Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Joanna Rusecka"'
Publikováno v:
Frontiers in Genetics, Vol 10 (2020)
RNase H1 is able to recognize DNA/RNA heteroduplexes and to degrade their RNA component. As a consequence, it has been implicated in different aspects of mtDNA replication such as primer formation, primer removal, and replication termination, and sig
Externí odkaz:
https://doaj.org/article/3d338694f9804c249bd874c1702d6e08
Publikováno v:
Postępy Biochemii. 64:300-303
Choroby mitochondrialne wynikają z nieprawidłowej funkcji mitochondrialnego systemu fosforylacji oksydacyjnej: łańcucha oddechowego i syntazy ATP, produkującego energię komórkową w formie ATP. Jest to zróżnicowana grupa chorób dziedzicznyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57bc064f55281a8509dd32f6c95a386a
https://doi.org/10.18388/pb.2018_143
https://doi.org/10.18388/pb.2018_143
Autor:
Anna Kostera-Pruszczyk, Joanna Rusecka, Joanna Kosińska, Ewa Bartnik, Biruta Kierdaszuk, Magdalena Kaliszewska, Katarzyna Tońska, Anna Kamińska
Publikováno v:
Genes
Volume 12
Issue 1
Genes, Vol 12, Iss 54, p 54 (2021)
Volume 12
Issue 1
Genes, Vol 12, Iss 54, p 54 (2021)
Mitochondrial encephalomyopathies comprise a group of heterogeneous disorders resulting from impaired oxidative phosphorylation (OxPhos). Among a variety of symptoms progressive external ophthalmoplegia (PEO) seems to be the most common. The aim of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f5e9eb9fa21a47ae74a18085f3fdcc0
Publikováno v:
Frontiers in Genetics, Vol 10 (2020)
RNase H1 is able to recognize DNA/RNA heteroduplexes and to degrade their RNA component. As a consequence, it has been implicated in different aspects of mtDNA replication such as primer formation, primer removal, and replication termination, and sig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf50152488733847cd147ac6d4ad5788
https://www.frontiersin.org/article/10.3389/fgene.2019.01393/full
https://www.frontiersin.org/article/10.3389/fgene.2019.01393/full
Publikováno v:
Journal of Applied Genetics
Mitochondrial diseases are defined by a respiratory chain dysfunction and in most of the cases manifest as multisystem disorders with predominant expression in muscles and nerves and may be caused by mutations in mitochondrial (mtDNA) or nuclear (nDN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcf097c6d9ee21dcd8d3b0bfe54044d4
https://doi.org/10.1007/s13353-017-0424-3
https://doi.org/10.1007/s13353-017-0424-3
Publikováno v:
Frontiers in Genetics
RNase H1 is able to recognize DNA/RNA heteroduplexes and to degrade their RNA component. As a consequence, it has been implicated in different aspects of mtDNA replication such as primer formation, primer removal, and replication termination, and sig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::927ec0fe78c650e9b20b6985e7824112
https://pubmed.ncbi.nlm.nih.gov/32082360
https://pubmed.ncbi.nlm.nih.gov/32082360
Publikováno v:
Postepy biochemii. 64(4)
Mitochondrial diseases are caused by dysfunction of the mitochondrial oxidative phosphorylation system and can be the result of mutations both in mitochondrial DNA and in nuclear DNA. Mitochondrial diseases collectively describe a diverse group of he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7471d24fc97f6c51ca0f3c03f276510c
https://pubmed.ncbi.nlm.nih.gov/30656914
https://pubmed.ncbi.nlm.nih.gov/30656914