Zobrazeno 1 - 10
of 21
pro vyhledávání: '"H. Valley"'
Autor:
Gregory A. Newby, Luke H. Rhym, Hermann Bihler, Zhiping Weng, Martin Mense, Tingting Jiang, Wen Xue, Xiao-Ou Zhang, Y. Cheng, Jordana M. Henderson, H. Valley, Yueying Cao, Anton P. McCaffrey, Daniel G. Anderson, David R. Liu, Qin Wang, Kevin Coote
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Nature Communications
Nature Communications
CRISPR-Cas9-associated base editing is a promising tool to correct pathogenic single nucleotide mutations in research or therapeutic settings. Efficient base editing requires cellular exposure to levels of base editors that can be difficult to attain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb61cea1d36ee5309fa0957875fb1f9f
https://doaj.org/article/063c642bedca45fb8d0878850da6e48f
https://doaj.org/article/063c642bedca45fb8d0878850da6e48f
Autor:
K. Bukis, Y. Cheng, M. Armstrong, J. Conte, K. Coote, N. Allaire, A. Sivachenko, M. Mense, C. Cotton, H. Valley
Publikováno v:
Journal of Cystic Fibrosis. 21:S349
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91905097c1b7a0249be812bde84b8f29
https://doi.org/10.1016/s1569-1993(22)01324-8
https://doi.org/10.1016/s1569-1993(22)01324-8
Autor:
N. Allaire, J. Yoon, M. Armstrong, H. Valley, C. Macadino, A. Sivachenko, J. Conte, B. Tabak, H. Bihler, Y. Cheng, K. Coote, C. Cotton, M. Mense
Publikováno v:
Journal of Cystic Fibrosis. 21:S363
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07825d08c2b62feeb356179714b6018c
https://doi.org/10.1016/s1569-1993(22)01353-4
https://doi.org/10.1016/s1569-1993(22)01353-4
Autor:
F. Liang, H. Shang, Y. Cheng, L. Wang, S. Cantu, J. Shepard, A. Bell, H. Valley, K. Coote, H. Bihler, M. Mense
Publikováno v:
Journal of Cystic Fibrosis. 21:S340
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6441b2394539fad3d209e40dc12b4e96
https://doi.org/10.1016/s1569-1993(22)01304-2
https://doi.org/10.1016/s1569-1993(22)01304-2
Autor:
Martin Mense, Calvin U. Cotton, J. Harrington, N. Allaire, Andrey Sivachenko, J. Conte, B. Tabak, Hermann Bihler, E. Wilson, A. LaPan, H. Valley
Publikováno v:
Journal of Cystic Fibrosis. 20:S302-S303
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::210fee921ea9c8e606fc65ccadb1e64c
https://doi.org/10.1016/s1569-1993(21)02060-9
https://doi.org/10.1016/s1569-1993(21)02060-9
Autor:
Feng Liang, Nikole J Jordan, H. Valley, L. Wang, Hermann Bihler, H. Shang, K. Coote, A. Bell, Y. Cheng, S. Cantu, Martin Mense
Publikováno v:
Journal of Cystic Fibrosis. 20:S280-S281
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff3979898321a68d3c085eab2a63bb11
https://doi.org/10.1016/s1569-1993(21)02014-2
https://doi.org/10.1016/s1569-1993(21)02014-2
Autor:
R. Seymour, Junjie Lu, K. Bukis, J. Harrington, M. Simpkinson, A. Bell, K. Coote, Andrey Sivachenko, Finn Hawkins, B. Tabak, H. Valley, Martin Mense, A. Stuffer, John Mahoney, Calvin U. Cotton
Publikováno v:
Journal of Cystic Fibrosis. 20:S320
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10883513d4cad9c97d6f802e6500a6b1
https://doi.org/10.1016/s1569-1993(21)02098-1
https://doi.org/10.1016/s1569-1993(21)02098-1
Autor:
E. Wilson, Calvin U. Cotton, R. Seymour, A. Bell, Martin Mense, Y. Cheng, H. Valley, K. Coote, K. Bukis, Hermann Bihler, N. Allaire, J. Conte, Andrey Sivachenko
Publikováno v:
Journal of Cystic Fibrosis. 20:S319
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb508f726c66c3b2864475c68d9cd33a
https://doi.org/10.1016/s1569-1993(21)02095-6
https://doi.org/10.1016/s1569-1993(21)02095-6
Autor:
H. Valley, Martin Mense, Hermann Bihler, Eric Wong, Melissa M. Keenan, Jerome Mahiou, Feng Liang, Nikole J Jordan, Shuling Guo, Y. Cheng, Brett P. Monia, Lulu Huang
Publikováno v:
American journal of respiratory cell and molecular biology. 61(3)
The recessive genetic disease cystic fibrosis (CF) is caused by loss-of-function mutations in the CFTR (CF transmembrane conductance regulator) gene. Approximately 10% of patients with CF have at least one allele with a nonsense mutation in CFTR. Non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61e5a79ee55596178cb396a4c8b2c548
https://pubmed.ncbi.nlm.nih.gov/30836009
https://pubmed.ncbi.nlm.nih.gov/30836009
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