Search Results - "Levanat, S."

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    PO-155 Therapeutic evaluation of HEDGEHOG-GLI signalling pathway through miRNA and mRNA profiling of ovarian carcinoma by Levanat, S, Ozretic, P, Hackl, H, Plattner, C, Trnski, D, Sabol, M, Kalafatic, D, Musani, V

    Published in ESMO open (01-07-2018)
    “…IntroductionSignalling pathway Hedgehog-Gli (Hh-Gli) is involved in embryonal ovarian development, but its atypical activation can lead to different types of…”
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    PO-149 Expression profiling of TP53, TP73, NME and GLI families of genes/proteins in metastatic melanoma by Ozretić, P, Hanžić, N, Trnski, D, Proust, B, Radić, M, Sabol, M, Milas, I, Bosnar, M Herak, Levanat, S, Slade, N

    Published in ESMO open (01-07-2018)
    “…IntroductionMalignant melanoma is the most aggressive form of skin cancer and resistant to available therapies, therefore new molecular approaches for better…”
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    Characterization of the c.190T>C missense mutation in BRCA1 codon 64 (Cys64Arg) by WILLEMS, P, MAGRI, V, VANDERSICKEL, V, PERLETTI, G, VRAL, A, CRETNIK, M, FASANO, M, JAKUBOWSKA, A, LEVANAT, S, LUBINSKI, J, MARRAS, E, MUSANI, V, THIERENS, H

    Published in International journal of oncology (01-04-2009)
    “…In the Milan area (Northern Italy), we identified a family characterized by a high prevalence of ovarian and breast cancer cases (5 out of 6 subjects, over 3…”
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    PTCH gene altered in dentigerous cysts by Pavelić, B., Levanat, S., Crnić, I., Kobler, P., Anić, I., Manojlović, S., Šutalo, J.

    Published in Journal of oral pathology & medicine (01-10-2001)
    “…: Motivated by the evidence that odontogenic keratocysts are associated with genetic alterations, we examined the possibility that development of other…”
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    A two-hit model for developmental defects in Gorlin syndrome by Levanat, Sonja, Gorlin, Robert J, Fallet, Shari, Johnson, Dennis R, Fantasia, John E, Bale, Alien E

    Published in Nature genetics (01-01-1996)
    “…Many birth defects that are rare in the general population duster in families. A two-hit mechanism, similar to Knudson's model for neoplasia, could explain…”
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    Aberration of FHIT gene is associated with increased tumor proliferation and decreased apoptosis-clinical evidence in lung and head and neck carcinomas by Pavelić, K, Krizanac, S, Cacev, T, Hadzija, M P, Radosević, S, Crnić, I, Levanat, S, Kapitanović, S

    Published in Molecular medicine (Cambridge, Mass.) (01-07-2001)
    “…Human FHIT (fragile histidine triad) gene is highly conserved gene homologous to a group of genes identified in prokaryotes and eukaryotes. Loss of FHIT…”
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    Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients by SHIMKETS, R, GAILANI, M. R, SIU, V. M, YANG-FENG, T, PRESSMAN, C. L, LEVANAT, S, GOLDSTEIN, A, DEAN, M, BALE, A. E

    Published in American journal of human genetics (01-08-1996)
    “…Gorlin syndrome is an autosomal dominant disorder characterized by multiple basal cell carcinomas, medulloblastomas, ovarian fibromas, and a variety of…”
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