Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Anton, Emelyanov"'
Autor:
Jace Jones-Tabah, Kathy He, Nathan Karpilovsky, Konstantin Senkevich, Ghislaine Deyab, Isabella Pietrantonio, Thomas Goiran, Yuting Cousineau, Daria Nikanorova, Taylor Goldsmith, Esther del Cid Pellitero, Carol X.-Q. Chen, Wen Luo, Zhipeng You, Narges Abdian, Jamil Ahmad, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Stanley Fahn, Cheryl Waters, Oury Monchi, Yves Dauvilliers, Nicolas Dupré, Irina Miliukhina, Alla Timofeeva, Anton Emelyanov, Sofya Pchelina, Lior Greenbaum, Sharon Hassin-Baer, Roy N. Alcalay, Austen Milnerwood, Thomas M. Durcan, Ziv Gan-Or, Edward A. Fon
Publikováno v:
Molecular Neurodegeneration, Vol 19, Iss 1, Pp 1-21 (2024)
Abstract Background Variants in the CTSB gene encoding the lysosomal hydrolase cathepsin B (catB) are associated with increased risk of Parkinson’s disease (PD). However, neither the specific CTSB variants driving these associations nor the functio
Externí odkaz:
https://doaj.org/article/e2786b44f0ab42b995b54fb1787459cd
Autor:
Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, Eric Yu, Jamil Ahmad, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Cheryl Waters, Oury Monchi, Yves Dauvilliers, Nicolas Dupré, Irina Miliukhina, Alla Timofeeva, Anton Emelyanov, Sofya Pchelina, Lior Greenbaum, Sharon Hassin-Baer, Roy N. Alcalay, Ziv Gan-Or
Publikováno v:
npj Parkinson's Disease, Vol 10, Iss 1, Pp 1-5 (2024)
Abstract Previous studies have established that rare biallelic SYNJ1 mutations cause autosomal recessive parkinsonism and Parkinson’s disease (PD). We analyzed 8165 PD cases, 818 early-onset-PD (EOPD, 20) in the Sac1 SYNJ1 domain and PD (Pfdr = 0.0
Externí odkaz:
https://doaj.org/article/0ec195e276c84eb0a0914dc2c12af9bb
Autor:
Tatiana S. Usenko, Alla Timofeeva, Mariia Beletskaia, Katerina Basharova, Galina Baydakova, Anastasia Bezrukova, Maria Grunina, Anton Emelyanov, Irina Miliukhina, Ekaterina Zakharova, Sofya Pchelina
Publikováno v:
Journal of Integrative Neuroscience, Vol 23, Iss 1, p 16 (2024)
Background: Mutations in the glucocerebrosidase (GBA1) and leucine-rich repeat kinase 2 (LRRK2) genes, encoding lysosomal enzyme glucocerebrosidase (GCase) and leucine-rich repeat kinase 2 (LRRK2), respectively, are the most common related to Parkins
Externí odkaz:
https://doaj.org/article/fb400ae7883f4d0a87ec3b5710fb5f2b
Autor:
Tatiana, Shtam, Stanislav, Naryzhny, Darya, Kulabukhova, Luiza, Garaeva, Konstantin, Senkevich, Sergey, Landa, Elena, Varfolomeeva, Galina, Salogub, Nikolai, Verlov, Arthur, Kopylov, Elena, Zorina, Roman, Kamyshinsky, Tatiana, Usenko, Alexander, Schwarzman, Ekaterina, Zakharova, Anton, Emelyanov, Sofya, Pchelina
Publikováno v:
In European Journal of Medical Genetics November 2020 63(11)
Autor:
Anton Emelyanov, Tatiana Shtam, Roman Kamyshinsky, Luiza Garaeva, Nikolai Verlov, Irina Miliukhina, Anastasia Kudrevatykh, Gaspar Gavrilov, Yulia Zabrodskaya, Sofya Pchelina, Andrey Konevega
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227949 (2020)
Extracellular vesicles (EVs) are membrane-enclosed vesicles which play important role for cell communication and physiology. EVs are found in many human biological fluids, including blood, breast milk, urine, cerebrospinal fluid (CSF), ejaculate, sal
Externí odkaz:
https://doaj.org/article/e57c9e341a0a49539a97afc31e5dfee5
Autor:
Konstantin Senkevich, Eric Yu, Uladzislau Rudakou, Jamil Ahmad, Jennifer Ruskey, Farnaz Asayesh, Dan Spiegelman, Stanley Fahn, Cheryl Waters, Oury Monchi, Yves Dauvilliers, Nicolas Dupre, Irina Miliukhina, Alla Timofeeva, Daria Kulabukhova, Anton Emelyanov, Sofya Pchelina, Lior Greenbaum, Sharon Hassin, Roy Alcalay, Ziv Gan-Or
Publikováno v:
Sunday, April 23.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c340621931c48668307d3ba0d6308d86
https://doi.org/10.1212/wnl.0000000000202466
https://doi.org/10.1212/wnl.0000000000202466
Autor:
Konstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, Eric Yu, Jamil Ahmad, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Stanley Fahn, Cheryl Waters, Oury Monchi, Yves Dauvilliers, Nicolas Dupré, Lior Greenbaum, Sharon Hassin-Baer, Ilya Nagornov, Alexandr Tyurin, Irina Miliukhina, Alla Timofeeva, Anton Emelyanov, Ekaterina Zakharova, Roy N. Alcalay, Sofya Pchelina, Ziv Gan-Or
Publikováno v:
medRxiv
BackgroundSeveral lysosomal genes are associated with Parkinson’s disease (PD), yet the association between PD andARSA, which encodes for the enzyme arylsulfatase A, remains controversial.ObjectivesTo evaluate the association between rareARSAvarian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9dba04a292b51a9409185c7ba1aacaa
https://europepmc.org/articles/PMC10055435/
https://europepmc.org/articles/PMC10055435/
Autor:
Dmitrii M. Nikolaev, Anton Emelyanov, Vitaly M. Boitsov, Maxim S Panov, Mikhail N. Ryazantsev
Publikováno v:
F1000Research, Vol 6 (2017)
It was demonstrated in recent studies that some rhodopsins can be used in optogenetics as fluorescent indicators of membrane voltage. One of the promising candidates for these applications is archaerhodopsin-3. However, the fluorescent signal for wil
Externí odkaz:
https://doaj.org/article/9d98118d7eaa4757af3afb65a01ca6e3
Autor:
Tatiana Usenko, Anastasia Bezrukova, Katerina Basharova, Alexandra Panteleeva, Mikhail Nikolaev, Alena Kopytova, Irina Miliukhina, Anton Emelyanov, Ekaterina Zakharova, Sofya Pchelina
Table S1: Post-trimming and mapping results to reference genome for all groups, Table S2: Differentially expressed genes from GBA-PD patients compared to controls in monocyte-derived macrophages, Table S3: Differentially expressed genes from GBA-PD p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::558e426de9c25d92c19bd711180f17c1
Autor:
SberDevices, Sberbank, Moscow, Russia, Nadezhda Katricheva, Tatiana Shavrina, Anton Emelyanov, Oleh Shliazhko
Publikováno v:
Computational Linguistics and Intellectual Technologies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e944352dd6a6ad32ae422a8389b91b6
https://doi.org/10.28995/2075-7182-2021-20-204-212
https://doi.org/10.28995/2075-7182-2021-20-204-212