Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Brianne B. Rogers"'
Autor:
Susan M. Hiatt, James M.J. Lawlor, Lori H. Handley, Ryne C. Ramaker, Brianne B. Rogers, E. Christopher Partridge, Lori Beth Boston, Melissa Williams, Christopher B. Plott, Jerry Jenkins, David E. Gray, James M. Holt, Kevin M. Bowling, E. Martina Bebin, Jane Grimwood, Jeremy Schmutz, Gregory M. Cooper
Publikováno v:
HGG Advances, Vol 2, Iss 2, Pp 100023- (2021)
Summary: Exome and genome sequencing have proven to be effective tools for the diagnosis of neurodevelopmental disorders (NDDs), but large fractions of NDDs cannot be attributed to currently detectable genetic variation. This is likely, at least in p
Externí odkaz:
https://doaj.org/article/9e89b02fe99e4ca599239301f8118f70
Autor:
Brianne B. Rogers, Ashlyn G. Anderson, Shelby N. Lauzon, M. Natalie Davis, Rebecca M. Hauser, Sydney C. Roberts, Ivan Rodriguez-Nunez, Katie Trausch-Lowther, Erin A. Barinaga, Jared W. Taylor, Mark Mackiewicz, Brian S. Roberts, Sara J. Cooper, Lindsay F. Rizzardi, Richard M. Myers, J. Nicholas Cochran
BackgroundTauopathies are a group of neurodegenerative diseases driven by abnormal aggregates of tau, a microtubule associated protein encoded by theMAPTgene.MAPTexpression is absent in neural progenitor cells (NPCs) and increases during differentiat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b669916991844fab28b170d29302d08c
https://doi.org/10.1101/2023.03.07.531520
https://doi.org/10.1101/2023.03.07.531520
Autor:
Brianne B. Rogers, Shelby N. Lauzon, M. Natalie Davis, Ashlyn G Anderson, Lindsay F. Rizzardi, Sara J. Cooper, Richard M. Myers, J. Nicholas Cochran
Publikováno v:
Alzheimer's & Dementia. 18
Autor:
Ashlyn G. Anderson, Brianne B. Rogers, Jacob M. Loupe, Ivan Rodriguez-Nunez, Sydney C. Roberts, Lauren M. White, J. Nicholas Brazell, William E. Bunney, Blynn G. Bunney, Stanley J. Watson, J. Nicholas Cochran, Richard M. Myers, Lindsay F. Rizzardi
Publikováno v:
Cell Genomics. 3:100263
Autor:
Brianne B. Rogers, Shelby N. Lauzon, M. Natalie Davis, Lindsay F. Rizzardi, Sara J. Cooper, Richard M. Myers, J. Nicholas Cochran
Publikováno v:
Alzheimer's & Dementia. 17
Autor:
James M.J. Lawlor, Melissa Williams, Christopher Plott, Jane Grimwood, Martina Bebin, Jerry Jenkins, Lori H. Handley, Jeremy Schmutz, Lori Beth Boston, Brianne B. Rogers, Kevin M. Bowling, E. Christopher Partridge, Susan M. Hiatt, David Gray, James Holt, Gregory M. Cooper, Ryne C. Ramaker
Publikováno v:
HGG advances
HGG Advances, Vol 2, Iss 2, Pp 100023-(2021)
HGG Advances, Vol 2, Iss 2, Pp 100023-(2021)
Summary: Exome and genome sequencing have proven to be effective tools for the diagnosis of neurodevelopmental disorders (NDDs), but large fractions of NDDs cannot be attributed to currently detectable genetic variation. This is likely, at least in p
Autor:
Jeremy Schmutz, Ryne C. Ramaker, Brianne B. Rogers, Jerry Jenkins, Greg M. Cooper, James M.J. Lawlor, Williams M, Christopher Plott, Jane Grimwood, E. M. Bebin, Kevin M. Bowling, Lori H. Handley, Boston Lb, David E. Gray, James Holt, Partridge Ec, Susan M. Hiatt
PurposeExome and genome sequencing have proven to be effective tools for the diagnosis of neurodevelopmental disorders (NDDs), but large fractions of NDDs cannot be attributed to currently detectable genetic variation. This is likely, at least in par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::697abb2f25c2aef1f37908686a633e8e
https://doi.org/10.1101/2020.07.02.185447
https://doi.org/10.1101/2020.07.02.185447