Search Results - Cullen, H.
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Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons by Gladwyn-Ng, I., Huang, L., Ngo, L., Li, S., Qu, Z., Vanyai, H., Cullen, H., Davis, J., Heng, Julian
Published 2016Get full text
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2
The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome by Li, S., Qu, Z., Haas, M., Ngo, L., Heo, Y., Kang, H., Britto, J., Cullen, H., Vanyai, H., Tan, S., Chan-Ling, T., Gunnersen, J., Heng, Julian
Published 2016Get full text
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3
Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway by Edvardson, S., Tian, G., Cullen, H., Vanyai, H., Ngo, L., Bhat, S., Aran, A., Daana, M., Da'amseh, N., Abu-Libdeh, B., Cowan, N., Heng, Julian, Elpeleg, O.
Published 2016Get full text
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4
De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation by Haas, M., Ngo, L., Li, S., Schleich, S., Qu, Z., Vanyai, H., Cullen, H., Cardona-Alberich, A., Gladwyn-Ng, I., Pagnamenta, A., Taylor, J., Stewart, H., Kini, U., Duncan, K., Teleman, A., Keays, D., Heng, Julian
Published 2016Get full text