Astrocytic interleukin-3 programs microglia and limits Alzheimer’s disease von McAlpine, Cameron S., Park, Joseph, Griciuc, Ana, Kim, Eunhee, Choi, Se Hoon, Iwamoto, Yoshiko, Kiss, Máté G., Christie, Kathleen A., Vinegoni, Claudio, Poller, Wolfram C., Mindur, John E., Chan, Christopher T., He, Shun, Janssen, Henrike, Wong, Lai Ping, Downey, Jeffrey, Singh, Sumnima, Anzai, Atsushi, Kahles, Florian, Jorfi, Mehdi, Feruglio, Paolo Fumene, Sadreyev, Ruslan I., Weissleder, Ralph, Kleinstiver, Benjamin P., Nahrendorf, Matthias, Tanzi, Rudolph E., Swirski, Filip K.

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Unconstrained genome targeting with near-PAMless engineered CRISPR-Cas9 variants von Walton, Russell T, Christie, Kathleen A, Whittaker, Madelynn N, Kleinstiver, Benjamin P

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Effective In Vivo Topical Delivery of siRNA and Gene Silencing in Intact Corneal Epithelium Using a Modified Cell-Penetrating Peptide von Schiroli, Davide, Gómara, María J., Maurizi, Eleonora, Atkinson, Sarah D., Mairs, Laura, Christie, Kathleen A., Cobice, Diego F., McCrudden, Cian M., Nesbit, M. Andrew, Haro, Isabel, Moore, Tara

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Making the cut with PAMless CRISPR-Cas enzymes von Christie, Kathleen A., Kleinstiver, Benjamin P.

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Listeria Phages Induce Cas9 Degradation to Protect Lysogenic Genomes von Osuna, Beatriz A., Karambelkar, Shweta, Mahendra, Caroline, Christie, Kathleen A., Garcia, Bianca, Davidson, Alan R., Kleinstiver, Benjamin P., Kilcher, Samuel, Bondy-Denomy, Joseph

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Precise DNA cleavage using CRISPR-SpRYgests von Christie, Kathleen A., Guo, Jimmy A., Silverstein, Rachel A., Doll, Roman M., Mabuchi, Megumu, Stutzman, Hannah E., Lin, Jiecong, Ma, Linyuan, Walton, Russell T., Pinello, Luca, Robb, G. Brett, Kleinstiver, Benjamin P.

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Personalised genome editing – The future for corneal dystrophies von Moore, C.B. Tara, Christie, Kathleen A., Marshall, John, Nesbit, M. Andrew

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Interleukin-3 coordinates glial-peripheral immune crosstalk to incite multiple sclerosis von Kiss, Máté G., Mindur, John E., Yates, Abi G., Lee, Donghoon, Fullard, John F., Anzai, Atsushi, Poller, Wolfram C., Christie, Kathleen A., Iwamoto, Yoshiko, Roudko, Vladimir, Downey, Jeffrey, Chan, Christopher T., Huynh, Pacific, Janssen, Henrike, Ntranos, Achilles, Hoffmann, Jan D., Jacob, Walter, Goswami, Sukanya, Singh, Sumnima, Leppert, David, Kuhle, Jens, Kim-Schulze, Seunghee, Nahrendorf, Matthias, Kleinstiver, Benjamin P., Probert, Fay, Roussos, Panos, Swirski, Filip K., McAlpine, Cameron S.

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Towards personalised allele-specific CRISPR gene editing to treat autosomal dominant disorders von Christie, Kathleen A., Courtney, David G., DeDionisio, Larry A., Shern, Connie Chao, De Majumdar, Shyamasree, Mairs, Laura C., Nesbit, M. Andrew, Moore, C. B. Tara

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Broad-spectrum anti-CRISPR proteins facilitate horizontal gene transfer von Mahendra, Caroline, Christie, Kathleen A., Osuna, Beatriz A., Pinilla-Redondo, Rafael, Kleinstiver, Benjamin P., Bondy-Denomy, Joseph

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Gene Editing for Corneal Stromal Regeneration von Moore, Tara, Chao-Shern, Connie, DeDionisio, Larry, Christie, Kathleen A., Nesbit, M. Andrew

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Mutation-Independent Allele-Specific Editing by CRISPR-Cas9, a Novel Approach to Treat Autosomal Dominant Disease von Christie, Kathleen A., Robertson, Louise J., Conway, Caroline, Blighe, Kevin, DeDionisio, Larry A., Chao-Shern, Connie, Kowalczyk, Amanda M., Marshall, John, Turnbull, Doug, Nesbit, M. Andrew, Moore, C.B. Tara

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Optimization of base editors for the functional correction of SMN2 as a treatment for spinal muscular atrophy von Alves, Christiano R. R., Ha, Leillani L., Yaworski, Rebecca, Sutton, Emma R., Lazzarotto, Cicera R., Christie, Kathleen A., Reilly, Aoife, Beauvais, Ariane, Doll, Roman M., de la Cruz, Demitri, Maguire, Casey A., Swoboda, Kathryn J., Tsai, Shengdar Q., Kothary, Rashmi, Kleinstiver, Benjamin P.

