Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Remington E. Hoerr"'
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Telomeres, repetitive sequences located at the ends of most eukaryotic chromosomes, provide a mechanism to replenish terminal sequences lost during DNA replication, limit nucleolytic resection, and protect chromosome ends from engaging in double-stra
Externí odkaz:
https://doaj.org/article/47979d91ac1d4a27a5c3d66485362ae5
Autor:
Katrina Ngo, Tristen H. Gittens, David I. Gonzalez, E. Anne Hatmaker, Simcha Plotkin, Mason Engle, Geofrey A. Friedman, Melissa Goldin, Remington E. Hoerr, Brandt F. Eichman, Antonis Rokas, Mary Lauren Benton, Katherine L. Friedman
Publikováno v:
bioRxiv
Telomere healing occurs when telomerase, normally restricted to chromosome ends, acts upon a double-strand break to create a new, functional telomere. De novo telomere addition on the centromere-proximal side of a break truncates the chromosome but,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2410b9705d93038baebc442a13d64636
https://doi.org/10.1101/2023.03.20.533556
https://doi.org/10.1101/2023.03.20.533556
Autor:
Remington E Hoerr, Alex Eng, Celia Payen, Sara C Di Rienzi, M K Raghuraman, Maitreya J Dunham, Bonita J Brewer, Katherine L Friedman
Publikováno v:
GENETICS. 224
Evolution is driven by the accumulation of competing mutations that influence survival. A broad form of genetic variation is the amplification or deletion of DNA (≥50 bp) referred to as copy number variation (CNV). In humans, CNV may be inconsequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88f18188ce73e54d05eb860a33ba2ae1
https://doi.org/10.1093/genetics/iyad010
https://doi.org/10.1093/genetics/iyad010
Autor:
Remington E. Hoerr, Alex Eng, Celia Payen, Sara C. Di Rienzi, M. K. Raghuraman, Maitreya J. Dunham, Bonita J. Brewer, Katherine L. Friedman
Evolution is driven by the accumulation of competing mutations that influence survival. A broad form of genetic variation is the amplification or deletion of DNA (≥50 bp) referred to as copy number variation. In humans, copy number variation may be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f01d7894fa01806a081c5bc2420639c
https://doi.org/10.1101/2022.06.12.495855
https://doi.org/10.1101/2022.06.12.495855
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Telomeres, repetitive sequences located at the ends of most eukaryotic chromosomes, provide a mechanism to replenish terminal sequences lost during DNA replication, limit nucleolytic resection, and protect chromosome ends from engaging in double-stra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74f77d5bde177e3a5abcf21169c87652
https://pubmed.ncbi.nlm.nih.gov/33816507
https://pubmed.ncbi.nlm.nih.gov/33816507