Autophagy induction enhances TDP43 turnover and survival in neuronal ALS models von Barmada, Sami J, Serio, Andrea, Arjun, Arpana, Bilican, Bilada, Daub, Aaron, Ando, D Michael, Tsvetkov, Andrey, Pleiss, Michael, Li, Xingli, Peisach, Daniel, Shaw, Christopher, Chandran, Siddharthan, Finkbeiner, Steven

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Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations von Alami, Nael H, Smith, Rebecca B, Carrasco, Monica A, Williams, Luis A, Winborn, Christina S, Han, Steve S W, Kiskinis, Evangelos, Winborn, Brett, Freibaum, Brian D, Kanagaraj, Anderson, Clare, Alison J, Badders, Nisha M, Bilican, Bilada, Chaum, Edward, Chandran, Siddharthan, Shaw, Christopher E, Eggan, Kevin C, Maniatis, Tom, Taylor, J Paul

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Astrocyte pathology and the absence of non-cell autonomy in an induced pluripotent stem cell model of TDP-43 proteinopathy von Serio, Andrea, Bilican, Bilada, Barmada, Sami J., Ando, Dale Michael, Zhao, Chen, Siller, Rick, Burr, Karen, Haghi, Ghazal, Story, David, Nishimura, Agnes Lumi, Carrasco, Monica A., Phatnani, Hemali P., Shum, Carole, Wilmut, Ian, Maniatis, Tom, Shaw, Christopher E., Finkbeiner, Steven, Chandran, Siddharthan

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CellSIUS provides sensitive and specific detection of rare cell populations from complex single-cell RNA-seq data von Wegmann, Rebekka, Neri, Marilisa, Schuierer, Sven, Bilican, Bilada, Hartkopf, Huyen, Nigsch, Florian, Mapa, Felipa, Waldt, Annick, Cuttat, Rachel, Salick, Max R, Raymond, Joe, Kaykas, Ajamete, Roma, Guglielmo, Keller, Caroline Gubser

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Mutant induced pluripotent stem cell lines recapitulate aspects of TDP-43 proteinopathies and reveal cell-specific vulnerability von Bilican, Bilada, Serio, Andrea, Barmada, Sami J, Nishimura, Agnes Lumi, Sullivan, Gareth J, Carrasco, Monica, Phatnani, Hemali P, Puddifoot, Clare A, Story, David, Fletcher, Judy, Park, In-Hyun, Friedman, Brad A, Daley, George Q, Wyllie, David J. A, Hardingham, Giles E, Wilmut, Ian, Finkbeiner, Steven, Maniatis, Tom, Shaw, Christopher E, Chandran, Siddharthan

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Cell-mediated neuroprotection in a mouse model of human tauopathy von Hampton, David W, Webber, Daniel J, Bilican, Bilada, Goedert, Michel, Spillantini, Maria Grazia, Chandran, Siddharthan

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Signaling Pathways Controlling Pluripotency and Early Cell Fate Decisions of Human Induced Pluripotent Stem Cells von Vallier, Ludovic, Touboul, Thomas, Brown, Stephanie, Cho, Candy, Bilican, Bilada, Alexander, Morgan, Cedervall, Jessica, Chandran, Siddharthan, Ährlund‐Richter, Lars, Weber, Anne, Pedersen, Roger A.

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Evidence for evolutionary divergence of activity-dependent gene expression in developing neurons von Qiu, Jing, McQueen, Jamie, Bilican, Bilada, Dando, Owen, Magnani, Dario, Punovuori, Karolina, Selvaraj, Bhuvaneish T, Livesey, Matthew, Haghi, Ghazal, Heron, Samuel, Burr, Karen, Patani, Rickie, Rajan, Rinku, Sheppard, Olivia, Kind, Peter C, Simpson, T Ian, Tybulewicz, Victor Lj, Wyllie, David Ja, Fisher, Elizabeth Mc, Lowell, Sally, Chandran, Siddharthan, Hardingham, Giles E

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Physiological normoxia and absence of EGF is required for the long-term propagation of anterior neural precursors from human pluripotent cells von Bilican, Bilada, Livesey, Matthew R, Haghi, Ghazal, Qiu, Jing, Burr, Karen, Siller, Rick, Hardingham, Giles E, Wyllie, David J A, Chandran, Siddharthan

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Maturation of AMPAR composition and the GABAAR reversal potential in hPSC-derived cortical neurons von Livesey, Matthew R, Bilican, Bilada, Qiu, Jing, Rzechorzek, Nina M, Haghi, Ghazal, Burr, Karen, Hardingham, Giles E, Chandran, Siddharthan, Wyllie, David J A

