Zheglo Diana - Research Centre for Medical Genetics

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论文共 13 篇作者统计合作学者相似作者

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Replication stress causes delayed mitotic entry and chromosome 12 fragility at the ANKS1B large neuronal gene in human induced pluripotent stem cells

Anastasiia V. Kislova,Diana Zheglo,Victoria O. Pozhitnova, Philipp S. Sviridov, Elmira P. Gadzhieva,Ekaterina S. Voronina

Research Square (Research Square)no. 3 (2023): 1-16

引用1浏览0WOS引用

Pattern of chromosomal aberrations persisting over 30 years in a Chernobyl Nuclear Power Plant accident survivor: study using mFISH

Victoriya Nikitina,Vladimir Nugis, Tatiyana Astrelina,Diana Zheglo,Irina Kobzeva, Mariya Kozlova, Irina Galstyan,Elena Lomonosova,Aliy Zhanataev, Tatiyana Karaseva,Alexander S Samoylov

JOURNAL OF RADIATION RESEARCH（2022）

引用3浏览0WOS引用

Search for markers and mechanisms of resistance to TKI therapy

Elmira P. Adilgereeva,Alex G. Nikitin,Diana G. Zheglo,Oleg A. Shukhov,Svetlana A. Smirnikhina,Alexander V. Lavrov,Ekaterina Y. Chelysheva,Anna G. Turkina,Sergey I. Kutsev

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Generation of induced pluripotent stem cell line (RCMGi008-A) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/CFTRdele2.3 mutations in CFTR gene

Ekaterina Kondrateva,Irina Panchuk,Anna Demchenko,Olga Grigorieva,Diana Zheglo,Ekaterina Voronina,Anastasija Erofeeva,Vyacheslav Tabakov,Maria Orlova,Alexander Lavrov,Svetlana Smirnikhina,Sergey Kutsev

Stem Cell Research（2022）

引用1浏览0WOS引用

Variants In The Asxl1 And > For Dmnt3a Genes May Provide A Personalized Approach To Targeted Cml Therapy

E. P. Adilgereeva,A. G. Nikitin,D. G. Zheglo,O. A. Shukhov, S. A. Smirnikhina,E. Y. Chelysheva,A. V. Lavrov,A. G. Turkina,S. I. Kutsev

EUROPEAN JOURNAL OF HUMAN GENETICS（2020）

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Variants in the ASXL1 and DMNT3A genes are potential markers of the effectiveness of tyrosine kinase inhibitors therapy in chronic myeloid leukemia

Э.П. Адильгереева,А.Г. Никитин,Д.Г. Жегло,О.А. Шухов, С.А. Смирнихина, Е.Ю. Челышева,А.В. Лавров,А.Г. Туркина, С.И. Куцев

Nauchno-prakticheskii zhurnal «Medicinskaia genetika»pp.88-89, (2020)

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The FRA14B common fragile site maps to a region prone to somatic and germline rearrangements within the large GPHN gene

Diana Zheglo,Lena M Brueckner, Olga Sepman,Elisa M Wecht, Ekaterina Kuligina, Evgenij Suspitsin, Evgenij Imyanitov,Larissa Savelyeva

GENES CHROMOSOMES & CANCER（2019）

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Toxic and DNA damaging effects of a functionalized fullerene in human embryonic lung fibroblasts

E S Ershova,V A Sergeeva, A I Chausheva,D G Zheglo,V A Nikitina,T D Smirnova, L V Kameneva,L N Porokhovnik,S I Kutsev,P A Troshin, I I Voronov,E A Khakina,

Mutation research. Genetic toxicology and environmental mutagenesis（2016）

引用32浏览0WOS引用

Genotoxicity of Single-Walled Carbon Nanotubes: In Vitro Study on Human Embryonic Fibroblast Cells

V. A. Nikitina, A. I. Chausheva,I. A. Suetina, L. D. Katosova,D. G. Zheglo,M. V. Mezentseva, V. I. Platonova,Yu. A. Revazova,S. I. Kutsev

Bulletin of experimental biology and medicine（2015）

引用4浏览0WOS引用

Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats

Lena M. Brueckner,Evgeny Sagulenko,Elisa M. Hess,Diana Zheglo,Anne Blumrich,Manfred Schwab,Larissa Savelyeva

Human genetics（2012）

引用13浏览0WOS引用

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