Zobrazeno 1 - 7
of 7
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
Autor:
Reyes-Serratos, Eduardo1,2 (AUTHOR), Ramielle L. Santos, Joy1,2 (AUTHOR), Puttagunta, Lakshmi1,3 (AUTHOR), Lewis, Stephen J.4 (AUTHOR), Watanabe, Mechiko4,5 (AUTHOR), Gonshor, Aron6 (AUTHOR), Buck, Robert6,7 (AUTHOR), Befus, A. Dean1,2 (AUTHOR) marcelo@ualberta.ca, Marcet-Palacios, Marcelo1,8 (AUTHOR) marcelo@ualberta.ca
Publikováno v:
PLoS ONE. 5/16/2024, Vol. 19 Issue 5, p1-22. 22p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
St. Laurent, Louis C
Thesis (Ph. D.)--Joint Program in Physical Oceanography (Massachusetts Institute of Technology, Dept. of Earth, Atmospheric, and Planetary Sciences; and the Woods Hole Oceanographic Institution), 1999.
Includes bibliographical references (leaves
Includes bibliographical references (leaves
Externí odkaz:
http://hdl.handle.net/1721.1/69185
L’anémie de Fanconi (FA) est une maladie congénitale rare résultant d’une mutation sur chaque allèle parental d’un gène FANC. Nous avons récemment identifié un variant d'épissage de FANCL contenant une exclusion de l'exon 4. Une analyse
Externí odkaz:
http://www.theses.ulaval.ca/2013/30232/30232.pdf