K. Patterson

MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats

D. Mulkey, K. Patterson, V. Hawkins, 2016, Human molecular genetics.

Shared microbial community changes in female rats and humans with Rett syndrome

Laura G. Dubois, Casey D. Morrow, Susan Campbell, 2019 .

MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats

D. Mulkey, K. Patterson, V. Hawkins, 2016, Human molecular genetics.

The role of glial-specific Kir4.1 in normal and pathological states of the CNS

Sinifunanya E Nwaobi, K. Patterson, M. Olsen, 2016, Acta Neuropathologica.

Kir5.1‐dependent CO2/H+‐sensitive currents contribute to astrocyte heterogeneity across brain regions

J. Hablitz, A. Staruschenko, D. Mulkey, 2020, Glia.

Glial Dysfunction in MeCP2 Deficiency Models: Implications for Rett Syndrome

K. Patterson, M. Olsen, Raymundo Hernandez, 2019, International journal of molecular sciences.