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    1.
    0562680 - FZÚ 2023 RIV US eng J - Journal Article
    Aad, G. - Abbott, B. - Abbott, D.C. - Chudoba, Jiří - Hejbal, Jiří - Hladík, Ondřej - Jačka, Petr - Kepka, Oldřich - Kroll, Jiří - Kupčo, Alexander - Latoňová, Věra - Lokajíček, Miloš - Lysák, Roman - Marčišovský, Michal - Mikeštíková, Marcela - Němeček, Stanislav - Penc, Ondřej - Šícho, Petr - Staroba, Pavel - Svatoš, Michal - Taševský, Marek … Total 2884 authors
    Measurements of the Higgs boson inclusive and differential fiducial cross-sections in the diphoton decay channel with pp collisions at √s = 13 TeV with the ATLAS detector.
    Journal of High Energy Physics. Roč. 2022, č. 8 (2022), č. článku 027. ISSN 1029-8479. E-ISSN 1029-8479
    Research Infrastructure: CERN-CZ II - 90104; e-INFRA CZ - 90140
    Institutional support: RVO:68378271
    Keywords : Hadron-Hadron Scattering * Higgs physics * p p: colliding beams
    OECD category: Particles and field physics
    Impact factor: 5.4, year: 2022
    Method of publishing: Open access
    Permanent Link: https://hdl.handle.net/11104/0336470
    FileDownloadSizeCommentaryVersionAccess
    0562680.pdf13.6 MBCC licencePublisher’s postprintopen-access
     
     
    2.
    0463462 - ÚOCHB 2017 RIV US eng J - Journal Article
    Bolar, N. A. - Golzio, C. - Živná, M. - Hayot, G. - Van Hemelrijk, C. - Schepers, D. - Vandeweyer, G. - Hoischen, A. - Huyghe, J. R. - Raes, A. - Matthys, E. - Sys, E. - Azou, M. - Gubler, M. C. - Praet, M. - Van Camp, G. - McFadden, K. - Pediaditakis, I. - Přistoupilová, A. - Hodaňová, K. - Vyleťal, P. - Hartmannová, H. - Stránecký, V. - Hůlková, H. - Barešová, V. - Jedličková, I. - Sovová, J. - Hnízda, Aleš - Kidd, K. - Bleyer, A. J. - Spong, R. S. - Vande Walle, J. - Mortier, G. - Brunner, H. - Van Laer, L. - Kmoch, S. - Katsanis, N. - Loeys, B. L.
    Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia.
    American Journal of Human Genetics. Roč. 99, č. 1 (2016), s. 174-187. ISSN 0002-9297. E-ISSN 1537-6605
    R&D Projects: GA MŠMT(CZ) LO1304
    Institutional support: RVO:61388963
    Keywords : Sec61 * tubulo-interstitial kidney disease * rare disease
    Subject RIV: EB - Genetics ; Molecular Biology
    Impact factor: 9.025, year: 2016
    http://www.sciencedirect.com/science/article/pii/S0002929716301999
    Permanent Link: http://hdl.handle.net/11104/0262678
     
     

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