Polyakova Ekaterina Aleksandrovna. Результативность работы. Персональная страница сотрудника КФУ. Казанский (Приволжский) федеральный университет.
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Polyakova Ekaterina Aleksandrovna (архив)
Полякова Екатерина Александровна
2022
Количественное определение кольцевых фрагментов ДНК Т-и-В-клеточного рецептора TREC/KREC у пациентов с атаксией-телеангиоэктазией с мутацией в гене ATM /Полякова Е. А., Гурьянова И. Е., Шарапова С. О., Сакович И. С., Купчинская А.Н., Алешкевич С. Н., Жаранкова Ю. С., Белевцев М. В. // Иммунопатология, аллергология инфектология. –2022. – №2 –С.6-11.
Statya_po_ATM_Vitebsk.pdf
Statya_po_ATM_Vitebsk.pdf
F_Statya_po_ATM_Vitebsk.pdf
Neutrophil function and adaptive immune system abnormalities in LAD I and LAD III deficient patients / Sakovich Inga S., Polyakova E., Pashchenko O.E., Iritsian S., Hilfanova A., Bondarenko A.V., Boyarchyk O.R., Vakhlyarskaya S.S., Gankovskaya L.V., Prokofjeva T., Belevtsev M., Volokha A. P., Zabara D., Kupchinskaya A.N., Mareika Y. E., Minakovskaya N.V., Kondratenko I. V., Aleinikova O.V., Sharapova S.O. // Abstract book. 20th biennial meeting of the European Society for Immunodeficiencies. – 2022. – PD041
F_ESID_2022___Abstract_Book.pdf
Slavic founder mutation p.S44R in IL7RA gene in children with postmortem diagnosis severe combined immunodeficiency /Polyakova E.A., Sakovich I.S., Geier Ch. B., Leiss-P. A., Kupchinskaya A.N.1, Kostuchenko L.V., Migas A. A., Rozhko O.N., Hilfanova A. M., Mikhalevskaya T.M., Kugeiko T.B., Belevtsev M.V., Naumchik I.V., Golovatya E.I. Prebushenia O. V., Boyarchyk O. R., Hariyan T., Varabyou D.S., O.V. Aleinikova, Lisuk P. N., Dudash P. I., Walter J.E., Sharapova S.O // Abstract book. 20th biennial meeting of the European Society for Immunodeficiencies. – 2022. – PD273
F_ESID_2022___Abstract_Bookw.pdf
Poster: New case of CDC42 deficiency with additional pathogenic variants in UNC13D and DNAH8 Genes / Sakovich I., Kupchinskaya A., Zharankova Yu., Aleshkevich S., Shman T.,, Polyakova E., Tarasova F., Ermilova T., Belevtsev M., Sharapova S. // 20th biennial meeting of the European Society for Immunodeficiencies. – 2022. – PD282
ESID22_ePoster_CDC42.pdf
Poster: Malignancy and chromosome instability syndromes /Volodashchik T. P., Sharapova S. O.1, Aleshkevich S.N., Zharankova Y.S., Polyakova E.A., Guryanova I. E., Belevtsev M.V. // // 20th biennial meeting of the European Society for Immunodeficiencies. – 2022. – PD312
F_ESID22_ePoster_Volodashchik.pdf
Poster: Neutrophil function and adaptive immune system abnormalities in LAD I and LAD III deficient patients / Sakovich Inga S., Polyakova E., Pashchenko O.E., Iritsian S., Hilfanova A., Bondarenko A.V., Boyarchyk O.R., Vakhlyarskaya S.S., Gankovskaya L.V., Prokofjeva T., Belevtsev M., Volokha A. P., Zabara D., Kupchinskaya A.N., Mareika Y. E., Minakovskaya N.V., Kondratenko I. V., Aleinikova O.V., Sharapova S.O. // 20th biennial meeting of the European Society for Immunodeficiencies. – 2022. – PD041
F_ESID22_ePoster_LAD.pdf
Poster: Lymphoproliferation at the onset of PID patients in the Republic of Belarus poster display 07: genetics diagnostics / Zharankova Yu., Volodashchik T.,, Aleshkevich S.,Polyakova E., I.Guryanova I., Yulia Skibo Y.,Belevtsev M. // A 20th biennial meeting of the European Society for Immunodeficiencies. – 2022. – PD348
ESID_2022_Poster_Portrait_Zharankova.pdf
Poster: Slavic founder mutation p.S44R in IL7RA gene in children with postmortem diagnosis severe combined immunodeficiency
F_ESID_2022__Polyakova_Poster_Portrait.pdf
2021
Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene /Guryanova, I., Suffritti, C., Parolin, D. et al. Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene// Clin Mol Allergy 19, 3 (2021). https://doi.org/10.1186/s12948-021-00141-0
s12948_021_00141_0__1_.pdf
Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and NBN Founder Variant c.657_661del5 /Sharapova SO, Pashchenko OE, Bondarenko AV, Vakhlyarskaya SS, Prokofjeva T, Fedorova AS, Savchak I, Mareika Y, Valiev TT, Popa A, Tuzankina IA, Vlasova EV, Sakovich IS, Polyakova EA, Rumiantseva NV, Naumchik IV, Kulyova SA, Aleshkevich SN, Golovataya EI, Minakovskaya NV, Belevtsev MV, Latysheva EA, Latysheva TV, Beznoshchenko AG, Akopyan H, Makukh H, Kozlova O, Varabyou DS, Ballow M, Ong M-S, Walter JE, Kondratenko IV, Kostyuchenko LV and Aleinikova OV //Front. Immunol. 11:602482. doi: 10.3389/fimmu.2020.602482
F_fimmu_11_602482.pdf
F_fimmu_11_602482.pdf
2020
Malignancy and chromosome instability syndromes /Volodashchik T. P., Sharapova S. O.1, Aleshkevich S.N., Zharankova Y.S., Polyakova E.A., Guryanova I. E., Belevtsev M.V. // 20th biennial meeting of the European Society for Immunodeficiencies. – 2022. – PD312
ESID22_ePoster_Volodashchik.pdf
Neutrophil function and adaptive immune system abnormalities in LAD I and LAD III deficient patients / Sakovich Inga S., Polyakova E., Pashchenko O.E., Iritsian S., Hilfanova A., Bondarenko A.V., Boyarchyk O.R., Vakhlyarskaya S.S., Gankovskaya L.V., Prokofjeva T., Belevtsev M., Volokha A. P., Zabara D., Kupchinskaya A.N., Mareika Y. E., Minakovskaya N.V., Kondratenko I. V., Aleinikova O.V., Sharapova S.O. // Abstract book. 20th biennial meeting of the European Society for Immunodeficiencies. – 2022. – PD041
ESID22_ePoster_LAD.pdf
ESID22_ePoster_LAD.pdf
2019
Постер
F_Polyakova_ATM.jpg
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https://scholar.google.com/citations?user=oWB-G9sAAAAJ&hl=en
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