MicroRNAs: Not “Fine-Tuners” but Key Regulators of Neuronal Development and Function

by Davis, Gregory M., Haas, Matilda A., Pocock, Roger
Published 2015

Visualization and Genetic Manipulation of Dendrites and Spines in the Mouse Cerebral Cortex and Hippocampus using In utero Electroporation

by Pacary, Emilie, Haas, Matilda A., Wildner, Hendrik, Azzarelli, Roberta, Bell, Donald M., Abrous, Djoher Nora, Guillemot, François
Published 2012

Alterations to Dendritic Spine Morphology, but Not Dendrite Patterning, of Cortical Projection Neurons in Tc1 and Ts1Rhr Mouse Models of Down Syndrome

by Haas, Matilda A., Bell, Donald, Slender, Amy, Lana-Elola, Eva, Watson-Scales, Sheona, Fisher, Elizabeth M. C., Tybulewicz, Victor L. J., Guillemot, François
Published 2013

Bacurd2 is a novel interacting partner to Rnd2 which controls radial migration within the developing mammalian cerebral cortex

by Gladwyn-Ng, Ivan Enghian, Li, Shan Shan, Qu, Zhengdong, Davis, John Michael, Ngo, Linh, Haas, Matilda, Singer, Jeffrey, Heng, Julian Ik-Tsen
Published 2015

14-3-3ζ deficient mice in the BALB/c background display behavioural and anatomical defects associated with neurodevelopmental disorders

by Xu, Xiangjun, Jaehne, Emily J., Greenberg, Zarina, McCarthy, Peter, Saleh, Eiman, Parish, Clare L., Camera, Daria, Heng, Julian, Haas, Matilda, Baune, Bernhard T., Ratnayake, Udani, Buuse, Maarten van den, Lopez, Angel F., Ramshaw, Hayley S., Schwarz, Quenten
Published 2015

The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome

by Li, Shan Shan, Qu, Zhengdong, Haas, Matilda, Ngo, Linh, Heo, You Jeong, Kang, Hyo Jung, Britto, Joanne Maria, Cullen, Hayley Daniella, Vanyai, Hannah Kate, Tan, Seong-Seng, Chan-Ling, Tailoi, Gunnersen, Jenny Margaret, Heng, Julian Ik-Tsen
Published 2016

Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities

by Breuss, Martin, Heng, Julian Ik-Tsen, Poirier, Karine, Tian, Guoling, Jaglin, Xavier Hubert, Qu, Zhengdong, Braun, Andreas, Gstrein, Thomas, Ngo, Linh, Haas, Matilda, Bahi-Buisson, Nadia, Moutard, Marie-Laure, Passemard, Sandrine, Verloes, Alain, Gressens, Pierre, Xie, Yunli, Robson, Kathryn J.H., Rani, Deepa Selvi, Thangaraj, Kumarasamy, Clausen, Tim, Chelly, Jamel, Cowan, Nicholas Justin, Keays, David Anthony
Published 2012

De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation

by Haas, Matilda A., Ngo, Linh, Li, Shan Shan, Schleich, Sibylle, Qu, Zhengdong, Vanyai, Hannah K., Cullen, Hayley D., Cardona-Alberich, Aida, Gladwyn-Ng, Ivan E., Pagnamenta, Alistair T., Taylor, Jenny C., Stewart, Helen, Kini, Usha, Duncan, Kent E., Teleman, Aurelio A., Keays, David A., Heng, Julian I.-T.
Published 2016