Targeting AAV vectors to the central nervous system by engineering capsid-receptor interactions that enable crossing of the blood-brain barrier von Huang, Qin, Chen, Albert T, Chan, Ken Y, Sorensen, Hikari, Barry, Andrew J, Azari, Bahar, Zheng, Qingxia, Beddow, Thomas, Zhao, Binhui, Tobey, Isabelle G, Moncada-Reid, Cynthia, Eid, Fatma-Elzahraa, Walkey, Christopher J, Ljungberg, M Cecilia, Lagor, William R, Heaney, Jason D, Chan, Yujia A, Deverman, Benjamin E

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VCAM1 Is Induced in Ovarian Theca and Stromal Cells in a Mouse Model of Androgen Excess von Candelaria, Nicholes R, Padmanabhan, Achuth, Stossi, Fabio, Ljungberg, M Cecilia, Shelly, Katharine E, Pew, Braden K, Solis, Minerva, Rossano, Ayane M, McAllister, Jan M, Wu, Sheng, Richards, JoAnne S

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CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy von Ljungberg, M. Cecilia, Ali, Yousuf O., Zhu, Jie, Wu, Chia-Shan, Oka, Kazuhiro, Zhai, R. Grace, Lu, Hui-Chen

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Deletion of Porcn in Mice Leads to Multiple Developmental Defects and Models Human Focal Dermal Hypoplasia (Goltz Syndrome) von Liu, Wei, Shaver, Timothy M, Balasa, Alfred, Ljungberg, M. Cecilia, Wang, Xiaoling, Wen, Shu, Nguyen, Hoang, Van den Veyver, Ignatia B, Singh, Shree Ram

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Activation of mammalian target of rapamycin in cytomegalic neurons of human cortical dysplasia von Ljungberg, M. Cecilia, Bhattacharjee, Meenakshi B., Lu, Yaojuan, Armstrong, Dawna L., Yoshor, Daniel, Swann, John W., Sheldon, Michael, D'Arcangelo, Gabriella

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Rapamycin suppresses seizures and neuronal hypertrophy in a mouse model of cortical dysplasia von Ljungberg, M Cecilia, Sunnen, C Nicole, Lugo, Joaquin N, Anderson, Anne E, D'Arcangelo, Gabriella

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A single-cell transcriptomic map of the developing Atoh1 lineage identifies neural fate decisions and neuronal diversity in the hindbrain von Butts, Jessica C., Wu, Sih-Rong, Durham, Mark A., Dhindsa, Ryan S., Revelli, Jean-Pierre, Ljungberg, M. Cecilia, Saulnier, Olivier, McLaren, Madison E., Taylor, Michael D., Zoghbi, Huda Y.

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SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2 von Hernández-García, Andrés, Pendleton, Katherine E, Kim, Sangbae, Li, Yumei, Kim, Bum J, Zaveri, Hitisha P, Jordan, Valerie K, Berry, Aliska M, Ljungberg, M Cecilia, Chen, Rui, Lanz, Rainer B, Scott, Daryl A

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Spatial distribution of marker gene activity in the mouse lung during alveolarization von Ljungberg, M. Cecilia, Sadi, Mayce, Wang, Yunguan, Aronow, Bruce J., Xu, Yan, Kao, Rong J., Liu, Ying, Gaddis, Nathan, Ardini-Poleske, Maryanne E., Umrod, Tipparat, Ambalavanan, Namasivayam, Nicola, Teodora, Kaminski, Naftali, Ahangari, Farida, Sontag, Ryan, Corley, Richard A., Ansong, Charles, Carson, James P.

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An oocyte‐specific Cas9‐expressing mouse for germline CRISPR/Cas9‐mediated genome editing von Lanza, Denise G., Mao, Jianqiang, Lorenzo, Isabel, Liao, Lan, Seavitt, John R., Ljungberg, M. Cecilia, Simpson, Elizabeth M., DeMayo, Francesco J., Heaney, Jason D.

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Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features von Santiago-Sim, Teresa, Burrage, Lindsay C., Ebstein, Frédéric, Tokita, Mari J., Miller, Marcus, Bi, Weimin, Braxton, Alicia A., Rosenfeld, Jill A., Shahrour, Maher, Lehmann, Andrea, Cogné, Benjamin, Küry, Sébastien, Besnard, Thomas, Isidor, Bertrand, Bézieau, Stéphane, Hazart, Isabelle, Nagakura, Honey, Immken, LaDonna L., Littlejohn, Rebecca O., Roeder, Elizabeth, Afawi, Zaid, Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Craiu, Dana, De Jonghe, Peter, Guerrero-Lopez, Rosa, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Jähn, Johanna, Klein, Karl Martin, Leguern, Eric, Lerche, Holger, Marini, Carla, Muhle, Hiltrud, Rosenow, Felix, Serratosa, José, Sterbová, Katalin, Suls, Arvid, Moller, Rikke S., Striano, Pasquale, Weber, Yvonne, Zara, Federico, Kara, Bulent, Hardies, Katia, Weckhuysen, Sarah, May, Patrick, Lemke, Johannes R., Elpeleg, Orly, Abu-Libdeh, Bassam, James, Kiely N., Silhavy, Jennifer L., Issa, Mahmoud Y., Zaki, Maha S., Gleeson, Joseph G., Seavitt, John R., Dickinson, Mary E., Ljungberg, M. Cecilia, Wells, Sara, Johnson, Sara J., Teboul, Lydia, Eng, Christine M., Yang, Yaping, Kloetzel, Peter-Michael, Heaney, Jason D., Walkiewicz, Magdalena A.

