ReMAPping the microtubule landscape: How phosphorylation dictates the activities of microtubule‐associated proteins

A Ramkumar, BY Jong… - Developmental …, 2018 - Wiley Online Library
Classical microtubule‐associated proteins (MAPs) were originally identified based on their
co‐purification with microtubules assembled from mammalian brain lysate. They have since …

Lissencephaly and the molecular basis of neuronal migration

M Kato, WB Dobyns - Human molecular genetics, 2003 - academic.oup.com
Migration of post-mitotic neurons from the ventricular zone to the cortical plate during
embryogenesis comprises one of the most critical stages in brain development. Deficiency of …

Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration

T Tanaka, FF Serneo, C Higgins, MJ Gambello… - The Journal of cell …, 2004 - rupress.org
Humans with mutations in either DCX or LIS1 display nearly identical neuronal migration
defects, known as lissencephaly. To define subcellular mechanisms, we have combined in …

Distinct features of doublecortin as a marker of neuronal migration and its implications in cancer cell mobility

AA Ayanlaja, Y Xiong, Y Gao, GQ Ji, C Tang… - Frontiers in molecular …, 2017 - frontiersin.org
Neuronal migration is a critical process in the development of the nervous system. Defects in
the migration of the neurons are associated with diseases like lissencephaly, subcortical …

Genetics and mechanisms leading to human cortical malformations

DM Romero, N Bahi-Buisson, F Francis - Seminars in cell & developmental …, 2018 - Elsevier
Cerebral cortical development involves a complex series of highly regulated steps to
generate the laminated structure of the adult neocortex. Neuronal migration is a key part of …

Mechanism of microtubule stabilization by doublecortin

CA Moores, M Perderiset, F Francis, J Chelly… - Molecular cell, 2004 - cell.com
Neurons undertake an amazing journey from the center of the developing mammalian brain
to the outer layers of the cerebral cortex. Doublecortin, a component of the microtubule …

Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)

K Poirier, DA Keays, F Francis, Y Saillour… - Human …, 2007 - Wiley Online Library
We have recently reported a missense mutation in exon 4 of the tubulin alpha 1A (Tuba1a)
gene in a hyperactive N‐ethyl‐N‐nitrosourea (ENU) induced mouse mutant with abnormal …

The diverse genetic landscape of neurodevelopmental disorders

WF Hu, MH Chahrour, CA Walsh - Annual review of genomics …, 2014 - annualreviews.org
Advances in genetic tools and sequencing technology in the past few years have vastly
expanded our understanding of the genetics of neurodevelopmental disorders. Recent high …

[HTML][HTML] Cdk5 phosphorylation of doublecortin ser297 regulates its effect on neuronal migration

T Tanaka, FF Serneo, HC Tseng, AB Kulkarni, LH Tsai… - Neuron, 2004 - cell.com
Mutations in the doublecortin (DCX) gene in human or targeted disruption of the cdk5 gene
in mouse lead to similar cortical lamination defects in the developing brain. Here we show …

The centrosome in human genetic disease

JL Badano, TM Teslovich, N Katsanis - Nature Reviews Genetics, 2005 - nature.com
The centrosome is an indispensable component of the cell-cycle machinery of eukaryotic
cells, and the perturbation of core centrosomal or centrosome-associated proteins is linked …