Search Results - Shawn Singh
- Showing 1 - 3 results of 3
-
1
-
2
-
3
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome by Ghayda Mirzaa, David Parry, Andrew E. Fry, Kristin A. Giamanco, Jeremy Schwartzentruber, Megan R. Vanstone, Clare V. Logan, Nicola Roberts, Colin A. Johnson, Shawn Singh, Stanislav S. Kholmanskikh, Carissa Adams, Rebecca D. Hodge, Robert F. Hevner, David T. Bonthron, Kees P. J. Braun, Laurence Faivre, Jean‐Baptiste Rivière, Judith St‐Onge, Karen W. Gripp, Grazia M.S. Mancini, Ki Pang, Elizabeth Sweeney, Hilde Van Esch, Nienke E. Verbeek, Dagmar Wieczorek, Michelle Steinraths, Jacek Majewski, Kym M. Boycott, Daniela T. Pilz, M. Elizabeth Ross, William B. Dobyns, Eamonn Sheridan
Published 2014Artigo
Search Tools:
Related Subjects
Biology
Signal transduction
AKT1
AKT3
Cancer research
Cell biology
Cell cycle
Chemistry
Closure (psychology)
Composite material
Computer science
Cyclin D1
Cyclin D2
Embryo
Epilepsy
GSK-3
Gene
Genetics
LRP6
Law
Materials science
Megalencephaly
Molecular biology
Neural tube
Neuroscience
PI3K/AKT/mTOR pathway
PTEN
Phosphorylation
Political science
Polymicrogyria