Histone variant H2BE enhances chromatin accessibility in neurons to promote synaptic gene expression and long-term memory

Autor: Feierman, Emily R., Louzon, Sean, Prescott, Nicholas A., Biaco, Tracy, Gao, Qingzeng, Qiu, Qi, Choi, Kyuhyun, Palozola, Katherine C., Voss, Anna J., Mehta, Shreya D., Quaye, Camille N., Lynch, Katherine T., Fuccillo, Marc V., Wu, Hao, David, Yael, Korb, Erica

Publikováno v: In Molecular Cell 8 August 2024 84(15):2822-2837

TUBS-M and TUBS-T based modular Regolith Simulant System for the support of lunar ISRU activities

Autor: Linke, Stefan, Windisch, Lisa, Kueter, Nico, Wanvik, Jan Egil, Voss, Anna, Stoll, Enrico, Schilde, Carsten, Kwade, Arno

Publikováno v: In Planetary and Space Science January 2020 180

Fully digital workflow of an occlusal device including digital facebow record: A clinical report

Autor: Voß, Anna-Sophia, Bunz, Oskar, Kurbad, Oliver, Bürgers, Ralf

Publikováno v: In The Journal of Prosthetic Dentistry

Calving prediction in dairy cattle by visual observation or the use of technical devices

Autor: Voß, Anna Lisa

The overall objectives of this thesis were (1) to analyze the predictive performance of a calving sensor that recently became available, (2) to assess the tolerance of the sensor attachment at the animal´s tail and (3) to elicit current recommendati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5179fa1b89e6973a90c286b8b5384799

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Autor: Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S, Heung, Tracy, Holleman, Aaron M, Johnston, H Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M, Gur, Raquel E, Morrow, Bernice E, Swillen, Ann, Vorstman, Jacob AS, Bearden, Carrie E, Chow, Eva WC, van den Bree, Marianne, Emanuel, Beverly S, Vermeesch, Joris R, Warren, Stephen T, Owen, Michael J, Chopra, Pankaj, Cutler, David J, Duncan, Richard, Kotlar, Alex V, Mulle, Jennifer G, Voss, Anna J, Zwick, Michael E, Diacou, Alexander, Golden, Aaron, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Merico, Daniele, Jin, Andrea, Lilley, Brenna, Salmons, Harold I, Tran, Oanh, Holmans, Peter, Pardinas, Antonio, Walters, James TR, Demaerel, Wolfram, Boot, Erik, Butcher, Nancy J, Costain, Gregory A, Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese AMJ, van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koen, Vergaelen, Elfi, Vogels, Annick, Crowley, T Blaine, McGinn, Daniel E, Moss, Edward M, Sharkus, Robert J, Unolt, Marta, Zackai, Elaine H, Calkins, Monica E, Gallagher, Robert S, Gur, Ruben C, Tang, Sunny X, Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M, Breetvelt, Elemi, Duijff, Sasja N, Fiksinski, Ania, Moss, Hayley, Niarchou, Maria, Murphy, Kieran C, Prasad, Sarah E, Daly, Eileen M, Gudbrandsen, Maria, Murphy, Clodagh M, Murphy, Declan G, Buzzanca, Antonio, Fabio, Fabio Di, Digilio, Maria C, Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F, Ousley, Opal Y, Carmel, Miri, Gothelf, Doron, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Kushan, Leila, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stéphan, Sandini, Corrado, Schneider, Maude

Publikováno v: Molecular psychiatry, vol 26, iss 8

Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that contribute to schizophrenia, in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::32f66e4eba32686804f3949cd756407d
https://escholarship.org/uc/item/1wx189cs