Search Results - Heng, Julian

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  1. 1
    Insights into the Biology and Therapeutic Applications of Neural Stem Cells

    Insights into the Biology and Therapeutic Applications of Neural Stem Cells by Harris, L., Zalucki, O., Piper, M., Heng, Julian

    Published 2016
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  2. 2
    Brinp1 -/- mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density

    Brinp1 -/- mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density by Berkowicz, S., Featherby, T., Qu, Z., Giousoh, A., Borg, N., Heng, Julian, Whisstock, J., Bird, P.

    Published 2016
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  3. 3
    Correction to: Rp58 and p27kip1 coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex [Neural Dev. (2017);12:8.] doi: 10.1186/s13064-017-0084-3

    Correction to: Rp58 and p27kip1 coordinate cell cycle exit and neuronal migration within the embryonic mouse cerebral cortex [Neural Dev. (2017);12:8.] doi: 10.1186/s13064-017-0084... by Clément, O., Hemming, I., Gladwyn-Ng, I., Qu, Z., Li, S., Piper, M., Heng, Julian

    Published 2018
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  4. 4
    Reinforcing the association between distal 1q CNVs and structural brain disorder: A case of a complex 1q43-q44 CNV and a review of the literature

    Reinforcing the association between distal 1q CNVs and structural brain disorder: A case of a complex 1q43-q44 CNV and a review of the literature by Hemming, I., Forrest, A., Shipman, P., Woodward, K., Walsh, P., Ravine, D., Heng, Julian

    Published 2016
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  5. 5
    The zinc finger transcription factor RP58 negatively regulates Rnd2 for the control of neuronal migration during cerebral cortical development

    The zinc finger transcription factor RP58 negatively regulates Rnd2 for the control of neuronal migration during cerebral cortical development by Heng, Julian, Qu, Z., Ohtaka-Maruyama, C., Okado, H., Kasai, M., Castro, D., Guillemot, F., Tan, S.

    Published 2015
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  6. 6
    Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons

    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 2016
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  7. 7
    Neurogenic differentiation by hippocampal neural stem and progenitor cells is biased by NFIX expression

    Neurogenic differentiation by hippocampal neural stem and progenitor cells is biased by NFIX expression by Harris, L., Zalucki, O., Clément, O., Fraser, J., Matuzelski, E., Oishi, S., Harvey, T., Burne, T., Heng, Julian, Gronostajski, R., Piper, M.

    Published 2018
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  8. 8
    Mutations of vasopressin receptor 2 including novel L312S have differential effects on trafficking

    Mutations of vasopressin receptor 2 including novel L312S have differential effects on trafficking by Tiulpakov, A., White, C., Abhayawardana, R., See, H., Chan, A., Seeber, R., Heng, Julian, Dedov, I., Pavlos, N., Pfleger, K.

    Published 2016
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  9. 9
    TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons

    TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons by Ngo, L., Haas, M., Qu, Z., Li, S., Zenker, J., Teng, K., Gunnersen, J., Breuss, M., Habgood, M., Keays, D., Heng, Julian

    Published 2014
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  10. 10
    The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome

    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 2016
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  11. 11
    A review of structural brain abnormalities in Pallister-Killian syndrome

    A review of structural brain abnormalities in Pallister-Killian syndrome by Poulton, C., Baynam, Gareth, Yates, C., Alinejad-Rokny, H., Williams, S., Wright, H., Woodward, K., Sivamoorthy, S., Peverall, J., Shipman, P., Ravine, D., Beilby, J., Heng, Julian

    Published 2018
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  12. 12
    Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway

    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 2016
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  13. 13
    Transcriptional regulation of intermediate progenitor cell generation during hippocampal development

    Transcriptional regulation of intermediate progenitor cell generation during hippocampal development by Harris, L., Zalucki, O., Gobius, I., McDonald, H., Osinki, J., Harvey, T., Essebier, A., Vidovic, D., Gladwyn-Ng, I., Burne, T., Heng, Julian, Richards, L., Gronostajski, R., Piper, M.

    Published 2016
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  14. 14
    14-3-3 zeta deficient mice in the BALB/c background display behavioural and anatomical defects associated with neurodevelopmental disorders

    14-3-3 zeta deficient mice in the BALB/c background display behavioural and anatomical defects associated with neurodevelopmental disorders by Xu, X., Jaehne, E., Greenberg, Z., McCarthy, P., Saleh, E., Parish, C., Camera, D., Heng, Julian, Haas, M., Baune, B., Ratnayake, U., Van Den Buuse, M., Lopez, A., Ramshaw, H., Schwarz, Q.

    Published 2015
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  15. 15
    De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation

    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 2016
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  16. 16
    Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3

    Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3 by Sim, J., Scerri, T., Fanjul-Fernández, M., Riseley, J., Gillies, G., Pope, K., Van Roozendaal, H., Heng, Julian, Mandelstam, S., McGillivray, G., Macgregor, D., Kannan, L., Maixner, W., Harvey, A., Amor, D., Delatycki, M., Crino, P., Bahlo, M., Lockhart, P., Leventer, R.

    Published 2016
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  17. 17
    Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance

    Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance by Woodward, K., Stampalia, J., Vanyai, H., Rijhumal, H., Potts, K., Taylor, F., Peverall, J., Grumball, T., Sivamoorthy, S., Alinejad-Rokny, H., Wray, J., Whitehouse, A., Nagarajan, L., Scurlock, J., Afchani, S., Edwards, M., Murch, A., Beilby, J., Baynam, G., Kiraly-Borri, C., McKenzie, F., Heng, Julian

    Published 2019
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