Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Daniela Farchi"'
Autor:
Priya Kapoor-Vazirani, Sandip K. Rath, Xu Liu, Zhen Shu, Nicole E. Bowen, Yitong Chen, Ramona Haji-Seyed-Javadi, Waaqo Daddacha, Elizabeth V. Minten, Diana Danelia, Daniela Farchi, Duc M. Duong, Nicholas T. Seyfried, Xingming Deng, Eric A. Ortlund, Baek Kim, David S. Yu
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-18 (2022)
SAMHD1 has a dNTPase-independent resection function in genome maintenance. Here the authors show that SAMHD1 is deacetylated at conserved K354 by SIRT1 to facilitate direct binding with ssDNA to promote DNA end resection and homologous recombination.
Externí odkaz:
https://doaj.org/article/28cc02127faa4de9bf5e662150744115
Autor:
Maria C Sterrett, Daniela Farchi, Sarah E Strassler, Lawrence H Boise, Milo B Fasken, Anita H Corbett
Publikováno v:
G3 Genes|Genomes|Genetics.
The RNA exosome is a conserved molecular machine that processes/degrades numerous coding and non-coding RNAs. The 10-subunit complex is composed of three S1/KH cap subunits (human EXOSC2/3/1; yeast Rrp4/40/Csl4), a lower ring of six PH-like subunits
Autor:
Maria C. Sterrett, Daniela Farchi, Sarah E. Strassler, Lawrence H. Boise, Milo B. Fasken, Anita H. Corbett
The RNA exosome is a conserved molecular machine that processes/degrades numerous coding and non-coding RNAs. The 10-subunit complex is composed of three S1/KH cap subunits (human EXOSC2/3/1; yeast Rrp4/40/Csl4), a lower ring of six PH-like subunits
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::249c5be31d88688ff5c17567619962b1
https://doi.org/10.1101/2022.10.31.514520
https://doi.org/10.1101/2022.10.31.514520
Autor:
Sara W. Leung, Richard Baker, Richard S. Lee, Sarah E. Strassler, Munira A. Basrai, Liz Enyenihi, Laurie Hess, Elise S. Withers, Isaac Kremsky, Maria C. Sterrett, Anita H. Corbett, Milo B. Fasken, Daniela Farchi, Ambro van Hoof
Publikováno v:
RNA. 27:1046-1067
RNA exosomopathies, a growing family of diseases, are linked to missense mutations in genes encoding structural subunits of the evolutionarily conserved, 10-subunit exoribonuclease complex, the RNA exosome. This complex consists of a three-subunit ca
Autor:
Maria C, Sterrett, Liz, Enyenihi, Sara W, Leung, Laurie, Hess, Sarah E, Strassler, Daniela, Farchi, Richard S, Lee, Elise S, Withers, Isaac, Kremsky, Richard E, Baker, Munira A, Basrai, Ambro, van Hoof, Milo B, Fasken, Anita H, Corbett
Publikováno v:
RNA
RNA exosomopathies, a growing family of diseases, are linked to missense mutations in genes encoding structural subunits of the evolutionarily conserved, 10-subunit exoribonuclease complex, the RNA exosome. This complex consists of a three-subunit ca
Autor:
Maria C. Sterrett, Liz Enyenihi, Sara W. Leung, Laurie Hess, Sarah E. Strassler, Daniela Farchi, Richard S. Lee, Elise S. Withers, Isaac Kremsky, Richard E. Baker, Munira A. Basrai, Ambro van Hoof, Milo B. Fasken, Anita H. Corbett
RNA exosomopathies, a growing family of tissue-specific diseases, are linked to missense mutations in genes encoding the structural subunits of the conserved 10-subunit exoribonuclease complex, the RNA exosome. Such mutations in the cap subunit gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbff2b129e62f025530ef4f7c2747a73
https://doi.org/10.1101/2020.12.06.413658
https://doi.org/10.1101/2020.12.06.413658