koroleva, W.Y. Hung, Y. Kuga, M. Jeanpierre, N. Sakuragawa, S. Feo, C. Auffray, M. Ogawa, M. Rocchi, M.P. Hande, C.K. Ullrich, J. Widmer, A. Ponce de León, F.O. Fackelmayer, S. Weremowicz, A. Pizzuti, K. Ohsugi, S. Okuno, R.J.M. Bindels, L.D. Matyakhina, A.P. McMahon, R. Leube, Y. Yang, A. Pandita, M. Lachtermacher, A. Tanzariello, B. Dallapiccola, M.A. Ferguson-Smith, A. Musio, A.F. Davies, D. Patterson, N. Lynch, Y. Nakamura, G. Rainaldi, M. Steenman, S.-T. Lee, H. Hayes, P.C.M. O’Brien, G.G. Karpova, C.H.M. Mellink, E. Jenkins, J.H. Xia, M. Schepens, A.T. Natarajan, B.-L. Lim, R. Meneveri, W.G. Nash, J. Kissing, M. Stacey, T. Fujiwara, M. Schmid, L.A. Witters, C. Zijlstra, L. Viggiano, F. Yang, M. Nagata, W. Bie, H. Scherthan, H. Murer, B. Ghebrehiwet, A. Westerveld, S. Kurata, H.N. Seuánez, M. Lovett, K.-H. Lee, R. Godbout, H.G. Brunner, J.M. Varley, P. Thygesen, R. Slater, S. Ishikawa, S.D. Pack, E. Takahashi, O.V. Cheryaukene, C. Bendixen, F. Ugolini, M. Matsumoto, R.M. Brunner, A. Risch, D. Birnbaum, Y. Takei, C.H. Fan, L.A. James, E.M. Ladenburger, P. Laurent, G. von Beust, T.K. Mohandas, H. Kobayashi, E. Burt, K. Wiesmeijer, M. Kai, A. Baldini, P. Eydoux, F.C. Canavez, F. Pelliccia, A. Geurts van Kessel, Déborah Bourc'his, S.-H. Park, S. Sebastian, C. Dobkin, R. Stanyon, R.A. Kastelein, L. Langbein, R. Toder, K. Okui, O.L. Serov, N. Matas, M.R. Koehler, R. Moyzis, J.F. Bazan, M.A. van Kuijck, A. Simons, P. Miniou, Y. Yokoyama, D. Molina Gomes, L. Xu, M.A.M. Moreira, H. Kim, E. Sim, J. Ragoussis, F. Saito-Ohara, M. Kool, N. Miyasaka, T. Katagiri, P. Bosco, X. Estivill, N. Archidiacono, G. Novelli, R. Knippers, P. Maccarone, J. Wienberg, M.-J. Pébusque, H.S. Tenenhouse, M. Nadal, W. Schwaeble, H. Hameister, H. van Bokhoven, T. Takahashi, E.I.B. Peerschke, V. Jurecic, X.-L. Yao, Y. Hey, P. Riegman, S.N. Malchenko, H.X. Deng, A.B. Spurdle, N. Hoggard
Publikováno v:
Cytogenetic and Genome Research. 77:I-IV
Autor:
E. Viegas-Péquignot, Véronique Baud, Stephanie L. Chissoe, Bruce A. Roe, Van Cong Nguyen, Marc Lipinski, Sylvie Diriong
Publikováno v:
Genomics. 26:334-344
Proteins with seven transmembrane segments (7TM) define a superfamily of receptors (7TM receptors) sharing the same topology: an extracellular N-terminus, three extramembranous loops on either side of the plasma membrane, and a cytoplasmic C-terminal
Autor:
I. Silva Pereira, F. Recillas Targa, E. Viegas-Péquignot, Faycal Bey, H. G. Nothwang, B. Dutrillaux, Klaus Scherrer, Olivier Coux
Publikováno v:
Molecular and General Genetics MGG. :193-205
Monoclonal antibodies demonstrated high conservation during evolution of a prosomal protein of M(r) 27,000 and differentiation--specific expression of the epitope. More than 90% of the reacting antigen was found as a p27K protein in the free messenge
Autor:
Bernard Malfoy, Marc Jeanpierre, Nadja Kokalj-Vokac, E. Viegas-Péquignot, Bernard Dutrillaux, Anna Almeida
Publikováno v:
Cytogenetic and Genome Research. 63:11-15
Azacytidine (ACR) is known to induce uncoiling and somatic association involving the constitutive heterochromatin of human chromosomes 1, 9, 15, and 16 and the Y. These regions are composed of alphoid and classical satellite DNA sequences. Using spec
Autor:
A Aurias, Marc Jeanpierre, Catherine Turleau, E. Viegas-Péquignot, Alain Fischer, M Prieur, F. LeDeist
Publikováno v:
Human Molecular Genetics. 2:731-735
ICF syndrome has been described as the association of variable immunodeficiency, facial anomalies and centromeric heterochromatin instability. Since the chromosome rearrangements seen in cells of ICF patients are reminiscent of the chromosomal change