14 results for author:"Besmond C." in Literature citations
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| Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes. Guilmeau S., Niot I., Laigneau J.P., Devaud H., Petit V., Brousse N., Bouvier R., Ferkdadji L., Besmond C., Aggerbeck L.P. et al. Histochem. Cell Biol. 128:115-123(2007) · Mapped (4) |
| Polymorphisms of the receptor of advanced glycation endproducts (RAGE) and the development of nephropathy in type 1 diabetic patients. Prevost G., Fajardy I., Besmond C., Balkau B., Tichet J., Fontaine P., Danze P.M., Marre M. Diabetes Metab. 31:35-39(2005) · Mapped (41) |
| Characterization of a putative type IV aminophospholipid transporter P-type ATPase. Flamant S., Pescher P., Lemercier B., Clement-Ziza M., Kepes F., Fellous M., Milon G., Marchal G., Besmond C. |
| The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis. Gabolde M., Hubert D., Guilloud-Bataille M., Lenaerts C., Feingold J., Besmond C. J. Med. Genet. 38:310-311(2001) · Mapped (50) |
| Genotyping of the three major allelic variants of the human mannose-binding lectin gene by denaturing gradient gel electrophoresis. Gabolde M., Muralitharan S., Besmond C. Hum. Mutat. 14:80-83(1999) · UniProtKB (1) |
| Molecular analysis of the insulin receptor gene for prenatal diagnosis of leprechaunism in two families. Desbois-Mouthon C., Girodon E., Ghanem N., Caron M., Pennerath A., Conteville P., Magre J., Besmond C., Goossens M., Capeau J. et al. Prenat. Diagn. 17:657-663(1997) · UniProtKB (1) |
| Deletion of Asn281 in the alpha-subunit of the human insulin receptor causes constitutive activation of the receptor and insulin desensitization. Desbois-Mouthon C., Sert-Langeron C., Magre J., Oreal E., Blivet M.J., Flori E., Besmond C., Capeau J., Caron M. J. Clin. Endocrinol. Metab. 81:719-727(1996) · UniProtKB (1) |
| A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family. Valverde D., Solans T., Grinberg D., Balcells S., Vilageliu L., Bayes M., Chivelet P., Besmond C., Goossens M., Gonzalez-Duarte R. et al. Hum. Genet. 97:35-38(1996) · UniProtKB (1) |
| Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma. Blanquet V., Turleau C., Gross-Morand M.S., Senamaud-Beaufort C., Doz F., Besmond C. Hum. Mol. Genet. 4:383-388(1995) · UniProtKB (1) |
| Nucleotide sequence of a cDNA clone for human aldolase B. Besmond C., Dreyfus J.-C., Gregori C., Frain M., Zakin M.M., Sala Trepat J., Kahn A. Biochem. Biophys. Res. Commun. 117:601-609(1983) · UniProtKB (1) |
| Molecular cloning of cDNA for rat L-type pyruvate kinase and aldolase B. Simon M.P., Besmond C., Cottreau D., Weber A., Chaumet-Riffaud P., Dreyfus J.C., Trepat J.S., Marie J., Kahn A. J. Biol. Chem. 258:14576-14584(1983) · Mapped (2) |
| Molecular cloning and sequence analysis of cDNA for human transferrin. Uzan G., Frain M., Park I., Besmond C., Maessen G., Trepat J.S., Zakin M.M., Kahn A. Biochem. Biophys. Res. Commun. 119:273-281(1984) · UniProtKB (1) |
| The structural gene for aldolase B (ALDB) maps to 9q13----32. Henry I., Gallano P., Besmond C., Weil D., Mattei M.G., Turleau C., Boue J., Kahn A., Junien C. Ann. Hum. Genet. 49:173-180(1985) · Mapped (3) |
| Dietary and hormonal regulation of aldolase B gene expression. Munnich A., Besmond C., Darquy S., Reach G., Vaulont S., Dreyfus J.C., Kahn A. J. Clin. Invest. 75:1045-1052(1985) · Mapped (2) |