يعرض 1 - 10 نتائج من 370 نتيجة بحث عن '"Baralle FE"', وقت الاستعلام: 0.83s تنقيح النتائج
  1. 1
    Transcriptional control of CHRNA1 gene in thymus by a promoter SNP associated with onset of autoimmune myasthenia gravis

    المؤلفون: Giraud, M, Kyewski, B, Baralle, FE, Vincent, A, Wilicox, N, Beeson, D, Garchon, HJ

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b62cd7b9ec03a7380411b0bfb685e6f2
    https://ora.ox.ac.uk/objects/uuid:afc031e3-32fb-4752-a819-2c24567d6260

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  2. 2
    The primary structure of the human epsilon-globin gene

    المؤلفون: Baralle, FE, Shoulders, CC, Proudfoot, NJ

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7cf54bdc9c01abbfd30210d5b3257b59
    https://ora.ox.ac.uk/objects/uuid:8ff68260-0050-4371-af1f-fad652d1da3f

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  3. 3
    hnRNP H binding at the 5' splice site correlates with the pathological effect of two intronic mutations in the NF-1 and TSHbeta genes

    المؤلفون: BURATTI E, BARALLE M, DE CONTI L, BARALLE D, AYALA YM, BARALLE FE, ROMANO, MAURIZIO

    المساهمون: Buratti, E, Baralle, M, DE CONTI, L, Baralle, D, Romano, Maurizio, Ayala, Ym, Baralle, Fe

    مصطلحات موضوعية: Binding Sites Exons Genetic Predisposition to Disease Hela Cells Heterogeneous-Nuclear Ribonucleoprotein Group F-H/*metabolism Heterogeneous-Nuclear Ribonucleoproteins/metabolism Human Introns Model, beta Subunit/*genetics/metabolism, Genetic Neurofibromin 1/*genetics/metabolism *Point Mutation *RNA Splice Sites *RNA Splicing RNA, Binding Sites Exons Genetic Predisposition to Disease Hela Cells Heterogeneous-Nuclear Ribonucleoprotein Group F-H/*metabolism Heterogeneous-Nuclear Ribonucleoproteins/metabolism Human Introns Models, Messenger/chemistry/metabolism Ribonucleoprotein, U1 Small Nuclear/metabolism Support, Non-U.S. Gov't Thyrotropin

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::de15e03d312630f2cf4855296eb35ef2
    http://hdl.handle.net/11368/1699843

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  4. 4
    Regulation of 3' splice site selection in the 844ins68 polymorphism of the cystathionine Beta -synthase gene

    المؤلفون: ROMANO M, MARCUCCI R, BURATTI E, AYALA YM, BARALLE FE, SEBASTIO, GIANFRANCO

    المساهمون: Romano, M, Marcucci, R, Buratti, E, Ayala, Ym, Sebastio, Gianfranco, Baralle, Fe

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3730::6c9936874904ed52c364adca7f2cfd09
    http://hdl.handle.net/11588/162456

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  5. 5
    Functional characterization of the novel mutation IVS 8 (-11delC) (-14T>A) in the intron 8 of the glucocerebrosidase gene of two Italian siblings with Gaucher disease type I

    المؤلفون: ROMANO, MAURIZIO, DANEK GM, BARALLE FE, MAZZOTTI R, FILOCAMO M.

    المساهمون: Romano, Maurizio, Danek, Gm, Baralle, Fe, Mazzotti, R, Filocamo, M.

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::33e27b5df153179d7cffe368d912cbd0
    http://hdl.handle.net/11368/1717559

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  6. 6
    The A/G polymorphism in the -78 position of the apolipoprotein A-I promoter does not have a direct effect on transcriptional efficiency

    المؤلفون: DANEK GM, VALENTI M, BARALLE FE, ROMANO, MAURIZIO

    المساهمون: Danek, Gm, Valenti, M, Baralle, Fe, Romano, Maurizio

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9b7cc0a469b410042f831606e77992c9
    http://hdl.handle.net/11368/1717497

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  7. 7
    Genetics and molecular biology

    المؤلفون: CATTIN, LUIGI, BARALLE FE

    المساهمون: Cattin, Luigi, Baralle, Fe

    المصدر: Current opinion in lipidology. 8(1)

    مصطلحات موضوعية: Nutrition and Dietetics, Apolipoproteins E, Genotype, Alzheimer Disease, Arteriosclerosis, Risk Factors, Endocrinology, Diabetes and Metabolism, Genetics, Humans, Genetic Predisposition to Disease, Cell Biology, Cardiology and Cardiovascular Medicine, Molecular Biology

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83be9172a264eebb8ca853fcdbf028f4
    https://pubmed.ncbi.nlm.nih.gov/9127715

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  8. 8
    2 POINT MUTATIONS WITHIN THE ADDUCIN GENES ARE INVOLVED IN BLOOD-PRESSURE VARIATION

    المؤلفون: BIANCHI G, TRIPODI G, SALARDI S, BARBER BR, GARCIA R, LEONI P, TORIELLI L, CUSI D, FERRANDI M, PINNA LA, BARALLE FE, FERRARI P., CASARI , GIORGIO NEVIO

    المساهمون: Bianchi, G, Tripodi, G, Casari, GIORGIO NEVIO, Salardi, S, Barber, Br, Garcia, R, Leoni, P, Torielli, L, Cusi, D, Ferrandi, M, Pinna, La, Baralle, Fe, Ferrari, P.

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_____10495::7bfd352f111c9e531b1b5401b268f3a0

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  9. 9
    CLONING, EXPRESSION, AND IMMUNOLOGICAL CHARACTERIZATION OF RECOMBINANT LOLIUM-PERENNE ALLERGEN LOL P-II

    المؤلفون: SIDOLI A, TAMBORINI E, GIUNTINI I, VOLONTE G, PAINI C, DELALLA C, SICCARDI AG, BARALLE FE, GALLIANI S, AROSIO P., LEVI , SONIA MARIA ROSA

    المساهمون: Sidoli, A, Tamborini, E, Giuntini, I, Levi, SONIA MARIA ROSA, Volonte, G, Paini, C, Delalla, C, Siccardi, Ag, Baralle, Fe, Galliani, S, Arosio, P.

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_____10495::b47be20dffef045b0d3a695dee0ed9be

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  10. 10
    New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12

    المؤلفون: Pagani, F Stuani, C Tzetis, M Kanavakis, E Efthymiadou, A Doudounakis, S Casals, T Baralle, FE

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2127::193f3fa8db9dd75d9413e3ef76033936
    https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3083705

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