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2021 Journal Article Editorial: Context-dependent regulation of neurogenesis: common themes and unique features of the neurogenic process in different model systemsLupo, Giuseppe, Piper, Michael and Zolessi, Flavio R. (2021). Editorial: Context-dependent regulation of neurogenesis: common themes and unique features of the neurogenic process in different model systems. Frontiers in Cell and Developmental Biology, 9 678475, 678475. doi: 10.3389/fcell.2021.678475 |
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2020 Journal Article Conserved epigenetic regulatory logic infers genes governing cell identityShim, Woo Jun, Sinniah, Enakshi, Xu, Jun, Vitrinel, Burcu, Alexanian, Michael, Andreoletti, Gaia, Shen, Sophie, Sun, Yuliangzi, Balderson, Brad, Boix, Carles, Peng, Guangdun, Jing, Naihe, Wang, Yuliang, Kellis, Manolis, Tam, Patrick P L, Smith, Aaron, Piper, Michael, Christiaen, Lionel, Nguyen, Quan, Bodén, Mikael and Palpant, Nathan J. (2020). Conserved epigenetic regulatory logic infers genes governing cell identity. Cell Systems, 11 (6), 625-639.e13. doi: 10.1016/j.cels.2020.11.001 |
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2020 Journal Article Missense variant contribution to USP9X-female syndromeJolly, Lachlan A., Parnell, Euan, Gardner, Alison E., Corbett, Mark A., Pérez-Jurado, Luis A., Shaw, Marie, Lesca, Gaetan, Keegan, Catherine, Schneider, Michael C., Griffin, Emily, Maier, Felicitas, Kiss, Courtney, Guerin, Andrea, Crosby, Kathleen, Rosenbaum, Kenneth, Tanpaiboon, Pranoot, Whalen, Sandra, Keren, Boris, McCarrier, Julie, Basel, Donald, Sadedin, Simon, White, Susan M., Delatycki, Martin B., Kleefstra, Tjitske, Küry, Sébastien, Brusco, Alfredo, Sukarova-Angelovska, Elena, Trajkova, Slavica, Yoon, Sehoun ... Gecz, Jozef (2020). Missense variant contribution to USP9X-female syndrome. npj Genomic Medicine, 5 (1) 53, 1-11. doi: 10.1038/s41525-020-00162-9 |
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2020 Journal Article Abnormal behavior and cortical connectivity deficits in mice lacking Usp9xKasherman, Maria A., Currey, Laura, Kurniawan, Nyoman D., Zalucki, Oressia, Vega, Michelle Sanchez, Jolly, Lachlan A., Burne, Thomas H. J., Wood, Stephen A. and Piper, Michael (2020). Abnormal behavior and cortical connectivity deficits in mice lacking Usp9x. Cerebral Cortex, 31 (3), 1763-1775. doi: 10.1093/cercor/bhaa324 |
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2020 Journal Article Alterations in gene expression in the spinal cord of mice lacking NfixMatuzelski, Elise, Essebier, Alexandra, Harris, Lachlan, Gronostajski, Richard M., Harvey, Tracey J. and Piper, Michael (2020). Alterations in gene expression in the spinal cord of mice lacking Nfix. BMC Research Notes, 13 (1) 437, 437. doi: 10.1186/s13104-020-05278-w |
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2020 Journal Article The spindle-associated microcephaly protein, WDR62, is required for neurogenesis and development of the hippocampusShohayeb, Belal, Ho, Uda Y., Hassan, Halah, Piper, Michael and Ng, Dominic C. H. (2020). The spindle-associated microcephaly protein, WDR62, is required for neurogenesis and development of the hippocampus. Frontiers in Cell and Developmental Biology, 8 549353, 549353. doi: 10.3389/fcell.2020.549353 |
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2020 Journal Article Adult neurogenesis in the olfactory system: improving performance for difficult discrimination tasks?Kouremenou, Ioanna, Piper, Michael and Zalucki, Oressia (2020). Adult neurogenesis in the olfactory system: improving performance for difficult discrimination tasks?. BioEssays, 42 (10) 2000065, 2000065. doi: 10.1002/bies.202000065 |
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2020 Journal Article The role of lipids in ependymal development and the modulation of adult neural stem cell function during aging and diseaseHarkins, Danyon, Cooper, Helen M. and Piper, Michael (2020). The role of lipids in ependymal development and the modulation of adult neural stem cell function during aging and disease. Seminars in Cell and Developmental Biology, 112, 61-68. doi: 10.1016/j.semcdb.2020.07.018 |
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2020 Journal Article Cell-extrinsic requirement for sulfate in regulating hippocampal neurogenesisZhang, Zhe, Jhaveri, Dhanisha, Sharmin, Sazia, Harvey, Tracey J., Dawson, Paul A., Piper, Michael and Simmons, David G. (2020). Cell-extrinsic requirement for sulfate in regulating hippocampal neurogenesis. Biology Open, 9 (7) bio053132, 1-7. doi: 10.1242/bio.053132 |
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2020 Journal Article Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1Oishi, Sabrina, Zalucki, Oressia, Sanchez Vega, Michelle, Harkins, Danyon, Harvey, Tracey J., Kasherman, Maria, Davila, Raul A., Hale, Lauren, White, Melissa, Piltz, Sandra, Thomas, Paul, Burne, Thomas H.J., Harris, Lachlan and Piper, Michael (2020). Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1. Genes, Brain and Behavior, 19 (4) e12637, e12637. doi: 10.1111/gbb.12637 |
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2020 Journal Article The ubiquitin system: a regulatory hub for intellectual disability and autism spectrum disorderKasherman, Maria A., Premarathne, Susitha, Burne, Thomas H. J., Wood, Stephen A. and Piper, Michael (2020). The ubiquitin system: a regulatory hub for intellectual disability and autism spectrum disorder. Molecular Neurobiology, 57 (5), 2179-2193. doi: 10.1007/s12035-020-01881-x |
