Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ryan M, Marks"'
Autor:
Allen C.T. Teng, Marjan Tavassoli, Suja Shrestha, Ryan M. Marks, Meghan J. McFadden, Sonia L. Evagelou, Kyle Lindsay, Ava Vandenbelt, Wenping Li, Evgueni Ivakine, Ronald Cohn, J. Paul Santerre, Anthony O. Gramolini
Publikováno v:
STAR Protocols, Vol 4, Iss 1, Pp 101933- (2023)
Summary: Here, we describe a protocol for purifying functional clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (Cas9) from Staphylococcus aureus within 24 h and over 90% purity. SaCas9 purification begins with
Externí odkaz:
https://doaj.org/article/d1573157b4e54e4c84f54302f66cee69
Autor:
Harshavardhan Lingegowda, Jessica E. Miller, Ryan M. Marks, Lindsey K. Symons, Taylor Alward, Alan E. Lomax, Madhuri Koti, Chandrakant Tayade
Publikováno v:
Frontiers in Reproductive Health, Vol 3 (2021)
Endometriosis (EM) is characterized by the growth of endometrium-like tissue outside the uterus, leading to chronic inflammation and pelvic pain. Lesion proliferation, vascularization, and associated inflammation are the hallmark features of EM lesio
Externí odkaz:
https://doaj.org/article/14b223a4f302427d96f8b58163612051
Autor:
Sina Fatehi, Ryan M. Marks, Matthew J. Rok, Lucie Perillat, Evgueni A. Ivakine, Ronald D. Cohn
Publikováno v:
Human Gene Therapy. 34:388-403
Autor:
Jessica E. Miller, Soo Hyun Ahn, Ryan M. Marks, Stephany P. Monsanto, Asgerally T. Fazleabas, Madhuri Koti, Chandrakant Tayade
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Endometriosis is a debilitating gynecological disease characterized by the extrauterine presence of endometrial-like tissues located on the peritoneal membrane and organs of the pelvic cavity. Notably, dysfunctional immune activation in women with en
Externí odkaz:
https://doaj.org/article/d74af855d4a6448ea6e0617381023612
Publikováno v:
Immunology of Endometriosis ISBN: 9780128206614
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::174feb3fa7db6ae6107731ff4af51e14
https://doi.org/10.1016/b978-0-12-820661-4.00002-9
https://doi.org/10.1016/b978-0-12-820661-4.00002-9
Autor:
M.S. Abrão, Jodie Avery, Fabio Barra, Charles Chapron, Giulio Evangelisti, Simone Ferrero, Akira Fujishita, Linda C. Giudice, Erin Greaves, Sun-Wei Guo, Tasuku Harada, Ying He, Takehiro Hiraoka, Mary Louise Hull, Sze Wan Hung, Gentaro Izumi, Miaomiao Ji, Xue Jiao, Yoshimasa Kamei, Khaleque N. Khan, Michio Kitajima, Jo Kitawaki, Hiroshi Kobayashi, Kaori Koga, Hiroaki Komatsu, Mathew Leonardi, Tin-Chiu Li, Wan-Ning Li, Harshavardhan Lingegowda, Louis Marcellin, Ryan M. Marks, Alison McCallion, Taisuke Mori, Anushka Nair, Yosuke Ono, Yutaka Osuga, Kavita Panir, L.G.C. Riccio, Pietro Santulli, Carolina Scala, Masashi Takamura, Yukiko Tanaka, Fuminori Taniguchi, Chandrakant Tayade, Shaw-Jenq Tsai, Júlia Vallvé-Juanico, Chi-Chiu Wang, Guoyun Wang, Meng Hsing Wu, Hui Xu, Osamu Yoshino, Tao Zhang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21e1f3560488c7a1f3318d7290b89a90
https://doi.org/10.1016/b978-0-12-820661-4.01002-5
https://doi.org/10.1016/b978-0-12-820661-4.01002-5
Autor:
Dwi U, Kemaladewi, Prabhpreet S, Bassi, Steven, Erwood, Dhekra, Al-Basha, Kinga I, Gawlik, Kyle, Lindsay, Elzbieta, Hyatt, Rebekah, Kember, Kara M, Place, Ryan M, Marks, Madeleine, Durbeej, Steven A, Prescott, Evgueni A, Ivakine, Ronald D, Cohn
Publikováno v:
Nature. 572(7767)
Neuromuscular disorders are often caused by heterogeneous mutations in large, structurally complex genes. Targeting compensatory modifier genes could be beneficial to improve disease phenotypes. Here we report a mutation-independent strategy to upreg