Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Maxim Balasov"'
Publikováno v:
eLife, Vol 10 (2021)
Stimulator of interferon genes (STING) plays an important role in innate immunity by controlling type I interferon response against invaded pathogens. In this work, we describe a previously unknown role of STING in lipid metabolism in Drosophila. Fli
Externí odkaz:
https://doaj.org/article/63bf9e4a64c542be86771e4429ec5e94
Autor:
Katarina Akhmetova, Maxim Balasov, Anton Svitin, Elena Chesnokova, Matthew Renfrow, Igor Chesnokov
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 8, Iss 1, Pp 27-38 (2018)
Septin proteins are polymerizing GTPases that are found in most eukaryotic species. Septins are important for cytokinesis and participate in many processes involving spatial modifications of the cell cortex. In Drosophila, septin proteins Pnut, Sep1,
Externí odkaz:
https://doaj.org/article/4c55346d718b4f24851e8e5323195121
Autor:
Franziska Bleichert, Maxim Balasov, Igor Chesnokov, Eva Nogales, Michael R Botchan, James M Berger
Publikováno v:
eLife, Vol 2 (2013)
In eukaryotes, DNA replication requires the origin recognition complex (ORC), a six-subunit assembly that promotes replisome formation on chromosomal origins. Despite extant homology between certain subunits, the degree of structural and organization
Externí odkaz:
https://doaj.org/article/cb206a238e2245ed96ef6e240768236c
Publikováno v:
Genetics. 216:995-1007
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterized by microtia, primordial dwarfism, small ears and skeletal abnormalities. Patients with MGS often carry mutations in genes encoding the subunits of the Origin Recognition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5fa8995110577626a23433ff6cf8da5
https://doi.org/10.1534/genetics.120.303698
https://doi.org/10.1534/genetics.120.303698
Autor:
Maxim Balasov, Pei-Yuan Qian, Katarina Akhmetova, Haitao Miao, Changdong Liu, Chun Po Fung, To To Choy, Hongyu Yang, Igor Chesnokov, Guang Zhu, Lee Tung Lun, Rahman Ud Din, Honglei Tian, Naining Xu, Yingying You, Bo Zhou, Yanyan Geng, Quan Hao, Xiao Shi, Zhuming Fan
Publikováno v:
Nucleic Acids Research
The six-subunit origin recognition complex (ORC), a DNA replication initiator, defines the localization of the origins of replication in eukaryotes. The Orc6 subunit is the smallest and the least conserved among ORC subunits. It is required for DNA r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcb6f2f0e3d18b47caf7fb325a31a09e
https://doi.org/10.1093/nar/gkaa751
https://doi.org/10.1093/nar/gkaa751
Publikováno v:
Genetics
Meier–Gorlin syndrome (MGS) is a rare, autosomal recessive disorder characterized by microtia, primordial dwarfism, small ears, and skeletal abnormalities. Patients with MGS often carry mutations in genes encoding the subunits of the Origin Recogni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb22eebed389e85a75d6fa9c85831f45
https://pubmed.ncbi.nlm.nih.gov/33037049
https://pubmed.ncbi.nlm.nih.gov/33037049
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterized by microtia, primordial dwarfism, small ears and skeletal abnormalities. Patients with MGS often carry mutations in the genes encoding the subunits of the Origin Recogni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19cfe3d6ff6e1adc665d131b44266b09
https://doi.org/10.1101/2020.04.29.068866
https://doi.org/10.1101/2020.04.29.068866
Autor:
Anton Svitin, Maxim Balasov, Katarina Akhmetova, Elena Chesnokova, Igor Chesnokov, Matthew B. Renfrow
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 8, Iss 1, Pp 27-38 (2018)
Septin proteins are polymerizing GTPases that are found in most eukaryotic species. Septins are important for cytokinesis and participate in many processes involving spatial modifications of the cell cortex. In Drosophila, septin proteins Pnut, Sep1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ba3b6e68533535805681899408999a3
https://doi.org/10.1534/g3.117.300186
https://doi.org/10.1534/g3.117.300186
Publikováno v:
American Journal of Medical Genetics Part A. 167:2533-2540
Meier-Gorlin syndrome (MGS) is an autosomal recessive disorder characterized by microtia, primordial dwarfism, small ears, and skeletal abnormalities. Patients with MGS often carry mutations in the genes encoding the components of the pre-replicative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bf42b626bc44dea5d56c41e52e7a734
https://doi.org/10.1002/ajmg.a.37214
https://doi.org/10.1002/ajmg.a.37214