Zhengdong Qu

发表

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

Shan Shan Li, J. Singer, J. Davis, 2015, Neural Development.

Morphological and functional changes in guinea‐pig neurons projecting to the ileal mucosa at early stages after inflammatory damage

J. Furness, K. Nurgali, Billie Hunne, 2011, The Journal of physiology.

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

Shan Shan Li, A. Pagnamenta, D. Keays, 2016, Mechanisms of Development.

TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons.

Shan Shan Li, Martin W. Breuss, D. Keays, 2014, Human molecular genetics.

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

Martin W. Breuss, D. Keays, K. Thangaraj, 2012, Cell reports.

Immunohistochemical analysis of neuron types in the mouse small intestine

J. Furness, M. Bagyánszki, M. Epstein, 2008, Cell and Tissue Research.

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

Shan Shan Li, J. Britto, J. Gunnersen, 2016, Scientific Reports.

The zinc finger transcription factor RP58 negatively regulates Rnd2 for the control of neuronal migration during cerebral cortical development.

F. Guillemot, H. Okado, D. Castro, 2015, Cerebral cortex.

WD40-repeat protein 62 is a JNK-phosphorylated spindle pole protein required for spindle maintenance and timely mitotic progression

M. Bogoyevitch, J. Heng, Dominic C. H. Ng, 2012, Journal of Cell Science.

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

Shan Shan Li, J. Davis, J. Heng, 2016, Neural Development.

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

J. Whisstock, N. Borg, P. Bird, 2016, Molecular Autism.

Rp58 and p27kip1 coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex

Shan Shan Li, M. Piper, J. Heng, 2017, Neural Development.

kip 1 Rp 58 and p 27 coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex

Shan Shan Li, M. Piper, J. Heng, 2017 .

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

Shan Shan Li, A. Pagnamenta, D. Keays, 2016 .

Rp58 and p27kip1 coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex

Shan Shan Li, M. Piper, J. Heng, 2017, Neural Development.

Correction to: Rp58 and p27kip1 coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex

Shan Shan Li, M. Piper, J. Heng, 2018, Neural Development.

Perturbations in cortical development and neuronal network excitability arising from prenatal exposure to benzodiazepines in mice

C. Reid, S. Petrou, K. Campbell, 2013, The European journal of neuroscience.

CRISPR mediated somatic cell genome engineering in the chicken.

C. Marcelle, C. Hirst, Zhengdong Qu, 2015, Developmental biology.

Additional file 4: Figure S4. of Brinp1 −/− mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density

J. Whisstock, N. Borg, P. Bird, 2016 .