Search Results - "Lepaslier, Denis"

Cloning of a Gene (RIG-G) Associated with Retinoic Acid-Induced Differentiation of Acute Promyelocytic Leukemia Cells and Representing a New Member of a Family of Interferon-Stimulated Genes by Yu, Man, Tong, Jian-Hua, Mao Mao, Kan, Li-Xin, Liu, Meng-Min, Sun, Yi-Wu, Fu, Gang, Jing, Yong-Kui, Yu, Long, Lepaslier, Denis, Lanotte, Michel, Wang, Zhen-Yi, Chen, Zhu, Waxman, Samuel, Wang, Ya-Xin, Tan, Jia-Zhen, Chen, Sai-Juan

“…In a cell line (NB4) derived from a patient with acute promyelocytic leukemia, all-trans-retinoic acid (ATRA) and interferon (IFN) induce the expression of a…”
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Physical Mapping and Genomic Structure of the HumanTNFR2Gene by Beltinger, Christian P., White, Peter S., Maris, John M., Sulman, Erik P., Jensen, Sanford J., LePaslier, Denis, Stallard, Barbara J., Goeddel, David V., de Sauvage, Frederic J., Brodeur, Garrett M.

“…The tumor necrosis factor receptor 2 (TNFR2) gene localizes to 1p36.2, a genomic region characteristically deleted in neuroblastomas and other malignancies. In…”
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Physical mapping and genomic structure of the human TNFR2 gene by BELTINGER, C. P, WHITE, P. S, MARIS, J. M, SULMAN, E. P, JENSEN, S. J, LEPASLIER, D, STALLARD, B. J, GOEDDEL, D. V, DE SAUVAGE, F. J, BRODEUR, G. M

“…The tumor necrosis factor receptor 2 (TNFR2) gene localizes to 1p36. 2, a genomic region characteristically deleted in neuroblastomas and other malignancies…”
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Carbonic anhydrase II (CA II) deficiency in Maghrebian patients : evidence for founder effect and genomic recombination at the CA II locus by FATHALLAH, D. M, BEJAOUI, M, LEPASLIER, D, CHATER, K, SLY, W. S, DELLAGI, K

“…A splice junction mutation at the exon 2-intron 2 boundary of the carbonic anhydrase II (CA II) gene was previously shown to be the unique mutation underlying…”
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Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbands by Colleaux, L, May, M, Belougne, J, Lepaslier, D, Schwartz, C, Fontes, M

“…Genetic studies in families with X linked mental retardation have suggested the location of several MR genes in the human q21 region. Since the establishment…”
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Sequence polymorphism of HLA-DP beta chains by LEE, J. S, SARTORIS, S, BRIATA, P, CHOI, E, CULLEN, C, LEPASLIER, D, YUNIS, I

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Characterization and chromosomal assignment of yeast artificial chromosomes containing human 3p13-p21-specific sequence tagged sites by Michaelis, Susanne C., Bardenheuer, Walter, Lux, Andreas, Schramm, Alexander, Gockel, Anja, Siebert, Reiner, Willers, Christoph, Schmidtke, Katja, Todt, Birgit, van der Hout, Annemarie H., Buys, Charles H.C.M., Heppell-Parton, Amanda C., Rabbitts, Pamela H., Ungar, Sylvia, Smith, David, LePaslier, Denis, Cohen, Daniel, Opalka, Bertram, Schütte, Jochen

“…Human chromosomal region 3p12–p23 is proposed to harbor at least three tumor suppressor genes involved in the development of lung cancer, renal cell carcinoma,…”
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