Search Results - "Huret, J L"

Atlas of Genetics and Cytogenetics in Oncology and Haematology, year 2003 by Huret, Jean-Loup, Dessen, Philippe, Bernheim, Alain

“…The ‘Atlas of Genetics and Cytogenetics in Oncology and Haematology’ (http://www.infobiogen.fr/services/chromcancer) contains concise and updated cards on…”
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CD30-positive large cell lymphomas ('Ki-1 lymphoma') are associated with a chromosomal translocation involving 5q35 by Mason, D Y, Bastard, C, Rimokh, R, Dastugue, N, Huret, J L, Kristoffersson, U, Magaud, J P, Nezelof, C, Tilly, H, Vannier, J P

“…A chromosomal translocation involving a breakpoint on the long arm of chromosome 5 at position q35 has been reported previously in 17 cases of neoplasia. In 14…”
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AML1 overexpression and or mutations should be checked in trisomy 21 patients with megakaryocytic leukemia by Huret, J L, Léonard, C

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Atlas of genetics and cytogenetics in oncology and haematology, an interactive database by Huret, J L, Minor, S L, Dorkeld, F, Dessen, P, Bernheim, A

“…The 'Atlas of Genetics and Cytogenetics in Oncology and Haematology' (http://www.infobiogen.fr/services/chromcancer ) is a database devoted to chromosome…”
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Atlas of Genetics and Cytogenetics in Oncology and Haematology, updated by Huret, J L, Dessen, P, Bernheim, A

“…The 'Atlas of Genetics and Cytogenetics in Oncology and Haematology' (http://www.infobiogen.fr/services/chromcancer) is an Internet database aimed at genes…”
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An Atlas on genes and chromosomes in oncology and haematology by Huret, J L, Senon, S, Bernheim, A, Dessen, P

“…The "Atlas of Genetics and Cytogenetics in Oncology and Haematology" http://www.infobiogen.fr/services/chromcancer is a peer-reviewed and free internet…”
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Monosomy 21q: two cases of del(21q) and review of the literature by Huret, J L, Léonard, C, Chery, M, Philippe, C, Schafei-Benaissa, E, Lefaure, G, Labrune, B, Gilgenkrantz, S

“…We report on two cases of partial monosomy 21 and review cases with a partial or an apparently full monosomy 21. In situ hybridization and/or molecular studies…”
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Eleven new cases of del(9p) and features from 80 cases by Huret, J L, Leonard, C, Forestier, B, Rethoré, M O, Lejeune, J

“…We report 11 cases of del(9p) and review 69 previously published ones. Of the 80 cases, 39 have a del(9p) as the sole anomaly. The symptoms are typical and…”
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An atlas of chromosomes in hematological malignancies. Example: 11q23 and MLL partners by Huret, J L, Dessen, P, Bernheim, A

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beta $ Amyloid Gene Duplication in Alzheimer's Disease and Karyotypically Normal down Syndrome by Delabar, Jean-Maurice, Goldgaber, Dmitry, Lamour, Yvon, Nicole, Annie, Huret, Jean-Louis, De Grouchy, Jean, Brown, Paul, Gajdusek, D. Carleton, Sinet, Pierre-Marie

“…With the recently cloned complementary DNA probe, $\lambda $Am4 for the chromosome 21 gene encoding brain amyloid polypeptide ($\beta $ amyloid protein) of…”
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A database on cytogenetics in haematology and oncology by Dorkeld, Franck, Bernheim, Alain, Dessen, Philippe, Huret, Jean-Loup

“…The aim of ‘Atlas of Genetics and Cytogenetics in Oncology and Haematology’ (http://www.infobiogen.fr/services/chromcancer) is to present summarized…”
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Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T-prolymphocytic leukaemia: four new cases and a review of the literature by Mossafa, H, Brizard, A, Huret, J L, Brizard, F, Lessard, M, Guilhot, F, Tanzer, J

“…Cytogenetic abnormalities found in four cases of T-cell prolymphocytic leukaemia (T-PLL) are described. An isochromosome 8q was found in three patients and a…”
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Protocols to establish genotype-phenotype correlations in down syndrome by EPSTEIN, C. J, KORENBERG, J. R, KEMPER, T. L, LOTT, I. T, LUBIN, B. H, MAGENIS, E, OPITZ, J. M, PATTERSON, D, PRIEST, J. H, PUESCHEL, S. M, RAPOPORT, S. I, SINET, P.-M, ANNEREN, G, TANZI, R. E, DE LA CRUZ, F, ANTONARAKIS, S. E, AYME, S, COURCHESNE, E, EPSTEIN, L. B, FOWLER, A, GRONER, Y, HURET, J. L

“…To facilitate the process of making a phenotypic map of Down syndrome, a workshop was sponsored by the National Institute of Child Health and Human Development…”
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Presence of HBV DNA in spermatozoa: a possible vertical transmission of HBV via the germ line by Hadchouel, M, Scotto, J, Huret, J L, Molinie, C, Villa, E, Degos, F, Brechot, C

“…Using molecular hybridization we studied the presence and state of HBV DNA in sperm samples obtained from 17 patients with HBV infection (eight HBsAg chronic…”
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Chromosome 21 and platelets: a gene dosage effect? by Huret, J. L., Léonard, C.

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Cytogenetic heterogeneity in t(11;19) acute leukemia: clinical, hematological and cytogenetic analyses of 48 patients--updated published cases and 16 new observations by Huret, J L, Brizard, A, Slater, R, Charrin, C, Bertheas, M F, Guilhot, F, Hählen, K, Kroes, W, van Leeuwen, E, Schoot, E V

“…We report on 16 cases of t(11;19) acute leukemia and review data of published observations: altogether updated data of 48 patients are analyzed. Four…”
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Complex translocations, simple variant translocations and Ph-negative cases in chronic myelogenous leukaemia by Huret, J L

“…A proportion of cases of chronic myelogenous leukaemia (CML) has been described either (1) with a variant translocation, or (2) without the apparent…”
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Nuclear chromatin decondensation of human sperm: a review by Huret, J L

“…The decondensation of the nucleus of human spermatozoa normally occurs in the oocyte and allows the formation of a male pronucleus. This phenomenon must occur…”
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Malignant Histiocytosis: A Specific t(2;5)(p23;q35) Translocation? Review of the Literature by Benz-Lemoine, Elisabeth, Brizard, Andre, Huret, Jean-Loup, Babin, Philippe, Guilhot, Francois, Couet, Dominique, Tanzer, Joseph

“…In this paper, the investigators report a well documented case of malignant histiocytosis (MH) with a t(2;5)(p23;q35) translocation. A breakpoint in 5q35…”
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Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: Clinical assessment by Barnicoat, A J, Bonneau, J L, Boyd, E, Docherty, Z, Fennell, S J, Huret, J L, King, M, Maltby, E L, McManus, S, Pilz, D T, Shafei-Benaissa, E, Super, M, Tolmie, J

“…We report on the clinical and cytogenetic assessment of five cases of Down syndrome phenotype with either a partial duplication of chromosome 21 or a normal…”
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