Kenneth Campbell

9PUBLICATIONS
8CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Central nervous systemNeurology and neuromuscular diseasesImmunogenetics (incl. genetic immunology)
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Publications (9)

|Jan 30, 2025
Modelling a pathological GSX2 variant that selectively alters DNA binding reveals hypomorphic mouse brain defects.

Laura Tweedie, Matthew R Riccetti, Brittany Cain

|Sep 20, 2022
Conserved and Distinct Functions of the Autism-Related Chromatin Remodeler CHD8 in Embryonic and Adult Forebrain Neurogenesis.

Chen Dong, Chuntao Zhao, Xiang Chen

|Mar 11, 2022
Formation of the Mouse Internal Capsule and Cerebral Peduncle: A Pioneering Role for Striatonigral Axons as Revealed in Isl1 Conditional Mutants.

Jacqueline M Ehrman, Paloma Merchan-Sala, Lisa A Ehrman

|Jan 07, 2022
The Anti-Inflammatory Agent Bindarit Attenuates the Impairment of Neural Development through Suppression of Microglial Activation in a Neonatal Hydrocephalus Mouse Model.

Eri Iwasawa, Farrah N Brown, Crystal Shula

|Mar 04, 2020
Physical interactions between Gsx2 and Ascl1 balance progenitor expansion versus neurogenesis in the mouse lateral ganglionic eminence.

Kaushik Roychoudhury, Joseph Salomone, Shenyue Qin

|Aug 26, 2018
DMRT5, DMRT3, and EMX2 Cooperatively Repress Gsx2 at the Pallium-Subpallium Boundary to Maintain Cortical Identity in Dorsal Telencephalic Progenitors.

Elodie Desmaris, Marc Keruzore, Amandine Saulnier

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