Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Zachary Stephens"'
Autor:
Zachary Stephens, Jean-Pierre Kocher
Publikováno v:
BMC Bioinformatics, Vol 25, Iss 1, Pp 1-19 (2024)
Abstract Telomeres are regions of repetitive DNA at the ends of linear chromosomes which protect chromosome ends from degradation. Telomere lengths have been extensively studied in the context of aging and disease, though most studies use average tel
Externí odkaz:
https://doaj.org/article/e3ee243054fa492db1f5d93399580588
Autor:
Angela S. Cotera, Matthew J. Hankins, SOFIA Galactic Center Legacy Project, John Bally, Ashley T. Barnes, Cara D. Battersby, H. Perry Hatchfield, Terry L. Herter, Ryan M. Lau, Steven N. Longmore, Elisabeth A. C. Mills, Mark R. Morris, James T. Radomski, Janet P. Simpson, Zachary Stephens, Daniel L. Walker
Publikováno v:
The Astrophysical Journal, Vol 973, Iss 2, p 110 (2024)
The central regions of the Milky Way constitute a unique laboratory for a wide swath of astrophysical studies; consequently, the inner ∼400 pc have been the target of numerous large surveys at all accessible wavelengths. In this paper, we present a
Externí odkaz:
https://doaj.org/article/6f3538a8f9c0459f998d40ab47538675
Publikováno v:
Molecules, Vol 27, Iss 18, p 6124 (2022)
Similarities and differences of halogen and hydrogen bonding were explored via UV–Vis and 1H NMR measurements, X-ray crystallography and computational analysis of the associations of CHX3 (X=I, Br, Cl) with aromatic (tetramethyl-p-phenylenediamine)
Externí odkaz:
https://doaj.org/article/bc26dab6ce57498cbf0096a172bac07f
Autor:
Zachary Stephens, Dragana Milosevic, Benjamin Kipp, Stefan Grebe, Ravishankar K. Iyer, Jean-Pierre A. Kocher
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Long read sequencing technologies have the potential to accurately detect and phase variation in genomic regions that are difficult to fully characterize with conventional short read methods. These difficult to sequence regions include several clinic
Externí odkaz:
https://doaj.org/article/b11181a9f8864e89816d3eb364e98c24
Publikováno v:
BMC Bioinformatics, Vol 19, Iss S20, Pp 67-77 (2018)
Abstract Background With applications in cancer, drug metabolism, and disease etiology, understanding structural variation in the human genome is critical in advancing the thrusts of individualized medicine. However, structural variants (SVs) remain
Externí odkaz:
https://doaj.org/article/b32429e314074a258bfcb93fdbb3cf70
Autor:
Zachary Stephens, Daniel O'Brien, Mrunal Dehankar, Lewis R Roberts, Ravishankar K Iyer, Jean-Pierre Kocher
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0250915 (2021)
The integration of viruses into the human genome is known to be associated with tumorigenesis in many cancers, but the accurate detection of integration breakpoints from short read sequencing data is made difficult by human-viral homologies, viral ge
Externí odkaz:
https://doaj.org/article/be96bb101e274e2d9e876b69d9b85acf
Publikováno v:
Bioinformatics
Motivation Telomeres are the repetitive sequences found at the ends of eukaryotic chromosomes and are often thought of as a ‘biological clock,’ with their average length shortening during division in most cells. In addition to their association w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc5b3bb50c77c5215ec8783d56a807b5
https://europepmc.org/articles/PMC8963315/
https://europepmc.org/articles/PMC8963315/
Autor:
Zachary Stephens
Publikováno v:
The Quarterly Review of Biology. 92:79-80
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d31240300a9c5ae51268343181ec7e7
https://doi.org/10.1086/690842
https://doi.org/10.1086/690842