Rp58 and p27(kip1) coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex

por Clément, Olivier, Hemming, Isabel Anne, Gladwyn-Ng, Ivan Enghian, Qu, Zhengdong, Li, Shan Shan, Piper, Michael, Heng, Julian Ik-Tsen
Publicado 2017

Correction to: Rp58 and p27(kip1) coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex

por Clément, Olivier, Hemming, Isabel Anne, Gladwyn-Ng, Ivan Enghian, Qu, Zhengdong, Li, Shan Shan, Piper, Michael, Heng, Julian Ik-Tsen
Publicado 2018

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

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

Brinp1(−/−) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density

por Berkowicz, Susan R., Featherby, Travis J., Qu, Zhengdong, Giousoh, Aminah, Borg, Natalie A., Heng, Julian I., Whisstock, James C., Bird, Phillip I.
Publicado 2016

Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons

por Gladwyn-Ng, Ivan, Huang, Lieven, Ngo, Linh, Li, Shan Shan, Qu, Zhengdong, Vanyai, Hannah Kate, Cullen, Hayley Daniella, Davis, John Michael, Heng, Julian Ik-Tsen
Publicado 2016

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

por 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
Publicado 2016

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

por 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.
Publicado 2016

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

por 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
Publicado 2012