Itkis YS

From Bioblast
Jump to: navigation, search

e-COST MitoEAGLE countries
News and Events         BEC 2020.1 Mitochondrial physiology         About COST Action MitoEAGLE         Working Groups         MitoEAGLE Summit 2020 Obergurgl AT         Short-Term Scientific Missions         Inclusiveness Target Countries         Management Committee         Members    

COST Action CA15203 MitoEAGLE
Evolution-Age-Gender-Lifestyle-Environment: mitochondrial fitness mapping


Itkis YS

MitoPedia topics: EAGLE 

COST: Member


Name Itkis Yulya S, PhD
Institution Lab. Metab. Disorders

Research Centre for Medical Genetics


Address Moskvorechie 1,
City Moscow
Country Russia
Email [email protected]
O2k-Network Lab RU Moscow Itkis YS

Labels: Field of research: Basic, Clinical 


Itkis 2019 Mitochondrion2019Itkis 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 Mitochondrion2019Krylova 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 Khim2017Krylova 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)2016Sheremet 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 Leber’s hereditary optic neuropathy. Biochemistry (Moscow) BM16-078.


Krylova 2017 MiPschool Obergurgl2017
High-resolution respirometry in diagnostic of mitochondrial complex I deficiency.
Itkis MiP20102010Itkis YS, Rudenskaya GE, Tsygankova PG, Zakharova EY, Mikhailova SV (2010) Rare mitochondrial mutations in cases of Leigh disease. Abstract MiP2010.
Tsygankova MiP20102010Tsygankova 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 IOC602010Itkis YS (2010) Respirometry application in Leigh disease diagnostic and treatment. MiPNet15.10.

Participated at