日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Induction of Premature Cell Senescence Stimulated by High Doses of Antioxidants Is Mediated by Endoplasmic Reticulum Stress

高剂量抗氧化剂刺激细胞过早衰老的诱导是由内质网应激介导的

期刊:International Journal of Molecular Sciences
影响因子:0.7
doi:10.3390/ijms222111851
Olga Lyublinskaya, Julia Kornienko, Julia Ivanova, Natalia Pugovkina, Larisa Alekseenko, Ekaterina Lyublinskaya, Irina Tyuryaeva, Irina Smirnova, Tatiana Grinchuk, Mariia Shorokhova, Anna Krasnenko, Nikolay Plotnikov, Nikolay Nikolsky
免疫
细胞生物学
其它细胞
Senescence
发表日期：2021
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Apremilast Pharmacogenomics in Russian Patients with Moderate-to-Severe and Severe Psoriasis

阿普米司特在俄罗斯中重度及重度银屑病患者中的药物基因组学研究

期刊:Journal of Personalized Medicine
影响因子:3
doi:10.3390/jpm11010020
Verbenko, Dmitry A; Karamova, Arfenya E; Artamonova, Olga G; Deryabin, Dmitry G; Rakitko, Alexander; Chernitsov, Alexandr; Krasnenko, Anna; Elmuratov, Artem; Solomka, Victoria S; Kubanov, Alexey A
银屑病
发表日期：2020
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Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report

俄罗斯女性癫痫伴智力障碍患者中发现两例新的PCDH19基因突变：病例报告

期刊:BMC Medical Genetics
影响因子:
doi:10.1186/s12881-020-01119-6
Kozina, Anastasiya Aleksandrovna; Okuneva, Elena Grigorievna; Baryshnikova, Natalia Vladimirovna; Fedonyuk, Inessa Dmitrievna; Kholin, Alexey Aleksandrovich; Il'ina, Elena Stepanovna; Krasnenko, Anna Yurievna; Stetsenko, Ivan Fedorovich; Plotnikov, Nikolay Alekseevich; Klimchuk, Olesia Igorevna; Surkova, Ekaterina Ivanovna; Ilinsky, Valery Vladimirovich
CDH1
癫痫
神经科学
发表日期：2020
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Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report

俄罗斯某家族中由上皮钠通道 (ENaC) γ 亚基新突变引起的利德尔综合征：病例报告

期刊:BMC Nephrology
影响因子:2.4
doi:10.1186/s12882-019-1579-4
Kozina, Anastasiya A; Trofimova, Tatiana A; Okuneva, Elena G; Baryshnikova, Natalia V; Obuhova, Varvara A; Krasnenko, Anna Yu; Tsukanov, Kirill Yu; Klimchuk, Olesya I; Surkova, Ekaterina I; Shatalov, Peter A; Ilinsky, Valery V
发表日期：2019
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Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report

POMGNT1复合杂合突变导致A3型肌营养不良-肌糖蛋白病：病例报告

期刊:BMC Pediatrics
影响因子:2
doi:10.1186/s12887-019-1470-2
Borisovna, Kondakova Olga; Yurievna, Krasnenko Anna; Yurievich, Tsukanov Kirill; Igorevna, Klimchuk Olesya; Olegovich, Korostin Dmitriy; Igorevna, Davidova Anna; Timofeevna, Batysheva Tatyana; Vyacheslavovna, Zhurkova Natalia; Ivanovna, Surkova Ekaterina; Alekseevich, Shatalov Peter; Vladimirovich, Ilinsky Valery
MGN
发表日期：2019
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A novel elastin gene frameshift mutation in a Russian family with cutis laxa: a case report

俄罗斯一个患有皮肤松弛症的家族中发现一种新的弹性蛋白基因移码突变：病例报告

期刊:BMC Dermatology
影响因子:
doi:10.1186/s12895-019-0084-6
Okuneva, E G; Kozina, A A; Baryshnikova, N V; Krasnenko, A Yu; Tsukanov, K Yu; Klimchuk, O I; Surkova, E I; Ilinsky, V V
发表日期：2019
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A novel MFSD8 mutation in a Russian patient with neuronal ceroid lipofuscinosis type 7: a case report

俄罗斯一名患有7型神经元蜡样脂褐质沉积症的患者中发现一种新的MFSD8突变：病例报告

期刊:BMC Medical Genetics
影响因子:
doi:10.1186/s12881-018-0669-7
Kozina, Anastasiya Aleksandrovna; Okuneva, Elena Grigorievna; Baryshnikova, Natalia Vladimirovna; Krasnenko, Anna Yurievna; Tsukanov, Kirill Yurievich; Klimchuk, Olesya Igorevna; Kondakova, Olga Borisovna; Larionova, Anna Nikolaevna; Batysheva, Tatyana Timofeevna; Surkova, Ekaterina Ivanovna; Shatalov, Peter Alekseevich; Ilinsky, Valery Vladimirovich
神经科学
发表日期：2018
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Molecular Genetic Analysis of Human Endometrial Mesenchymal Stem Cells That Survived Sublethal Heat Shock

对亚致死热休克后存活的人类子宫内膜间充质干细胞进行分子遗传学分析

期刊:Stem Cells International
影响因子:3.3
doi:10.1155/2017/2362630
Vinogradov, A E; Shilina, M A; Anatskaya, O V; Alekseenko, L L; Fridlyanskaya, I I; Krasnenko, A; Kim, A; Korostin, D; Ilynsky, V; Elmuratov, A; Tsyganov, O; Grinchuk, T M; Nikolsky, N N
细胞生物学
发育与干细胞
Human
干细胞
发表日期：2017
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