Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Elise S, Withers"'
Autor:
Laramie D Lemon, Sneha Kannan, Kim Wai Mo, Miranda Adams, Haley G Choi, Alexander O D Gulka, Elise S Withers, Hasset T Nurelegne, Valeria Gomez, Reina E Ambrocio, Rhea Tumminkatti, Richard S Lee, Morris Wan, Milo B Fasken, Jennifer M Spangle, Anita H Corbett
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 12, Iss 7 (2022)
AbstractSomatic missense mutations in histone genes turn these essential proteins into oncohistones, which can drive oncogenesis. Understanding how missense mutations alter histone function is challenging in mammals as mutations occur in a single his
Externí odkaz:
https://doaj.org/article/4d79f600263649b8878492dc6f2abbc7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9676bd9b83a84f217103e157cc78e7c
https://doi.org/10.1261/rna.078618.120
https://doi.org/10.1261/rna.078618.120
Autor:
Kim Wai Mo, Valeria Gomez, Miranda Adams, Anita H. Corbett, Haley G. Choi, Laramie D. Lemon, Richard S. Lee, Reina E. Ambrocio, Milo B. Fasken, Sneha Kannan, Elise S. Withers, Rhea Tumminkatti, Hasset T. Nurelegne, Alexander O. D. Gulka, Morris Wan, Jennifer M. Spangle
Somatic missense mutations in histone genes turn these essential proteins into oncohistones, which can drive oncogenesis. Understanding how missense mutations alter histone function is challenging in mammals as mutations occur in a single histone gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf35aea34fa1b5e61d7c9d904d0a78d3
https://doi.org/10.1101/2021.10.02.462853
https://doi.org/10.1101/2021.10.02.462853
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5d64bfa72e5212a1b375190661795c4
https://pubmed.ncbi.nlm.nih.gov/34162742
https://pubmed.ncbi.nlm.nih.gov/34162742
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