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Expanding the genetic landscape of congenital neutropenia: CXCR2 mutations in three families revealed through whole exome sequencing.
Haematologica. 2024 Dec 1;109(12):4140-4144. doi: 10.3324/haematol.2024.285569.
Haematologica. 2024.
PMID: 39086298
Free PMC article.
No abstract available.
Dissecting thrombus-directed chemotaxis and random movement in neutrophil near-thrombus motion in flow chambers.
Korobkin JD, Deordieva EA, Tesakov IP, Adamanskaya EA, Boldova AE, Boldyreva AA, Galkina SV, Lazutova DP, Martyanov AA, Pustovalov VA, Novichkova GA, Shcherbina A, Panteleev MA, Sveshnikova AN.
Korobkin JD, et al. Among authors: tesakov ip.
BMC Biol. 2024 May 20;22(1):115. doi: 10.1186/s12915-024-01912-2.
BMC Biol. 2024.
PMID: 38764040
Free PMC article.
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Platelet functional abnormalities in pediatric patients with kaposiform hemangioendothelioma/Kasabach-Merritt phenomenon.
Martyanov AA, Tesakov IP, Khachatryan LA, An OI, Boldova AE, Ignatova AA, Koltsova EM, Korobkin JD, Podoplelova NA, Svidelskaya GS, Yushkova E, Novichkova GA, Eble JA, Panteleev MA, Kalinin DV, Sveshnikova AN.
Martyanov AA, et al. Among authors: tesakov ip.
Blood Adv. 2023 Sep 12;7(17):4936-4949. doi: 10.1182/bloodadvances.2022009590.
Blood Adv. 2023.
PMID: 37307200
Free PMC article.
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Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations.
Ovsyannikova GS, Fedorova DV, Tesakov IP, Martyanov AA, Ignatova AA, Ponomarenko EA, Zharkov PA, Pavlova AV, Raykina EV, Maschan MA, Panteleev MA, Novichkova GA, Sveshnikova AN, Smetanina NS.
Ovsyannikova GS, et al. Among authors: tesakov ip.
Haematologica. 2022 Oct 1;107(10):2511-2516. doi: 10.3324/haematol.2022.281340.
Haematologica. 2022.
PMID: 35796010
Free PMC article.
No abstract available.
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