Hasil Pencarian - Denis Pyankov

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  1. 1
    Case Report: Phenotype-Driven Diagnosis of Atypical Dravet-Like Syndrome Caused by a Novel Splicing Variant in the SCN2A Gene

    Case Report: Phenotype-Driven Diagnosis of Atypical Dravet-Like Syndrome Caused by a Novel Splicing Variant in the SCN2A Gene oleh Artem Sharkov, Artem Sharkov, Peter Sparber, Anna Stepanova, Denis Pyankov, Sergei Korostelev, Mikhail Skoblov

    Diterbitkan 2022-05-01
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  2. 2
    Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas

    Cases report: Mosaic structural variants of the EXT1 gene in previously genetically unconfirmed multiple osteochondromas oleh Artem Borovikov, Andrey Marakhonov, Aysylu Murtazina, Kseniya Davydenko, Alexandra Filatova, Nailya Galeeva, Varvara Kadnikova, Natalya Ogorodova, Daria Gorodilova, Ilya Kanivets, Ilya Kanivets, Denis Pyankov, Konstantin Zherdev, Konstantin Zherdev, Aleksandr Petel’guzov, Pavel Zubkov, Alexander Polyakov, Olga Shchagina, Mikhail Skoblov

    Diterbitkan 2024-08-01
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  3. 3
    Tumor-associated macrophages respond to chemotherapy by detrimental transcriptional reprogramming and suppressing stabilin-1 mediated clearance of EGF

    Tumor-associated macrophages respond to chemotherapy by detrimental transcriptional reprogramming and suppressing stabilin-1 mediated clearance of EGF oleh Irina Larionova, Irina Larionova, Irina Larionova, Artem Kiselev, Elena Kazakova, Elena Kazakova, Tengfei Liu, Marina Patysheva, Marina Patysheva, Pavel Iamshchikov, Pavel Iamshchikov, Quan Liu, Dieuwertje M. Mossel, Vladimir Riabov, Militsa Rakina, Militsa Rakina, Alexey Sergushichev, Natalia Bezgodova, Sergei Vtorushin, Nikolai Litviakov, Nikolai Litviakov, Evgeny Denisov, Philipp Koshkin, Denis Pyankov, Matvei Tsyganov, Marina Ibragimova, Nadezhda Cherdyntseva, Nadezhda Cherdyntseva, Nadezhda Cherdyntseva, Julia Kzhyshkowska, Julia Kzhyshkowska, Julia Kzhyshkowska, Julia Kzhyshkowska

    Diterbitkan 2023-03-01
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