Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Cas9 genome editing"'
Publikováno v:
Molecular Autism, Vol 14, Iss 1, Pp 1-20 (2023)
Abstract Background Disruptions of SETBP1 (SET binding protein 1) on 18q12.3 by heterozygous gene deletion or loss-of-function variants cause SETBP1 disorder. Clinical features are frequently associated with moderate to severe intellectual disability
Externí odkaz:
https://doaj.org/article/9f18ceb82edc4d70ad9e05fbb7316ea1
Autor:
Abdulrezzak Memon
Publikováno v:
Turkish Journal of Agriculture: Food Science and Technology, Vol 9, Iss sp, Pp 2396-2400 (2021)
Recently, most genomic research has focused on genome editing methods to develop new technologies that could be easy, reliable, and feasible to edit plant genomes for highly productive agriculture. Genome editing is based on alternating a specific ta
Externí odkaz:
https://doaj.org/article/61b5e5c3e55245f0931cd0a4d4be1cb4
Publikováno v:
BMC Biotechnology, Vol 20, Iss 1, Pp 1-16 (2020)
Abstract Background Precise genetic modifications are preferred products of CRISPR-Cas9 mediated gene editing in mammalian cells but require the repair of induced double-strand breaks (DSB) through homology directed repair (HDR). Since HDR competes w
Externí odkaz:
https://doaj.org/article/494ce4496ccd4d98802430c0072600d6
Akademický článek
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Autor:
Jun Song, Guoshun Wang, Mark J. Hoenerhoff, Jinxue Ruan, Dongshan Yang, Jifeng Zhang, Jibing Yang, Patrick A. Lester, Robert Sigler, Michael Bradley, Samantha Eckley, Kelsey Cornelius, Kong Chen, Jay K. Kolls, Li Peng, Liang Ma, Yuqing Eugene Chen, Fei Sun, Jie Xu
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Using the CRISPR/Cas9 gene-editing technology, we recently produced a number of rabbits with mutations in immune function genes, including FOXN1, PRKDC, RAG1, RAG2, and IL2RG. Seven founder knockout rabbits (F0) and three male IL2RG null (−/y) F1 a
Externí odkaz:
https://doaj.org/article/007a244c6e3342348149e1e4967b1f19
Autor:
Abdulrezzak MEMON
Publikováno v:
Turkish Journal of Agriculture: Food Science and Technology, Vol 9, Iss sp, Pp 2396-2400 (2022)
Recently, most genomic research has focused on genome editing methods to develop new technologies that could be easy, reliable, and feasible to edit plant genomes for highly productive agriculture. Genome editing is based on alternating a specific ta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c375f043cf42218bc499db6316d7489e
http://www.agrifoodscience.com/index.php/TURJAF/article/view/4810
http://www.agrifoodscience.com/index.php/TURJAF/article/view/4810
Publikováno v:
BMC Biotechnology, Vol 20, Iss 1, Pp 1-16 (2020)
BMC Biotechnology
BMC Biotechnology
Background Precise genetic modifications are preferred products of CRISPR-Cas9 mediated gene editing in mammalian cells but require the repair of induced double-strand breaks (DSB) through homology directed repair (HDR). Since HDR competes with the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b598c3411360c6f84d17515eb436af1e
http://link.springer.com/article/10.1186/s12896-020-00650-x
http://link.springer.com/article/10.1186/s12896-020-00650-x
Autor:
Mingai Li, Martina Leso, Matteo Buti, Erika Bellini, Daniela Bertoldi, Alessandro Saba, Roberto Larcher, Luigi Sanità di Toppi, Claudio Varotto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e5ce8ec180cd2afaba1cfc6cdbccd1
http://hdl.handle.net/10449/76601
http://hdl.handle.net/10449/76601
Autor:
Matthias Rath, Konrad Schwefel, Matteo Malinverno, Dariush Skowronek, Alexandra Leopoldi, Robin A. Pilz, Doreen Biedenweg, Sander Bekeschus, Josef M. Penninger, Elisabetta Dejana, Ute Felbor
Cerebral cavernous malformations (CCM) are low-flow vascular lesions prone to cause severe hemorrhage-associated neurological complications. Pathogenic germline variants in CCM1, CCM2, or CCM3 can be identified in nearly 100% of CCM patients with a p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2e064c949ef46b13d12e9be577f5dae
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-477777
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-477777
Akademický článek
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