Search Results - "Kerckaert, J.P"

2.105 Transcriptome profiling in peripheral blood cells of LRRK2 G2019S mutation patients by Mutez, E, Mouroux, V, Lepetre, F, Larvor, L, Vanbesien-Mailliot, C, Kerckaert, J.P, Defebvre, L, Destee, A, Chartier-Harlin, M.-C

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Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1 S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease by Jardin, F, Callanan, M, Penther, D, Ruminy, P, Troussard, X, Kerckaert, J P, Figeac, M, Parmentier, F, Rainville, V, Vaida, I, Bertrand, P, Duval, A B, Picquenot, J M, Chaperot, L, Marolleau, J P, Plumas, J, Tilly, H, Bastard, C

“…CD4+CD56+ haematodermic neoplasms (HDN) constitute a rare disease characterized by aggressive clinical behaviour and a poor prognosis. Tumour cells from HDN…”
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Waved aCGH: to smooth or not to smooth by Leprêtre, F, Villenet, C, Quief, S, Nibourel, O, Jacquemin, C, Troussard, X, Jardin, F, Gibson, F, Kerckaert, J.P, Roumier, C, Figeac, M

“…Array-based comparative genomic hybridization (aCGH) is a powerful tool to detect genomic imbalances in the human genome. The analysis of aCGH data sets has…”
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Isolation of a human urinary trypsin inhibitor by Balduyck, M, Hayem, A, Kerckaert, J P, Mizon, C, Mizon, J

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Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1 S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease by Callanan, M, Penther, D, Plumas, J, Vaida, I, Picquenot, J.M, Kerckaert, J.P, Rainville, V, Duval, A.B, Troussard, X, Marolleau, J.P, Tilly, H, Bertrand, P, Figeac, M, Chaperot, L, Bastard, C, Parmentier, F, Jardin, F, Ruminy, P

“…Corrigenda: no abstract…”
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Splicing with inverted order of exons occurs proximal to large introns by Cocquerelle, C., Daubersies, P., Majérus, M.A., Kerckaert, J.P., Bailleul, B.

“…Following our studies which showed that the alpha and beta exons of the chicken c‐ets‐1 gene are not conserved in the human homologue, we succeeded in…”
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Uptake and biological transformation of beta NiS and alpha Ni3S2 by human embryonic pulmonary epithelial cells (L132) in culture by Hildebrand, H F, D'Hooghe, M C, Shirali, P, Bailly, C, Kerckaert, J P

“…The cytotoxicity, biological transformation and interaction with plasma membranes of alpha Ni3S2 and beta NiS were studied on human embryonic pulmonary…”
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Highly simplified analytical or preparative slab gel electrophoresis by Kerckaert, J P

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Sst I RFLP linked to the human ets-1 gene by KERCKAERT, J. P, DOZIER, C, LOUCHEUX-LEFEBVRE, M. H, STEHELIN, D

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Recherche de gènes localisés sur le bras long du chromosome 20 impliqués dans les mécanismes de progression tumorale des cancers coliques humains by Nicolet, C., Guerin, E., Schneider, A., Neuville, A., Kerckaert, J.P., Kedinger, M., Gaub, M.P., Guenot, D.

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Electrophoretic preparation of the two rat α-fetoprotein variants by Kerckaert, J.P., Bayard, B., Quief, S., Biserte, G.

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Purification by affinity chromatography of the solubilized oligosaccharyltransferase from hen oviducts using a privileged secondary structure adopting peptide by Aubert, J P, Chiroutre, M, Kerckaert, J P, Helbecque, N, Loucheux-Lefebvre, M H

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Direct analysis of the lectin reactivity of alpha-fetoprotein in maternal serum by crossed affinity radio-immunoelectrophoresis by Kerckaert, J P, Bayard, B, Puech, F, Codaccioni, X, Biserte, G

“…Affinity experiments with the lentil (Lens culinaris) lectin have revealed the existence of two distinct molecular populations of alpha-fetoprotein: lectin…”
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Molecular cloning and structural analysis of cDNAs that encode 3 small GTP-binding proteins from sugar beet by Dallery, E, Quief, S, Ben Jilany, K E, Kerckaert, J P, Hagège, D

“…Isolation of homologous ras-related genes from sugar beet has never been reported. Screening cDNA library from Beta vulgaris L. Hilma resulted in the isolation…”
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Circular dichroic study of rat alphafetoprotein by Aubert, J.P., Kerckaert, J.P., Bayard, B., Loucheux-Lefebvre, M.H.

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Chronic myeloid leukemia with unusual variant Ph translocation (22;22)(q11;q13). Two cases with chimeric BCR-ABL transcripts by Laï, J L, Aissaoui, Z, Collyn-d'Hooghe, C, Delfau, M H, Grandchamp, B, Fenaux, P, Jouet, J P, Desablens, B, Deminatti, M, Loucheux-Lefebvre, M H

“…We studied two cases of chronic myelogenous leukemia (CML) with unusual variant Philadelphia (Ph) translocation (22;22)(q11;q13). Southern blot analysis showed…”
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