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2020 Journal Article Partial loss of USP9X function leads to a male neurodevelopmental and behavioural disorder converging on TGFβ signallingJohnson, Brett V., Kumar, Raman, Oishi, Sabrina, Alexander, Suzy, Kasherman, Maria, Vega, Michelle Sanchez, Ivancevic, Atma, Gardner, Alison, Domingo, Deepti, Corbett, Mark, Parnell, Euan, Yoon, Sehyoun, Oh, Tracey, Lines, Matthew, Lefroy, Henrietta, Kini, Usha, Van Allen, Margot, Grønborg, Sabine, Mercier, Sandra, Küry, Sébastien, Bézieau, Stéphane, Pasquier, Laurent, Raynaud, Martine, Afenjar, Alexandra, Billette de Villemeur, Thierry, Keren, Boris, Désir, Julie, Van Maldergem, Lionel, Marangoni, Martina ... Undiagnosed Diseases Network (2020). Partial loss of USP9X function leads to a male neurodevelopmental and behavioural disorder converging on TGFβ signalling. Biological Psychiatry, 87 (2), 100-112. doi: 10.1016/j.biopsych.2019.05.028 |
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2020 Journal Article The association of microcephaly protein WDR62 with CPAP/IFT88 is required for cilia formation and neocortical developmentShohayeb, Belal, Ho, Uda, Yeap, Yvonne Y., Parton, Robert G., Millard, Sean S., Xu, Zhiheng, Piper, Michael and Ng, Dominic C. H. (2020). The association of microcephaly protein WDR62 with CPAP/IFT88 is required for cilia formation and neocortical development. Human Molecular Genetics, 29 (2), 248-263. doi: 10.1093/hmg/ddz281 |
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2020 Journal Article Expression of NFIA and NFIB within the murine spinal cordMatuzelski, Elise, Harvey, Tracey J., Harkins, Danyon, Nguyen, Thuan, Ruitenberg, Marc J. and Piper, Michael (2020). Expression of NFIA and NFIB within the murine spinal cord. Gene Expression Patterns, 35 119098, 119098. doi: 10.1016/j.gep.2020.119098 |
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2019 Journal Article Common Regulatory Targets of NFIA, NFIX and NFIB during Postnatal Cerebellar DevelopmentFraser, James, Essebier, Alexandra, Brown, Alexander S., Davila, Raul Ayala, Harkins, Danyon, Zalucki, Oressia, Shapiro, Lauren P., Penzes, Peter, Wainwright, Brandon J., Scott, Matthew P., Gronostajski, Richard M., Bodén, Mikael, Piper, Michael and Harvey, Tracey J. (2019). Common Regulatory Targets of NFIA, NFIX and NFIB during Postnatal Cerebellar Development. Cerebellum, 19 (1), 89-101. doi: 10.1007/s12311-019-01089-3 |
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2019 Journal Article A simple, web-based repository for the management, access and analysis of micrographic imagesDavila, Raul Ayala, Harkins, Danyon, Currey, Laura, Fraser, James, Bowles, Josephine and Piper, Michael (2019). A simple, web-based repository for the management, access and analysis of micrographic images. Journal of Molecular Histology, 50 (6), 573-580. doi: 10.1007/s10735-019-09850-y |
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2019 Journal Article Usp9X Controls Ankyrin-Repeat Domain Protein Homeostasis during Dendritic Spine DevelopmentYoon, Sehyoun, Parnell, Euan, Kasherman, Maria, Forrest, Marc P., Myczek, Kristoffer, Premarathne, Susitha, Sanchez Vega, Michelle C., Piper, Michael, Burne, Thomas H. J., Jolly, Lachlan A., Wood, Stephen A. and Penzes, Peter (2019). Usp9X Controls Ankyrin-Repeat Domain Protein Homeostasis during Dendritic Spine Development. Neuron, 105 (3), 506-521.e7. doi: 10.1016/j.neuron.2019.11.003 |
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2019 Journal Article Variants in nuclear factor I genes influence growth and developmentZenker, Martin, Bunt, Jens, Schanze, Ina, Schanze, Denny, Piper, Michael, Priolo, Manuela, Gerkes, Erica H., Gronostajski, Richard M., Richards, Linda J., Vogt, Julie, Wessels, Marja W. and Hennekam, Raoul C. (2019). Variants in nuclear factor I genes influence growth and development. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 181 (4) ajmg.c.31747, 611-626. doi: 10.1002/ajmg.c.31747 |
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2019 Journal Article The p75 neurotrophin receptor is required for the survival of neuronal progenitors and normal formation of the basal forebrain, striatum, thalamus and neocortexMeier, Sonja, Alfonsi, Fabienne, Kurniawan, Nyoman D., Milne, Michael R., Kasherman, Maria A., Delogu, Alessio, Piper, Michael and Coulson, Elizabeth J. (2019). The p75 neurotrophin receptor is required for the survival of neuronal progenitors and normal formation of the basal forebrain, striatum, thalamus and neocortex. Development, 146 (18) dev181933, dev.181933. doi: 10.1242/dev.181933 |
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2019 Conference Publication Common regulatory targets of NFIA and NFIX mediate postnatal cerebellar developmentHarvey, Tracey, Fraser, James, Essebier, Alexandra, Brown, Alexander, Davila, Raul, Boden, Mikael, Gronostajski, Richard and Piper, Michael (2019). Common regulatory targets of NFIA and NFIX mediate postnatal cerebellar development. 10th IBRO World Congress of Neuroscience, Daegu, South Korea, 21-25 September 2019. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.ibror.2019.07.1042 |
