Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lindsey N. Guerin"'
Autor:
Xiang Ye, Lindsey N. Guerin, Ziche Chen, Suba Rajendren, William Dunker, Yang Zhao, Ruilin Zhang, Emily Hodges, John Karijolich
Publikováno v:
Cell Reports, Vol 43, Iss 3, Pp 113888- (2024)
Summary: Higher-order genome structure influences the transcriptional regulation of cellular genes through the juxtaposition of regulatory elements, such as enhancers, close to promoters of target genes. While enhancer activation has emerged as an im
Externí odkaz:
https://doaj.org/article/81686b9dcf8f42048fee6a344ff48f21
Autor:
Violeta Sánchez, Yaomin Xu, Douglas B Johnson, Emily Hodges, Margaret L Axelrod, Justin M Balko, Xiaopeng Sun, Brandie C Taylor, Catherine C Fahey, Jamaal L James, Lindsey N Guerin, Paula I Gonzalez-Ericsson, Melinda E Sanders
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 11, Iss 11 (2023)
Background Despite the remarkable success of immunotherapy in treating melanoma, understanding of the underlying mechanisms of resistance remains limited. Emerging evidence suggests that upregulation of tumor-specific major histocompatibility complex
Externí odkaz:
https://doaj.org/article/9daebf72a8f642c3941201c11f10699f
Publikováno v:
Nature Protocols. 16:5377-5397
The epigenome is multidimensional, with individual molecular components operating on different levels to control transcriptional output. Techniques that combine measurements of these features can reveal their precise correspondence in genomic space,
Autor:
Matthew T. Jenkins, Timothy J Scott, Lindsey N Guerin, Alana M Franceski, Yunli E Chu, Pawan Bhat, Chad R. Potts, Robert S. Welner, Emily Hodges, Brent Ferrell
Publikováno v:
Blood. 140:2883-2884
Autor:
Hiruy S. Meharena, Asaf Marco, Vishnu Dileep, Elana R. Lockshin, Grace Y. Akatsu, James Mullahoo, L. Ashley Watson, Tak Ko, Lindsey N. Guerin, Fatema Abdurrob, Shruthi Rengarajan, Malvina Papanastasiou, Jacob D. Jaffe, Li-Huei Tsai
Publikováno v:
Cell Stem Cell
Down syndrome (DS) is a genetic disorder driven by the triplication of chromosome 21 (T21) that is characterized by a wide-range of neurodevelopmental and physical disabilities. Transcriptomic analysis of tissue samples from individuals with DS has r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f3119ac0c9f90e9f1bf1a47524a9b8a
https://europepmc.org/articles/PMC8805993/
https://europepmc.org/articles/PMC8805993/