Detalhe da pesquisa
1.
Grey matter heterotopia subtypes show specific morpho-electric signatures and network dynamics.
Brain
; 147(3): 996-1010, 2024 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37724593
2.
Lis1 mutation prevents basal radial glia-like cell production in the mouse.
Hum Mol Genet
; 31(6): 942-957, 2022 03 21.
Artigo
Inglês
| MEDLINE | ID: mdl-34635911
3.
Visualising the cytoskeletal machinery in neuronal growth cones using cryo-electron tomography.
J Cell Sci
; 135(7)2022 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35383828
4.
Human cerebral organoids reveal progenitor pathology in EML1-linked cortical malformation.
EMBO Rep
; 23(5): e54027, 2022 05 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35289477
5.
RAB6 and dynein drive post-Golgi apical transport to prevent neuronal progenitor delamination.
EMBO Rep
; 23(10): e54605, 2022 10 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35979738
6.
A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture.
Neurobiol Dis
; 180: 106085, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36933672
7.
Genetics and mechanisms leading to human cortical malformations.
Semin Cell Dev Biol
; 76: 33-75, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-28951247
8.
Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development.
Hum Mol Genet
; 27(2): 224-238, 2018 01 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29077851
9.
EML1-associated brain overgrowth syndrome with ribbon-like heterotopia.
Am J Med Genet C Semin Med Genet
; 181(4): 627-637, 2019 12.
Artigo
Inglês
| MEDLINE | ID: mdl-31710781
10.
Early born neurons are abnormally positioned in the doublecortin knockout hippocampus.
Hum Mol Genet
; 26(1): 90-108, 2017 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28007902
11.
The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia.
J Anat
; 235(3): 637-650, 2019 09.
Artigo
Inglês
| MEDLINE | ID: mdl-31173351
12.
Cortical progenitor biology: key features mediating proliferation versus differentiation.
J Neurochem
; 146(5): 500-525, 2018 09.
Artigo
Inglês
| MEDLINE | ID: mdl-29570795
13.
Neuronal migration disorders: Focus on the cytoskeleton and epilepsy.
Neurobiol Dis
; 92(Pt A): 18-45, 2016 08.
Artigo
Inglês
| MEDLINE | ID: mdl-26299390
14.
Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown.
Hum Mol Genet
; 23(6): 1516-26, 2014 Mar 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24179174
15.
Rotatin' the phenotypes.
Brain
; 142(4): 834-838, 2019 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-30946475
16.
Long-term modifications of epileptogenesis and hippocampal rhythms after prolonged hyperthermic seizures in the mouse.
Neurobiol Dis
; 69: 156-68, 2014 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-24874545
17.
New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.
Brain
; 136(Pt 1): 223-44, 2013 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-23365099
18.
Fishing damage to cloud sponges may lead to losses in associated fish communities in Pacific Canada.
Mar Environ Res
; 197: 106448, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38518407
19.
Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway.
Hum Mol Genet
; 19(18): 3599-613, 2010 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-20603323
20.
Cellular anatomy, physiology and epileptiform activity in the CA3 region of Dcx knockout mice: a neuronal lamination defect and its consequences.
Eur J Neurosci
; 35(2): 244-56, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22250815