Search Results - "Bignon, J"

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    Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis by Férec, C, Raguénès, O, Salomon, R, Roche, C, Bernard, J P, Guillot, M, Quéré, I, Faure, C, Mercier, B, Audrézet, M P, Guillausseau, P J, Dupont, C, Munnich, A, Bignon, J D, Le Bodic, L

    Published in Journal of medical genetics (01-03-1999)
    “…Hereditary pancreatitis (HP) is a rare inherited disorder, characterised by recurrent episodes of pancreatitis often beginning in early childhood. The mode of…”
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    Major oncogenes and tumor suppressor genes involved in epithelial ovarian cancer (review) by Aunoble, B, Sanches, R, Didier, E, Bignon, Y J

    Published in International journal of oncology (01-03-2000)
    “…Ovarian cancer remains the leading cause of death from gynecologic malignancy in Western countries. This cancer results from a succession of genetic…”
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    Synthesis and evaluation of hybrid molecules targeting the vinca domain of tubulin by Gherbovet, O, Sánchez-Murcia, Pedro A, García Alvarez, M C, Bignon, J, Thoret, S, Gago, F, Roussi, F

    Published in Organic & biomolecular chemistry (14-03-2015)
    “…Some hybrids of vinca alkaloids and phomopsin A, linked by a glycine pattern, have been synthesized in one or two steps, by an insertion reaction and shown to…”
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    Report of a family segregating mutations in both the APC and MSH2 genes: juvenile onset of colorectal cancer in a double heterozygote by Uhrhammer, N., Bignon, Y.-J.

    “…Background and aims Mutations in DNA mismatch repair genes are associated with high risk of digestive malignancies [hereditary non-polyposis colorectal cancer…”
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    Inhibition of BRCA1 leads to increased chemoresistance to microtubule-interfering agents, an effect that involves the JNK pathway by LAFARGE, Stéphane, SYLVAIN, Valérie, FERRARA, Marc, BIGNON, Yves-Jean

    Published in Oncogene (04-10-2001)
    “…We have developed ribozymes (Rz) that inhibit BRCA1 expression in order to study the role of this gene in chemosensitivity. Two Rz, targeting positions 358 or…”
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    DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis by Esteller, M, Fraga, M F, Guo, M, Garcia-Foncillas, J, Hedenfalk, I, Godwin, A K, Trojan, J, Vaurs-Barrière, C, Bignon, Y J, Ramus, S, Benitez, J, Caldes, T, Akiyama, Y, Yuasa, Y, Launonen, V, Canal, M J, Rodriguez, R, Capella, G, Peinado, M A, Borg, A, Aaltonen, L A, Ponder, B A, Baylin, S B, Herman, J G

    Published in Human molecular genetics (15-12-2001)
    “…Cancer cells have aberrant patterns of DNA methylation including hypermethylation of gene promoter CpG islands and global demethylation of the genome. Genes…”
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    The regulatory role of the tetrapeptide AcSDKP in skin and hair physiology and the prevention of ageing effects in these tissues - a potential cosmetic role by Hajem, N., Chapelle, A., Bignon, J., Pinault, A., Liu, J.-M., Salah-Mohellibi, N., Lati, E., Wdzieczak-Bakala, J.

    Published in International journal of cosmetic science (01-06-2013)
    “…Synopsis The naturally occurring tetrapeptide acetyl‐N‐Ser‐Asp‐Lys‐Pro (AcSDKP) recognized as a potent angiogenic factor was shown recently to contribute to…”
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    The effects of lycopene on the proliferation of human breast cells and BRCA1 and BRCA2 gene expression by Chalabi, N, Le Corre, L, Maurizis, J-C, Bignon, Y-J, Bernard-Gallon, D.J

    Published in European journal of cancer (1990) (01-07-2004)
    “…The purpose of this study was to demonstrate the effects of lycopene, the major tomato carotenoid, on the expression of the BRCA1 and BRCA2 genes in three…”
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    The Hereditary Pancreatitis Gene Maps to Long Arm of Chromosome 7 by Le Bodic, Louis, Bignon, Jean-Denis, Raguénès, Odile, Mercier, Bernard, Georgelin, Thierry, Schnee, Mathieu, Soulard, François, Gagne, Katia, Bonneville, Françoise, Muller, Jean-Yves, Bachner, Lucien, Férec, Claude

    Published in Human molecular genetics (01-04-1996)
    “…Hereditary pancreatitis (HP) is an autosomal dominant disorder with incomplete penetrance characterized by recurring episodes of severe abdominal pain often…”
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    A Nonsense Mutation in the Hedgehog Receptor CDON Associated With Pituitary Stalk Interruption Syndrome by Bashamboo, A, Bignon-Topalovic, J, Rouba, H, McElreavey, K, Brauner, R

    “…Background: Pituitary stalk interruption syndrome (PSIS) and holoprosencephaly (HPE) are congenital midline defects. Rare mutations in the sonic hedgehog (SHH)…”
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    Resveratrol increases BRCA1 and BRCA2 mRNA expression in breast tumour cell lines by FUSTIER, P, LE CORRE, L, CHALABI, N, VISSAC-SABATIER, C, COMMUNAL, Y, BIGNON, Y-J, BERNARD-GALLON, D. J

    Published in British journal of cancer (07-07-2003)
    “…The phytochemical resveratrol, found in grapes, berries and peanuts, has been found to possess cancer chemopreventive effects by inhibiting diverse cellular…”
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    Comparison of dysplasia profiles in stimulated ovaries and in those with a genetic risk for ovarian cancer by Dauplat, J, Chene, G, Pomel, C, Dauplat, M.M, Bouëdec, G.Le, Mishellany, F, Lagarde, N, Bignon, Y.J, Jaffeux, P, Aublet-Cuvelier, B, Dechelotte, P, Pouly, J.L, Penault-Llorca, F

    Published in European journal of cancer (1990) (01-11-2009)
    “…Abstract Aim Ovarian epithelial dysplasia (OED) was first described after prophylactic oophorectomy for genetic risk of ovarian cancer. In light of Fathalla’s…”
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    Regulation of the Acetoin Catabolic Pathway Is Controlled by Sigma L in Bacillus subtilis by Ali, N O, Bignon, J, Rapoport, G, Debarbouille, M

    Published in Journal of Bacteriology (01-04-2001)
    “…Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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    Asbestos: Scientific Developments and Implications for Public Policy by Mossman, B. T., Bignon, J., Corn, M., Seaton, A., Gee, J. B. L.

    “…Asbestos is a commercial term for a group of fibrous minerals often associated with the development of pulmonary interstitial fibrosis (asbestosis), lung…”
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    Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease by Santt, O., Baranova, H., Albuisson, E., Bignon, Y.-J., Lucotte, G.

    Published in European journal of neurology (01-04-2004)
    “…The present study was conducted to examine the interaction between cytochrome P450 2D6: CYP2D6 (phase I) poor metabolizer (PM) and glutathione S‐transferase…”
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