Zobrazeno 1 - 10
of 906
pro vyhledávání: '"J. Waite"'
Autor:
Christopher T. Esapa, R. A. Jeffrey McIlhinney, Adrian J. Waite, Matthew A. Benson, Jasmin Mirzayan, Henriett Piko, Ágnes Herczegfalvi, Rita Horvath, Veronika Karcagi, Maggie C. Walter, Hanns Lochmüller, Pierre J. Rizkallah, Qi L. Lu, Derek J. Blake
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Fukutin-related protein (FKRP, MIM ID 606596) variants cause a range of muscular dystrophies associated with hypo-glycosylation of the matrix receptor, α-dystroglycan. These disorders are almost exclusively caused by homozygous or compound heterozyg
Externí odkaz:
https://doaj.org/article/35da4e2141714c0fa0e8671065cea821
Autor:
Christopher J. Waite, Anya Lindström Battle, Mark H. Bennett, Matthew R. Carey, Chun K. Hong, Ioly Kotta-Loizou, Martin Buck, Jörg Schumacher
Publikováno v:
Frontiers in Microbiology, Vol 12 (2021)
Free-living nitrogen-fixing bacteria can improve growth yields of some non-leguminous plants and, if enhanced through bioengineering approaches, have the potential to address major nutrient imbalances in global crop production by supplementing inorga
Externí odkaz:
https://doaj.org/article/6d56a453d1084c27a0e5026829a6be78
Autor:
David E. Paschon, Stephanie Lussier, Tenzin Wangzor, Danny F. Xia, Patrick W. Li, Sarah J. Hinkley, Nicholas A. Scarlott, Stephen C. Lam, Adam J. Waite, Lynn N. Truong, Nimisha Gandhi, Bhakti N. Kadam, Deepak P. Patil, David A. Shivak, Gary K. Lee, Michael C. Holmes, Lei Zhang, Jeffrey C. Miller, Edward J. Rebar
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
Genome editing often requires cleavage within a narrow sequence window. Here the authors develop an expanded set of zinc finger nuclease architectures that increase the available configurations by a factor of 64 and can target almost every base at lo
Externí odkaz:
https://doaj.org/article/52399a6682884a7196ea64923e436811
Autor:
Adaku C. Ume, Tara Y. Wenegieme, Jennae N. Shelby, Chiagozie D. B. Paul-Onyia, Aston M. J. Waite, John K. Kamau, Danielle N. Adams, Keiichiro Susuki, Eric S. Bennett, Hongmei Ren, Clintoria R. Williams
Publikováno v:
American Journal of Physiology-Renal Physiology. 324:F433-F445
Renal fibrosis, a detrimental feature of irreversible kidney damage, remains a sinister consequence of long-term calcineurin inhibitor (CNI) immunosuppressive therapy. Our study not only incorporates renal fibroblasts into the growing list of cell ty
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102018- (2020)
FOXG1 syndrome is a neurodevelopmental disorder caused by mutations in the FOXG1 gene. Here, an induced pluripotent stem cell (iPSC) line was generated from human dermal fibroblasts of an individual with the c.490dupG (p.Glu154fs) mutation in the FOX
Externí odkaz:
https://doaj.org/article/09f7faec576842bb9733a2d899cb4e50
Autor:
Matthew A. Benson, Caroline L. Tinsley, Adrian J. Waite, Francesca A. Carlisle, Steve M. M. Sweet, Elisabeth Ehler, Christopher H. George, F. Anthony Lai, Enca Martin-Rendon, Derek J. Blake
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract The Cardiomyopathy–associated gene 5 (Cmya5) encodes myospryn, a large tripartite motif (TRIM)-related protein found predominantly in cardiac and skeletal muscle. Cmya5 is an expression biomarker for a number of diseases affecting striated
Externí odkaz:
https://doaj.org/article/15612c84e60c4397ba603b292142ca3f
Autor:
Jianfeng Xiao, Satya R. Vemula, Yi Xue, Mohammad M. Khan, Francesca A. Carlisle, Adrian J. Waite, Derek J. Blake, Ioannis Dragatsis, Yu Zhao, Mark S. LeDoux
Publikováno v:
Neurobiology of Disease, Vol 98, Iss , Pp 52-65 (2017)
Loss-of-function mutations in SGCE, which encodes ε-sarcoglycan (ε-SG), cause myoclonus-dystonia syndrome (OMIM159900, DYT11). A “major” ε-SG protein derived from CCDS5637.1 (NM_003919.2) and a “brain-specific” protein, that includes seque
Externí odkaz:
https://doaj.org/article/4a2699bf291c44c08161fe58f410f8fd
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