JNK signaling: regulation and functions based on complex protein-protein partnerships

A Zeke, M Misheva, A Reményi… - … and Molecular Biology …, 2016 - Am Soc Microbiol
The c-Jun N-terminal kinases (JNKs), as members of the mitogen-activated protein kinase
(MAPK) family, mediate eukaryotic cell responses to a wide range of abiotic and biotic stress …

Growth and folding of the mammalian cerebral cortex: from molecules to malformations

T Sun, RF Hevner - Nature Reviews Neuroscience, 2014 - nature.com
The size and extent of folding of the mammalian cerebral cortex are important factors that
influence a species' cognitive abilities and sensorimotor skills. Studies in various animal …

The genetics of primary microcephaly

D Jayaraman, BI Bae, CA Walsh - Annual review of genomics …, 2018 - annualreviews.org
Primary microcephaly (MCPH, for “microcephaly primary hereditary”) is a disorder of brain
development that results in a head circumference more than 3 standard deviations below …

Small organelle, big responsibility: the role of centrosomes in development and disease

PL Chavali, M Pütz, F Gergely - … Transactions of the …, 2014 - royalsocietypublishing.org
The centrosome, a key microtubule organizing centre, is composed of centrioles, embedded
in a protein-rich matrix. Centrosomes control the internal spatial organization of somatic …

Microcephaly proteins Wdr62 and Aspm define a mother centriole complex regulating centriole biogenesis, apical complex, and cell fate

D Jayaraman, A Kodani, DM Gonzalez, JD Mancias… - Neuron, 2016 - cell.com
Mutations in several genes encoding centrosomal proteins dramatically decrease the size of
the human brain. We show that Aspm (abnormal spindle-like, microcephaly-associated) and …

Autosomal recessive primary microcephaly: not just a small brain

S Zaqout, AM Kaindl - Frontiers in Cell and Developmental Biology, 2022 - frontiersin.org
Microcephaly or reduced head circumference results from a multitude of abnormal
developmental processes affecting brain growth and/or leading to brain atrophy. Autosomal …

Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size

JF Chen, Y Zhang, J Wilde, KC Hansen, F Lai… - Nature …, 2014 - nature.com
Human genetic studies have established a link between a class of centrosome proteins and
microcephaly. Current studies of microcephaly focus on defective centrosome/spindle …

Proximity labeling reveals non-centrosomal microtubule-organizing center components required for microtubule growth and localization

AD Sanchez, TC Branon, LE Cote, A Papagiannakis… - Current Biology, 2021 - cell.com
Microtubules are polarized intracellular polymers that play key roles in the cell, including in
transport, polarity, and cell division. Across eukaryotic cell types, microtubules adopt diverse …

Molecular and cellular basis of autosomal recessive primary microcephaly

M Barbelanne, WY Tsang - BioMed research international, 2014 - Wiley Online Library
Autosomal recessive primary microcephaly (MCPH) is a rare hereditary
neurodevelopmental disorder characterized by a marked reduction in brain size and …

Kinetochore KMN network gene CASC5 mutated in primary microcephaly

A Genin, J Desir, N Lambert, M Biervliet… - Human molecular …, 2012 - academic.oup.com
Several genes expressed at the centrosome or spindle pole have been reported to underlie
autosomal recessive primary microcephaly (MCPH), a neurodevelopmental disorder …