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COST Action CA15203 (2016-2021): MitoEAGLE
Evolution-Age-Gender-Lifestyle-Environment: mitochondrial fitness mapping
Itkis YS
MitoPedia topics: EAGLE
COST: Member
COST WG4: WG4
Name | Itkis Yulya S, PhD |
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Institution | Lab. Metab. Disorders
Research Centre for Medical Genetics RAMS |
Address | Moskvorechie 1, |
City | Moscow |
State/Province | |
Country | Russia |
[email protected] | |
Weblink | |
O2k-Network Lab | RU Moscow Itkis YS |
Labels:
Field of research: Basic, Clinical
Publications
Published | Reference | |
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Itkis 2019 Mitochondrion | 2019 | Itkis Y, Krylova T, Pechatnikova NL, De Grassi A, Tabakov VY, Pierri CL, Aleshin V, Boyko A, Bunik VI, Zakharova EY (2019) A novel variant m.641A>T in the mitochondrial MT-TF gene is associated with epileptic encephalopathy in adolescent. Mitochondrion 47:10-17. |
Krylova 2019 Mitochondrion | 2019 | Krylova TD, Sheremet NL, Tabakov VY, Lyamzaev KG, Itkis YS, Tsygankova PG, Andreeva NA, Shmelkova MS, Nevinitsyna TA, Kadyshev VV, Zakharova EY (2019) Three rare pathogenic mtDNA substitutions in LHON patients with low heteroplasmy. Mitochondrion 50:139-144. |
Krylova 2017 Biomed Khim | 2017 | Krylova TD, Tsygankova PG, Itkis YS, Sheremet NL, Nevinitsyna TA, Mikhaylova SV, Zakharova EY (2017) High resolution respirometry in diagnostic of mitochondrial disorders caused by mitochondrial complex I deficiency. Biomed Khim 63:327-33. |
Sheremet 2016 Biochemistry (Moscow) | 2016 | Sheremet NL, Nevinitsyna TA, Zhorzholadze NV, Ronzina IA, Itkis YS, Krylova TD, Tsygankova PG, Malakhova VA, Zakharova EY, Tokarchuk AV, Panteleeva AA, Karger EM, Lyamzaev KG, Avetisov SE (2016) Previously unclassified mutation of mtDNA m.3472T>C: evidence of pathogenicity in Leberβs hereditary optic neuropathy. Biochemistry (Moscow) BM16-078. |
Abstracts
Published | Reference | |
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Krylova 2017 MiPschool Obergurgl | 2017 | High-resolution respirometry in diagnostic of mitochondrial complex I deficiency. |
Itkis MiP2010 | 2010 | Itkis YS, Rudenskaya GE, Tsygankova PG, Zakharova EY, Mikhailova SV (2010) Rare mitochondrial mutations in cases of Leigh disease. Abstract MiP2010. |
Tsygankova MiP2010 | 2010 | Tsygankova PG, Zakharova EY, Itkis YS, Mikhailova SV, Rudenskaya GE, Dadali EL, Nikolaeva EA (2010) Developing the algorithm for molecular diagnostics of infantile mitochondrial encephalomyopathies. MiP2010. |
Itkis 2010 Abstract IOC60 | 2010 | Itkis YS (2010) Respirometry application in Leigh disease diagnostic and treatment. MiPNet15.10. |