Search Results - "GRISARD, M. C"

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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Parental origin and mechanisms of formation of three cases of 12p tetrasomy by Turleau, C, Simon-Bouy, B, Austruy, E, Grisard, M C, Lemaire, F, Molina-Gomes, D, Siffroi, J P, Boué, J

“…Pallister-Killian syndrome is a clinically recognizable syndrome characterized by tissue-limited mosaicism for an extra 12p isochromosome. Very little is known…”
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Molecular analysis of a ring chromosome X in a family with fragile X syndrome by MORNET, E, BOGYO, A, DELUCHAT, C, SIMON-BOUY, B, MATHIEU, M, THEPOT, F, GRISARD, M.-C, LEGUERN, E, BOUE, J, BOUE, A

“…The phenotypically normal sister of a patient affected by fragile X syndrome was referred for genetic counselling and was found to carry a mosaic karyotype…”
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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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The gene for catalase is assigned between the antigen loci MIC4 and MIC11 by Couillin, P, Azoulay, M, Metezeau, P, Grisard, M C, Junien, C

“…Genetic analysis of the cells of a WAGR patient (W, predisposition to Wilms tumor; A, aniridia; G, genitourinary abnormalities; R, mental retardation), bearing…”
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Characterization of human IFN-γ response using somatic cell hybrids of hematopoietic and nonhematopoietic origin by BONO, M. R, BENECH, P, COUILLIN, P, ALCAIDE-LORIDAN, C, GRISARD, M. C, JOUIN, H, FISCHER, D. G, FELLOUS, M

“…A panel of 27 rodent-human somatic cell hybrids composed of cells of hematopoietic (nonadherent cells) and nonhematopoietic origin (adherent cells) was used to…”
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Molecular studies of a translocated (X;22) DiGeorge patient using somatic cell hybridization by Couillin, P, Zucman, J, Le Guern, E, Reguigne, I, Grisard, M C, Delattre, O, Novelli, G, Dallapiccola, B, Boué, A

“…In order to better characterize the chromosomic rearrangement of an unbalanced 45XX t(X;22) (q28;q11) DiGeorge patient, a somatic hybrid clone segregating the…”
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Strategy for constructing somatic hybrids isolating the two derivative chromosomes in X;autosome translocations. Application to a female patient t(X;5) with Hunter syndrome by Couillin, P, Le Guern, E, Ravise, N, Grisard, M C, Oostra, B A, Boue, A

“…X; autosomal translocations are excellent tools for genetic analysis because of the easy selection of clones isolating the derivative bearing the HPRT gene in…”
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HLA-A, B, C, DR alleles in congenital adrenal hyperplasia by Couillin, P, Kottler-Missonnier, M L, Grisard, M C, Hors, J, Feingold, J, Boué, J, Boué, A

“…HLA markers (A, B, C, DR loci) were determined for the members of 52 unrelated families with at least one child suffering from congenital adrenal hyperplasia…”
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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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HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population by Couillin, P, Rappaport, R, Kuttenn, F, Canlorbe, P, Hors, J, Marcelli-Barge, A, Feingold, J, Grisard, M C, Boué, J, Boué, A

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Characterization of human IFN-? response using somatic cell hybrids of hematopoietic and nonhematopoietic origin by Bono, M. R., Benech, P., Couillin, P., Alcaide-Loridan, C., Grisard, M. C., Jouin, H., Fischer, D. G., Fellous, M.

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Methodology for HLA typing of amniotic fluid fetal cells (author's transl) by Couillin, P, Nicolas, H, Grisard, M C, Boué, J, Boué, A

“…Determination of HLA antigens can be used for prenatal diagnosis of some congenital anomalies such as adrenal hyperplasia (21-hydroxylase deficiency). This…”
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