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Allele-specific knockdown of ALS-associated mutant TDP-43 in neural stem cells derived from induced pluripotent stem cells von Nishimura, Agnes L, Shum, Carole, Scotter, Emma L, Abdelgany, Amr, Sardone, Valentina, Wright, Jamie, Lee, Youn-Bok, Chen, Han-Jou, Bilican, Bilada, Carrasco, Monica, Maniatis, Tom, Chandran, Siddharthan, Rogelj, Boris, Gallo, Jean-Marc, Shaw, Christopher E

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A proteogenomic view of Parkinson’s disease causality and heterogeneity von Kaiser, Sergio, Zhang, Luqing, Mollenhauer, Brit, Jacob, Jaison, Longerich, Simonne, Del-Aguila, Jorge, Marcus, Jacob, Raghavan, Neha, Stone, David, Fagboyegun, Olumide, Galasko, Douglas, Dakna, Mohammed, Bilican, Bilada, Dovlatyan, Mary, Kostikova, Anna, Li, Jingyao, Peterson, Brant, Rotte, Michael, Sanz, Vinicius, Foroud, Tatiana, Hutten, Samantha J., Frasier, Mark, Iwaki, Hirotaka, Singleton, Andrew, Marek, Ken, Crawford, Karen, Elwood, Fiona, Messa, Mirko, Serrano-Fernandez, Pablo

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Induction of Olig2 precursors by FGF involves BMP signalling blockade at the Smad level von Bilican, Bilada, Fiore-Heriche, Christelle, Compston, Alastair, Allen, Nicholas D, Chandran, Siddharthan

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Neural Precursor Cells Cultured at Physiologically Relevant Oxygen Tensions Have a Survival Advantage Following Transplantation von Stacpoole, Sybil R.L., Webber, Daniel J., Bilican, Bilada, Compston, Alastair, Chandran, Siddharthan, Franklin, Robin J.M.

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Genetic Ablation of AXL Does Not Protect Human Neural Progenitor Cells and Cerebral Organoids from Zika Virus Infection von Wells, Michael F., Salick, Max R., Wiskow, Ole, Ho, Daniel J., Worringer, Kathleen A., Ihry, Robert J., Kommineni, Sravya, Bilican, Bilada, Klim, Joseph R., Hill, Ellen J., Kane, Liam T., Ye, Chaoyang, Kaykas, Ajamete, Eggan, Kevin

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Saccharomyces cerevisiae C1D is implicated in both non‐homologous DNA end joining and homologous recombination von Erdemir, Tuba, Bilican, Bilada, Cagatay, Tolga, Goding, Colin R., Yavuzer, Ugur

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Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2 von Bell, Karen F.S., Al-Mubarak, Bashayer, Martel, Marc-André, McKay, Sean, Wheelan, Nicola, Hasel, Philip, Márkus, Nóra M., Baxter, Paul, Deighton, Ruth F., Serio, Andrea, Bilican, Bilada, Chowdhry, Sudhir, Meakin, Paul J., Ashford, Michael L.J., Wyllie, David J.A., Scannevin, Robert H., Chandran, Siddharthan, Hayes, John D., Hardingham, Giles E.

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Human iPSC and CRISPR targeted gene knock-in strategy for studying the somatic TIE2L914F mutation in endothelial cells von Lazovic, Bojana, Nguyen, Hoang-Tuan, Ansarizadeh, Mohammadhassan, Wigge, Leif, Kohl, Franziska, Li, Songyuan, Carracedo, Miguel, Kettunen, Jere, Krimpenfort, Luc, Elgendy, Ramy, Richter, Kati, De Silva, Laknee, Bilican, Bilada, Singh, Prateek, Saxena, Pratik, Jakobsson, Lars, Hong, Xuechong, Eklund, Lauri, Hicks, Ryan

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Human iPSC and CRISPR targeted gene knock-in strategy for studying the somatic TIE2 L914F mutation in endothelial cells von Lazovic, Bojana, Nguyen, Hoang-Tuan, Ansarizadeh, Mohammadhassan, Wigge, Leif, Kohl, Franziska, Li, Songyuan, Carracedo, Miguel, Kettunen, Jere, Krimpenfort, Luc, Elgendy, Ramy, Richter, Kati, De Silva, Laknee, Bilican, Bilada, Singh, Prateek, Saxena, Pratik, Jakobsson, Lars, Hong, Xuechong, Eklund, Lauri, Hicks, Ryan

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Correction: Human iPSC and CRISPR targeted gene knock-in strategy for studying the somatic TIE2L914F mutation in endothelial cells von Lazovic, Bojana, Nguyen, Hoang-Tuan, Ansarizadeh, Mohammadhassan, Wigge, Leif, Kohl, Franziska, Li, Songyuan, Carracedo, Miguel, Kettunen, Jere, Krimpenfort, Luc, Elgendy, Ramy, Richter, Kati, De Silva, Laknee, Bilican, Bilada, Singh, Prateek, Saxena, Pratik, Jakobsson, Lars, Hong, Xuechong, Eklund, Lauri, Hicks, Ryan

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