Zobrazeno 1 - 10
of 186
pro vyhledávání: '"Kevin Ban"'
Autor:
PR Newswire
Publikováno v:
PR Newswire US. 06/10/2024.
Autor:
PR Newswire
Publikováno v:
PR Newswire US. 10/17/2023.
Autor:
Jessica E. MacLean, Jaime N. Wertman, Sergey V. Prykhozhij, Emily Chedrawe, Stewart Langley, Shelby L. Steele, Kevin Ban, Kim Blake, Jason N. Berman
Publikováno v:
Genes, Vol 14, Iss 5, p 1086 (2023)
CHARGE syndrome typically results from mutations in the gene encoding chromodomain helicase DNA-binding protein 7 (CHD7). CHD7 is involved in regulating neural crest development, which gives rise to tissues of the skull/face and the autonomic nervous
Externí odkaz:
https://doaj.org/article/7539def975c3466e8869d76f791114d6
Publikováno v:
Re:GEN Open, Vol 1, Iss 1, Pp 53-67 (2021)
Background: Knock-in of precise point mutations into protein-coding genes is among the most important applications of Clustered Regularly Interspaced Palindromic Repeats (CRISPR)/Cas9. Precise introduction of amino acid changes is crucial to interrog
Externí odkaz:
https://doaj.org/article/182893102dff4ee6bb624489a92450b8
Autor:
Sergey V. Prykhozhij, Lucia Caceres, Kevin Ban, Anna Cordeiro-Santanach, Kanneboyina Nagaraju, Eric P. Hoffman, Jason N. Berman
Publikováno v:
Genes, Vol 14, Iss 2, p 492 (2023)
Limb-Girdle Muscular Dystrophy Type R1 (LGMDR1; formerly LGMD2A), characterized by progressive hip and shoulder muscle weakness, is caused by mutations in CAPN3. In zebrafish, capn3b mediates Def-dependent degradation of p53 in the liver and intestin
Externí odkaz:
https://doaj.org/article/a7513d9d53ac44c086725e1d0d525d19
Autor:
Pifer, Rebecca
Publikováno v:
Healthcare Dive; 11/10/2023, p1-1, 1p
Publikováno v:
Healthcare Dive; 11/10/2023, p1-1, 1p
Autor:
Alejandro C. Arroliga, William H. Shrank, Brian Caveney, Benjamin Doga, Ian Tong, Sreekanth K. Chaguturu, Rhonda M. Medows, Steve Miller, Kevin Ban, J. Michael Seiden, Jay Wohlgemuth, Sean Muldoon
Publikováno v:
Population Health Management
Autor:
Christopher R. McMaster, Jason N. Berman, Lucia Caceres, Kevin Ban, Sergey V. Prykhozhij, Johane M Robitaille
Publikováno v:
Blood. 138:2071-2071
Defects in multiple cell signaling molecules lead to disruptions of vascular integrity given the need for fine-tuned regulation of the cell adhesion complexes. These genetic defects have been linked to the development of intracerebral hemorrhage (ICH
Autor:
Rutherford, Fiona (AUTHOR), Tozzi, John (AUTHOR)
Publikováno v:
Bloomberg.com. 11/10/2023, pN.PAG-N.PAG. 1p.