Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sarmi Nath"'
Autor:
Rebecca M. Jones, Joaquin Herrero Ruiz, Shaun Scaramuzza, Sarmi Nath, Chaoyu Liu, Marta Henklewska, Toyoaki Natsume, Robert G. Bristow, Francisco Romero, Masato T. Kanemaki, Agnieszka Gambus
Publikováno v:
iScience, Vol 27, Iss 7, Pp 110260- (2024)
Summary: To ensure timely duplication of the entire eukaryotic genome, thousands of replication machineries (replisomes) act on genomic DNA at any time during S phase. In the final stages of this process, replisomes are unloaded from chromatin. Unloa
Externí odkaz:
https://doaj.org/article/1301c90532be429a8d1333f2902214f5
Autor:
Sarmi Nath, Ganesh Nagaraju
Publikováno v:
PLoS Genetics, Vol 16, Iss 4, p e1008701 (2020)
FANCJ helicase mutations are known to cause hereditary breast and ovarian cancers as well as bone marrow failure syndrome Fanconi anemia. FANCJ plays an important role in the repair of DNA inter-strand crosslinks and DNA double-strand breaks (DSBs) b
Externí odkaz:
https://doaj.org/article/b69c18ae1a83417bb6515ca20b60407a
Autor:
Rebecca M. Jones, Joaquin Herrero Ruiz, Shaun Scaramuzza, Sarmi Nath, Marta Henklewska, Toyoaki Natsume, Francisco Romero, Masato T. Kanemaki, Agnieszka Gambus
To ensure faultless duplication of the entire genome, eukaryotic replication initiates from thousands of replication origins. Replication forks emanating from origins move through the chromatin until they encounter forks from neighbouring origins, at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::893a3589aad5aad8d1ad84656be02df0
https://doi.org/10.1101/2022.07.12.499744
https://doi.org/10.1101/2022.07.12.499744
Autor:
Ganesh Nagaraju, Sarmi Nath
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 16, Iss 4, p e1008701 (2020)
PLoS Genetics, Vol 16, Iss 4, p e1008701 (2020)
FANCJ helicase mutations are known to cause hereditary breast and ovarian cancers as well as bone marrow failure syndrome Fanconi anemia. FANCJ plays an important role in the repair of DNA inter-strand crosslinks and DNA double-strand breaks (DSBs) b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c28da09c1f46594bf0bcf7e30f8b369c
https://pubmed.ncbi.nlm.nih.gov/32251466
https://pubmed.ncbi.nlm.nih.gov/32251466
Publikováno v:
Nucleic Acids Research
The FANCJ DNA helicase is linked to hereditary breast and ovarian cancers as well as bone marrow failure disorder Fanconi anemia (FA). Although FANCJ has been implicated in the repair of DNA double-strand breaks (DSBs) by homologous recombination (HR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c121e6b46908ca373725dbd0d469d4c
https://pubmed.ncbi.nlm.nih.gov/28911102
https://pubmed.ncbi.nlm.nih.gov/28911102
Autor:
Shreya Banerjee, Sarita Gupta, Gitika Kharkwal, Jatin Machhi, Ragitha Chruvattil, Sarmi Nath, Mange Ram Yadav
Publikováno v:
Molecular neurobiology. 54(9)
Elevated levels of glucocorticoid, a steroid hormone released in response to stress, have been implicated in the pathophysiology of diabetes, which is now known to extend its effect on brain functions. Hence, we aimed to investigate the status of bra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55f9a66f60f7a1be504d41bd198fdb47
https://pubmed.ncbi.nlm.nih.gov/27822713
https://pubmed.ncbi.nlm.nih.gov/27822713