selected publications
- Activation of RhoC by regulatory ubiquitination is mediated by LNX1 and suppressed by LIS1. Scientific reports. 2022 Academic Article GET IT
-
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.
Nature genetics.
2019
Academic Article
GET IT
Times cited: 24 -
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.
Nature genetics.
2014
Academic Article
GET IT
Times cited: 110 -
LRP6 exerts non-canonical effects on Wnt signaling during neural tube closure.
Human molecular genetics.
2013
Academic Article
GET IT
Times cited: 35 -
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome.
Nature genetics.
2012
Academic Article
GET IT
Times cited: 219 -
Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility.
Nature neuroscience.
2005
Academic Article
GET IT
Times cited: 130 -
Disregulated RhoGTPases and actin cytoskeleton contribute to the migration defect in Lis1-deficient neurons.
The Journal of neuroscience : the official journal of the Society for Neuroscience.
2003
Academic Article
GET IT
Times cited: 105 -
[Learning by mice of Y-maze using drinking reinforcement and aversive olfactory stimulus (beneficial effect of ginsenosides)].
Biulleten' eksperimental'noi biologii i meditsiny.
1996
Academic Article
GET IT
Times cited: 3 - [An aversive olfactory signal during the Y-maze learning of mice selected for greater or lesser brain weight]. Zhurnal vysshei nervnoi deiatelnosti imeni I P Pavlova. 1996 Academic Article GET IT