Search Results - "Couillin, P"

Tumor-Specific Loss of 11p15.5 Alleles in Del11p13 Wilms Tumor and in Familial Adrenocortical Carcinoma by Henry, I., Grandjouan, S., Couillin, P., Barichard, F., Huerre-Jeanpierre, C., Glaser, T., Philip, T., Lenoir, G., Chaussain, J. L., Junien, C.

“…We have compared constitutional and tumor genotypes in nine cases of hereditary Wilms tumor (WT) and in three unrelated cases of familial adrenocortical…”
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Relative positions of two clusters of human alpha-L-fucosyltransferases in 19q (FUT1-FUT2) and 19p (FUT6-FUT3-FUT5) within the microsatellite genetic map of chromosome 19 by Reguigne-Arnould, I, Couillin, P, Mollicone, R, Fauré, S, Fletcher, A, Kelly, R J, Lowe, J B, Oriol, R

“…Five on the seven cloned human fucosyltransferase genes have been mapped to two clusters, one on 19q and the other on 19p. Comparative DNA sequence analysis…”
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A deletion map of the WAGR region on chromosome 11 by Gessler, M, Thomas, G H, Couillin, P, Junien, C, McGillivray, B C, Hayden, M, Jaschek, G, Bruns, G A

“…The WAGR (Wilms tumor, aniridia, genitourinary anomalies, and mental retardation) region has been assigned to chromosome 11p13 on the basis of overlapping…”
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Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic map by Couillin, P, Le Guern, E, Vignal, A, Fizames, C, Ravisé, N, Delportes, D, Reguigne, I, Rosier, M F, Junien, C, van Heyningen, V

“…Using a panel of 25 somatic cell hybrids, we have regionally localized 112 microsatellite markers generated by Généthon and assigned to chromosome 11. A…”
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Natural variation of poliovirus neutralization epitopes by CRAINIC, R, COUILLIN, P, BLONDEL, B, CABAU, N, BOUE, A, HORODNICEANU, F

“…Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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Physical Mapping of 49 Microsatellite Markers on Chromosome 19 and Correlation with the Genetic Linkage Map by Reguigne-Arnould, I., Faure, S., Chery, M., Mota-Vieira, L., Mollicone, R., Candelier, J.J., Oriol, R., Couillin, P.

“…We have regionally localized 49 microsatellite markers developed by Généthon using a panel of previously characterized somatic cell hybrids that retain…”
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Detection by monoclonal antibodies of an antigenic determinant critical for poliovirus neutralization present on VP1 and on heat-inactivated virions by Blondel, B, Akacem, O, Crainic, R, Couillin, P, Horodniceanu, F

“…Hybridoma cell lines were established against poliovirus type 1 (Mahoney) heat-denatured virions (C particles). Each anti-C monoclonal antibody (McAb)…”
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More precise localization of the gene for Hunter syndrome by Le Guern, E, Couillin, P, Oberlé, I, Ravise, N, Boue, J

“…A linkage analysis between the Hunter syndrome locus (IDS) and four polymorphic loci of the Xq27-Xq28 region, DXS105, DXS98, DXS304, and DXS52, was performed…”
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Molecular genetics of alpha-L-fucosyltransferase genes (H, Se, Le, FUT4, FUT5 and FUT6) by Mollicone, R, Candelier, J J, Reguigne, I, Couillin, P, Fletcher, A, Oriol, R

“…Six human alpha-L-fucosyltransferase genes have been registered in the GDB as FUT1 to FUT6 according to the chronology of their description. FUT1 and FUT2…”
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Human Chromosome 16 Encodes a Factor Involved in Induction of Class II Major Histocompatibility Antigens by Interferon γ by Bono, M. R., Alcaide-Loridan, C., Couillin, P., Letouze, B., Grisard, M. C., Jouin, H., Fellous, M.

“…Interferon γ (IFN-γ) induces expression of class II major histocompatibility complex (MHC)-encoded antigens in immunocompetent cells. To gain further insight…”
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First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination by MORNET, E, BOUE, J, RAUX-DEMAY, M, COUILLIN, P, OURY, J. F, DUMEZ, Y, DAUSSET, J, COHEN, D, BOUE, A

“…The close genetic linkage between the gene for congenital adrenal hyperplasia due to 21-hydroxylase (21-OH) deficiency and HLA genes allowed us to use the…”
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The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus by Boehm, T, Lavenir, I, Forster, A, Wadey, R B, Cowell, J K, Harbott, J, Lampert, F, Waters, J, Sherrington, P, Couillin, P

“…A breakpoint cluster region (T-ALLbcr) has been previously described on 11p13 for T-ALL carrying t(11;14)(p13;q11). One further T-ALL breakpoint is described…”
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Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13: subdivision of the WAGR complex region by COUILLIN, P, AZOULAY, M, VAN HEYNINGEN, V, JUNIEN, C, HENRY, I, RAVISE, N, GRISARD, M. C, JEANPIERRE, C, BARICHARD, F, METEZEAU, P, CANDELIER, J. J, LEWIS, W

“…The short arm of chromosome 11 carries genes involved in malformation syndromes, including the aniridia/genitourinary abnormalities/mental retardation (WAGR)…”
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Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluid by Gueux, B, Fiet, J, Couillin, P, Raux-Demay, M C, Mornet, E, Galons, H, Villette, J M, Boue, J, Dreux, C

“…Amniotic fluid levels of 21-deoxycortisol (21-DOF) and 17-hydroxyprogesterone (17-OHP) were measured in 49 pregnancies, including 31 pregnancies at risk for…”
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Chromosomal Localization of Human Genes Governing the Interferon-Induced Antiviral State by Chany, C., Vignal, M., Couillin, P., Van Cong, Nguyen, Boue, J., Boue, A.

“…Interferon sensitivity of different normal and aneusomic human cells and of different mouse-human hybrids cells has been compared. G21 trisomic cells are more…”
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Chromosome 11q localization of one of the three expected genes for the human alpha-3-fucosyltransferases, by somatic hybridization by Couillin, P, Mollicone, R, Grisard, M C, Gibaud, A, Ravisé, N, Feingold, J, Oriol, R

“…Seventy-one human x mouse hybrid cell lines were used to map the locus of a human alpha-3-fucosyltransferase to 11q. The enzyme transfers fucose onto H type 2…”
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Demonstration of human kidney differentiation antigens with monoclonal antibodies by Candelier, JJ, Couillin, P, Bellon, G, Le Pendu, J, Eydoux, P, Boue, A

“…Six human differentiation antigens (EE24.6, EG9.11, EG14.1, EI16.1, EK8.1, EK17.1) have been defined using monoclonal antibodies obtained from mice immunized…”
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Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes by Raux-Demay, M, Mornet, E, Boue, J, Couillin, P, Oury, J F, Ravise, N, Deluchat, C, Boue, A

“…The results of early prenatal diagnoses of congenital adrenal hyperplasia are reported. The determination of 17-hydroxyprogesterone values in amniotic fluid…”
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Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13 by Lavedan, C, Barichard, F, Azoulay, M, Couillin, P, Molina Gomez, D, Nicolas, H, Quack, B, Rethoré, M O, Noel, B, Junien, C

“…We describe a family in whom the phenotypically normal father carries a balanced insertional translocation, ins(14;11)(q23;p12p14). This individual fathered…”
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Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency by MORNET, E, COUILLIN, P, RAUX, M. C, WHITE, P. C, COHEN, D, BOUE, A, DAUSSET, J

“…DNAs from unrelated healthy individuals and unrelated individuals affected with 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) were…”
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