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pro vyhledávání: '"Christopher St. Laurent"'
Autor:
Hansol Park, Eiman Osman, Christopher Cromwell, Christopher St. Laurent, Yuning Liu, Elena Kitova, John Klassen, Basil Hubbard, Matthew Macauley, Julianne Gibbs
Gene editing systems such as CRISPR/Cas9 readily enable individual gene phenotypes to be studied through loss-of-function. However, in certain instances, gene compensation can obfuscate the results of these studies, necessitating the editing of multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7085ca2b150ec3c213d36b52a14d27fc
https://doi.org/10.26434/chemrxiv-2021-7pdz9
https://doi.org/10.26434/chemrxiv-2021-7pdz9
Autor:
Yuning Liu, Basil P. Hubbard, Elena N. Kitova, John S. Klassen, Hansol Park, Christopher St. Laurent, Christopher R Cromwell, Matthew S. Macauley, Julianne M. Gibbs, Eiman A. Osman
Gene editing systems such as CRISPR/Cas9 readily enable individual gene phenotypes to be studied through loss-of-function. However, in certain instances, gene compensation can obfuscate the results of these studies, necessitating the editing of multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4750c23f1c637a7b36541f5ba6e2a5c4
https://doi.org/10.33774/chemrxiv-2021-7pdz9
https://doi.org/10.33774/chemrxiv-2021-7pdz9
Autor:
Francine Durocher, Yvan Labrie, Christopher St-Laurent Pedneault, Frédéric Guénard, Geneviève Ouellette, Jacques Simard
Publikováno v:
Genetic testing and molecular biomarkers. 14(4)
Inactivating mutations of the CHEK2 and STK11 genes are responsible for Li-Fraumeni and Peutz-Jeghers syndrome, respectively, both autosomal dominant syndromes associated with an increased risk of breast cancer. The PALB2/FANCN gene encodes a nuclear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::310475921cae48fb1979c9d04a392cf0
https://pubmed.ncbi.nlm.nih.gov/20722467
https://pubmed.ncbi.nlm.nih.gov/20722467
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