Search Results - "SUAREZ, H. G"

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    High prevalence of activating ret proto-oncogene rearrangements, in thyroid tumors from patients who had received external radiation by BOUNACER, A, WICKER, R, CAILLOU, B, CAILLEUX, A. F, SARASIN, A, SCHLUMBERGER, M, SUAREZ, H. G

    Published in Oncogene (01-09-1997)
    “…A high frequency (about 60%) of ret rearrangements in papillary thyroid carcinomas of children exposed to radioactive fallout in Belarus after the Chernobyl…”
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    Iodide symporter gene expression in human thyroid tumors by ARTURI, F, RUSSO, D, SCHLUMBERGER, M, DU VILLARD, J.-A, CAILLOU, B, VIGNERI, P, WICKER, R, CHIEFARI, E, SUAREZ, H. G, FILETTI, S

    “…Expression of the Na+/I- symporter (NIS) gene was investigated by RT-PCR in a selected series of 26 primary thyroid carcinomas (19 papillary, 5 follicular, and…”
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    Search for NTRK1 proto-oncogene rearrangements in human thyroid tumours originated after therapeutic radiation by BOUNACER, A, SCHLUMBERGER, M, WICKER, R, DU-VILLARD, J. A, CAILLOU, B, SARASIN, A, SUAREZ, H. G

    Published in British journal of cancer (2000)
    “…Rearrangements of NTRK1 proto-oncogene were detected in 'spontaneous' papillary thyroid carcinomas with a frequency varying from 5 to 25% in different studies…”
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    Association of RET codon 691 polymorphism in radiation-induced human thyroid tumours with C-cell hyperplasia in peritumoural tissue by BOUNACER, A, DU VILLARD, J. A, WICKER, R, CAILLOU, B, SCHLUMBERGER, M, SARASIN, A, SUAREZ, H. G

    Published in British journal of cancer (17-06-2002)
    “…The RET proto-oncogene encodes a protein structurally related to transmembrane receptors with an intracellular tyrosine kinase domain. In human thyroid gland,…”
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    Activating mutations of the TSH receptor in differentiated thyroid carcinomas by Russo, D, Arturi, F, Schlumberger, M, Caillou, B, Monier, R, Filetti, S, Suárez, H G

    Published in Oncogene (02-11-1995)
    “…A series of 14 thyroid carcinomas, characterized for their basal adenyl cyclase activity (ACA), was examined for the presence of activating point mutations in…”
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    Role of the cAMP and MAPK pathways in the transformation of mouse 3T3 fibroblasts by a TSHR gene constitutively activated by point mutation by DU VILLARD, J. A, WICKER, R, CRESPO, P, RUSSO, D, FILETTI, S, GUTKIND, J. S, SARASIN, A, SUAREZ, H. G

    Published in Oncogene (05-10-2000)
    “…Constitutive activating mutations of the TSHR gene, have been detected in about 30 per cent of hyperfunctioning human thyroid adenomas and in a minority of…”
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    Thyrotropin receptor gene alterations in thyroid hyperfunctioning adenomas by RUSSO, D, ARTURI, F, SUAREZ, H. G, SCHLUMBERGER, M, DU VILLARD, J.-A, CROCETTI, U, FILETTI, S

    “…Forty-four thyroid autonomously hyperfunctioning adenomas were analyzed to assess the frequency of mutations occurring in the TSH receptor (TSHR)…”
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    Pattern of ras and gsp oncogene mutations in radiation-associated human thyroid tumors by Challeton, C, Bounacer, A, Du Villard, J A, Caillou, B, De Vathaire, F, Monier, R, Schlumberger, M, Suárez, H G

    Published in Oncogene (03-08-1995)
    “…The preferential activation of the Ki-ras oncogene in follicular radiation-associated human thyroid carcinomas, has been suggested by Wright et al. (1991)…”
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    gsp mutations in human thyroid tumours by Suarez, H G, du Villard, J A, Caillou, B, Schlumberger, M, Parmentier, C, Monier, R

    Published in Oncogene (01-04-1991)
    “…The presence of gsp mutations at codons 201 and 227 in the gene coding for the alpha subunit of the GTP-binding Gs protein which stimulates adenylyl cyclase…”
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    Impaired DNA repair as assessed by the "comet" assay in patients with thyroid tumors after a history of radiation therapy: a preliminary study by Leprat, F, Alapetite, C, Rosselli, F, Ridet, A, Schlumberger, M, Sarasin, A, Suarez, H G, Moustacchi, E

    “…Patients with a history of head and neck irradiation in childhood are at risk to develop thyroid tumors. The aim of this study was to determine if an…”
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    Oncogenic rearrangements of the ret proto-oncogene in thyroid tumors induced after exposure to ionizing radiation by Bounacer, A., Wicker, R., Schlumberger, M., Sarasin, A., Suárez, H.G.

    Published in Biochimie (01-10-1997)
    “…A high frequency (≃ 60%) of ret rearrangements in Chernobyl papillary thyroid c, reinomas (PTC) has been reported recently. The data suggested that the…”
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    Absence of sodium/iodide symporter gene mutations in differentiated human thyroid carcinomas by Russo, D, Manole, D, Arturi, F, Suarez, H G, Schlumberger, M, Filetti, S, Derwahl, M

    Published in Thyroid (New York, N.Y.) (01-01-2001)
    “…Decrease or loss of the sodium iodide (Na+/I-) symporter (NIS) activity influences the suitability of using radioiodine to detect and treat metastatic thyroid…”
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    Detection of activated ras oncogenes in human thyroid carcinomas by Suárez, H G, Du Villard, J A, Caillou, B, Schlumberger, M, Tubiana, M, Parmentier, C, Monier, R

    Published in Oncogene (01-04-1988)
    “…Focus formation following DNA transfection of mouse 3T3-Vill cells was used to search for the presence of activated oncogenes in human thyroid tumors…”
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    Activated oncogenes in human tumors by Suárez, H G

    Published in Anticancer research (01-09-1989)
    “…The search for the genetic targets responsible for tumorigenesis has led to the identification of a number of cancer genes or cellular oncogenes (c-oncogenes)…”
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    Presence of mutations in all three ras genes in human thyroid tumors by Suarez, H G, du Villard, J A, Severino, M, Caillou, B, Schlumberger, M, Tubiana, M, Parmentier, C, Monier, R

    Published in Oncogene (01-04-1990)
    “…Polymerase chain reaction (PCR) amplification followed by oligonucleotide probing was used to investigate the presence of ras genes mutations in human thyroid…”
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    Activated oncogenes in human skin tumors from a repair-deficient syndrome, xeroderma pigmentosum by SUAREZ, H. G, DAYA-GROSJEAN, L, SCHLAIFER, D, NARDEUX, P, RENAULT, G, BOS, J. L, SARASIN, A

    Published in Cancer research (Chicago, Ill.) (01-03-1989)
    “…The recessive autosomal hereditary disease, xeroderma pigmentosum (XP), is characterized by a high incidence of tumors in sun-exposed skin. The defect in early…”
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