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A neuronal VLDLR variant lacking the third complement-type repeat exhibits high capacity binding of apoE containing lipoproteins von Sakai, Keiko, Tiebel, Oliver, Ljungberg, M. Cecilia, Sullivan, Merry, Lee, Hye-Jeong, Terashima, Tomoya, Li, Rongying, Kobayashi, Kunihisa, Lu, Hui-Chen, Chan, Lawrence, Oka, Kazuhiro

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Multifunctional Activity-Based Protein Profiling of the Developing Lung von Stoddard, Ethan G, Volk, Regan F, Carson, James P, Ljungberg, Cecilia M, Murphree, Taylor A, Smith, Jordan N, Sadler, Natalie C, Shukla, Anil K, Ansong, Charles, Wright, Aaron T

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S100a4-Cre–mediated deletion of Ptch1 causes hypogonadotropic hypogonadism: role of pituitary hematopoietic cells in endocrine regulation von Ren, Yi Athena, Monkkonen, Teresa, Lewis, Michael T., Bernard, Daniel J., Christian, Helen C., Jorgez, Carolina J., Moore, Joshua A., Landua, John D., Chin, Haelee M., Chen, Weiqin, Singh, Swarnima, Kim, Ik Sun, Zhang, Xiang H.F., Xia, Yan, Phillips, Kevin J., MacKay, Harry, Waterland, Robert A., Ljungberg, M. Cecilia, Saha, Pradip K., Hartig, Sean M., Coll, Tatiana Fiordelisio, Richards, JoAnne S.

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Disruption of the ATXN1–CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans von Lu, Hsiang-Chih, Tan, Qiumin, Rousseaux, Maxime W C, Wang, Wei, Kim, Ji-Yoen, Richman, Ronald, Wan, Ying-Wooi, Yeh, Szu-Ying, Patel, Jay M, Liu, Xiuyun, Lin, Tao, Lee, Yoontae, Fryer, John D, Han, Jing, Chahrour, Maria, Finnell, Richard H, Lei, Yunping, Zurita-Jimenez, Maria E, Ahimaz, Priyanka, Anyane-Yeboa, Kwame, Van Maldergem, Lionel, Lehalle, Daphne, Jean-Marcais, Nolwenn, Mosca-Boidron, Anne-Laure, Thevenon, Julien, Cousin, Margot A, Bro, Della E, Lanpher, Brendan C, Klee, Eric W, Alexander, Nora, Bainbridge, Matthew N, Orr, Harry T, Sillitoe, Roy V, Ljungberg, M Cecilia, Liu, Zhandong, Schaaf, Christian P, Zoghbi, Huda Y

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Truncated apoE forms tangle-like structures in a neuronal cell line von Ljungberg, M Cecilia, Dayanandan, Rejith, Asuni, Ayodeji, Rupniak, Tom H, Anderton, Brian H, Lovestone, Simon

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S100a4-Cre-mediated deletion of Patched1 causes hypogonadotropic hypogonadism: role of pituitary hematopoietic cells in endocrine regulation von Ren, Yi Athena, Monkkonen, Teresa, Lewis, Michael T, Bernard, Daniel J, Christian, Helen C, Jorgez, Carolina J, Moore, Joshua A, Landua, John D, Chin, Haelee M, Chen, Weiqin, Singh, Swarnima, Kim, Ik Sun, Zhang, Xiang Hf, Xia, Yan, Phillips, Kevin J, MacKay, Harry, Waterland, Robert A, Ljungberg, M Cecilia, Saha, Pradip K, Hartig, Sean M, Coll, Tatiana Fiordelisio, Richards, JoAnne S

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Survival of genetically engineered, adult-derived rat astrocytes grafted into the 6-hydroxydopamine lesioned adult rat striatum von Ljungberg, M.Cecilia, Stern, Gerald, Wilkin, Graham P.

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Monitoring the intracellular fate of apolipoprotein E: Implications for Alzheimer's disease von Ljungberg, Cecilia M., Dayanandan, Rejith, Pearce, Janice, Anderton, Brian H., Lovestone, Simon

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Targeting AAV vectors to the CNS via de novo engineered capsid-receptor interactions von Huang, Qin, Chen, Albert T., Chan, Ken Y., Sorensen, Hikari, Barry, Andrew J., Azari, Bahar, Qingxia Zheng, Beddow, Thomas, Binhui Zhao, Tobey, Isabelle G., Moncada-Reid, Cynthia, Eid, Fatma-Elzahraa, Walkey, Christopher J., M. Cecilia Ljungberg, Lagor, William R., Heaney, Jason D., Chan, Yujia A., Deverman, Benjamin E.

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