Tsygankova P

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COST Action CA15203 (2016-2021): MitoEAGLE
Evolution-Age-Gender-Lifestyle-Environment: mitochondrial fitness mapping


 

Tsygankova P


MitoPedia topics: EAGLE 

COST: Member


COST WG4: WG4


Name Tsygankova Polina, PhD
Institution Lab metabolic disorders

Research centre for medical genetics

RAMS

Address 115478, MOSKVORECHE 1,
City Moscow
State/Province
Country Russia
Email [email protected]
Weblink
O2k-Network Lab RU Moscow Itkis YS


Labels: Field of research: Basic, Clinical 



Publications

 PublishedReference
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.

Abstracts

 PublishedReference
Krylova 2017 MiPschool Obergurgl2017
KrylovaT.jpg
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.

Participated at


  • Research interests: PDH-deficiency, Alpers syndrome, Leigh syndrome, mitochondrial DNA depletion syndromes