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Protein Analysis of the TGFBI R124H Mouse Model Gives Insight into Phenotype Development of Granular Corneal Dystrophy von Lukassen, Marie V, Poulsen, Ebbe T, Donaghy, Jack, Mogensen, Emilie H, Christie, Kathleen A, Roshanravan, Hila, DeDioniso, Larry, Nesbit, M Andrew, Moore, Tara, Enghild, Jan J

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Protein Analysis of the TGFBIR124H Mouse Model Gives Insight into Phenotype Development of Granular Corneal Dystrophy von Lukassen, Marie V., Poulsen, Ebbe T., Donaghy, Jack, Mogensen, Emilie H., Christie, Kathleen A., Roshanravan, Hila, DeDioniso, Larry, Nesbit, M. Andrew, Moore, Tara, Enghild, Jan J.

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Author Correction: Broad-spectrum anti-CRISPR proteins facilitate horizontal gene transfer von Mahendra, Caroline, Christie, Kathleen A., Osuna, Beatriz A., Pinilla-Redondo, Rafael, Kleinstiver, Benjamin P., Bondy-Denomy, Joseph

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NNT mediates redox-dependent pigmentation via a UVB- and MITF-independent mechanism von Allouche, Jennifer, Rachmin, Inbal, Adhikari, Kaustubh, Pardo, Luba M., Lee, Ju Hee, McConnell, Alicia M., Kato, Shinichiro, Fan, Shaohua, Kawakami, Akinori, Suita, Yusuke, Wakamatsu, Kazumasa, Igras, Vivien, Zhang, Jianming, Navarro, Paula P., Lugo, Camila Makhlouta, Noonan, Haley R., Christie, Kathleen A., Itin, Kaspar, Mujahid, Nisma, Lo, Jennifer A., Won, Chong Hyun, Evans, Conor L., Weng, Qing Yu, Wang, Hequn, Osseiran, Sam, Lovas, Alyssa, Németh, István, Cozzio, Antonio, Navarini, Alexander A., Hsiao, Jennifer J., Nguyen, Nhu, Kemény, Lajos V., Iliopoulos, Othon, Berking, Carola, Ruzicka, Thomas, Gonzalez-José, Rolando, Bortolini, Maria-Cátira, Canizales-Quinteros, Samuel, Acuna-Alonso, Victor, Gallo, Carla, Poletti, Giovanni, Bedoya, Gabriel, Rothhammer, Francisco, Ito, Shosuke, Schiaffino, Maria Vittoria, Chao, Luke H., Kleinstiver, Benjamin P., Tishkoff, Sarah, Zon, Leonard I., Nijsten, Tamar, Ruiz-Linares, Andrés, Fisher, David E., Roider, Elisabeth

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Precise DNA cleavage using CRISPR-SpRYgests von Christie, Kathleen A, Guo, Jimmy A, Silverstein, Rachel A, Doll, Roman M, Mabuchi, Megumu, Stutzman, Hannah E, Lin, Jiecong, Ma, Linyuan, Walton, Russell T, Pinello, Luca, Robb, G. Brett, Kleinstiver, Benjamin

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Astrocyte-derived interleukin-3 reprograms microglia and limits Alzheimer’s disease von McAlpine, Cameron S., Park, Joseph, Griciuc, Ana, Kim, Eunhee, Choi, Se Hoon, Iwamoto, Yoshiko, Kiss, Máté G., Christie, Kathleen A., Vinegoni, Claudio, Poller, Wolfram C., Mindur, John E., Chan, Christopher T., He, Shun, Janssen, Henrike, Wong, Lai Ping, Downey, Jeffrey, Singh, Sumnima, Anzai, Atsushi, Kahles, Florian, Jorfi, Mehdi, Feruglio, Paolo Fumene, Sadreyev, Ruslan I., Weissleder, Ralph, Kleinstiver, Benjamin P., Nahrendorf, Matthias, Tanzi, Rudolph E., Swirski, Filip K.

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Genome editing approaches to treat Spinal Muscular Atrophy von Kleinstiver, Benjamin, Christie, Kathleen A, Alves, Christiano Robles, Swoboda, Kathryn J

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