Autism-associated mutations in the CaVβ2 calcium-channel subunit increase Ba2+-currents and lead to differential modulation by the RGK-protein Gem von Despang, Patrick, Salamon, Sarah, Breitenkamp, Alexandra F., Kuzmenkina, Elza, Herzig, Stefan, Matthes, Jan

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Circuits that encode and guide alcohol-associated preference von Scaplen, Kristin M, Talay, Mustafa, Nunez, Kavin M, Salamon, Sarah, Waterman, Amanda G, Gang, Sydney, Song, Sophia L, Barnea, Gilad, Kaun, Karla R

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CaM-dependent modulation of human Ca V 1.3 whole-cell and single-channel currents by C-terminal CaMKII phosphorylation site S1475 von Salamon, Sarah, Kuzmenkina, Elza, Fried, Cora, Matthes, Jan

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CaM‐dependent modulation of human CaV1.3 whole‐cell and single‐channel currents by C‐terminal CaMKII phosphorylation site S1475 von Salamon, Sarah, Kuzmenkina, Elza, Fried, Cora, Matthes, Jan

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Inactivation induced by pathogenic Ca v 1.3 L‐type Ca 2+ ‐channel variants enhances sensitivity for dihydropyridine Ca 2+ channel blockers von Török, Ferenc, Salamon, Sarah, Ortner, Nadine J., Fernández‐Quintero, Monica L., Matthes, Jan, Striessnig, Jörg

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Test-retest reliability of the diagnosis of schizoaffective disorder in childhood and adolescence – A systematic review and meta-analysis von Salamon, Sarah, Santelmann, Hanno, Franklin, Jeremy, Baethge, Christopher

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Inhibitory effects on L- and N-type calcium channels by a novel CaVβ1 variant identified in a patient with autism spectrum disorder von Despang, Patrick, Salamon, Sarah, Breitenkamp, Alexandra, Kuzmenkina, Elza, Matthes, Jan

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Inactivation induced by pathogenic Cav1.3 L‐type Ca2+‐channel variants enhances sensitivity for dihydropyridine Ca2+ channel blockers von Török, Ferenc, Salamon, Sarah, Ortner, Nadine J., Fernández‐Quintero, Monica L., Matthes, Jan, Striessnig, Jörg

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Inactivation induced by pathogenic Ca v 1.3 L-type Ca 2+ -channel variants enhances sensitivity for dihydropyridine Ca 2+ channel blockers von Török, Ferenc, Salamon, Sarah, Ortner, Nadine J, Fernández-Quintero, Monica L, Matthes, Jan, Striessnig, Jörg

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Inhibitory effects on L- and N-type calcium channels by a novel Ca V β 1 variant identified in a patient with autism spectrum disorder von Despang, Patrick, Salamon, Sarah, Breitenkamp, Alexandra, Kuzmenkina, Elza, Matthes, Jan

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CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly von Sukumaran, Salil K., Stumpf, Maria, Salamon, Sarah, Ahmad, Ilyas, Bhattacharya, Kurchi, Fischer, Sarah, Müller, Rolf, Altmüller, Janine, Budde, Birgit, Thiele, Holger, Tariq, Muhammad, Malik, Naveed Altaf, Nürnberg, Peter, Baig, Shahid Mahmood, Hussain, Muhammad Sajid, Noegel, Angelika A.

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Autism-associated mutations in the Ca V β 2 calcium-channel subunit increase Ba 2+ -currents and lead to differential modulation by the RGK-protein Gem von Despang, Patrick, Salamon, Sarah, Breitenkamp, Alexandra F, Kuzmenkina, Elza, Herzig, Stefan, Matthes, Jan

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Dung‐visiting beetle diversity is mainly affected by land use, while community specialization is driven by climate von Englmeier, Jana, Hoermann, Christian, Rieker, Daniel, Benbow, Marc Eric, Benjamin, Caryl, Fricke, Ute, Ganuza, Cristina, Haensel, Maria, Lackner, Tomáš, Mitesser, Oliver, Redlich, Sarah, Riebl, Rebekka, Rojas‐Botero, Sandra, Rummler, Thomas, Salamon, Jörg‐Alfred, Sommer, David, Steffan‐Dewenter, Ingolf, Tobisch, Cynthia, Uhler, Johannes, Uphus, Lars, Zhang, Jie, Müller, Jörg

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Subdiffusive motion of bacteriophage in mucosal surfaces increases the frequency of bacterial encounters von Barr, Jeremy J., Auro, Rita, Sam-Soon, Nicholas, Kassegne, Sam, Peters, Gregory, Bonilla, Natasha, Hatay, Mark, Mourtada, Sarah, Bailey, Barbara, Youle, Merry, Felts, Ben, Baljon, Arlette, Nulton, Jim, Salamon, Peter, Rohwer, Forest

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Insulin receptor signaling engages bladder urothelial defenses that limit urinary tract infection von Schwartz, Laura, Salamon, Kristin, Simoni, Aaron, Eichler, Tad, Jackson, Ashley R., Murtha, Matthew, Becknell, Brian, Kauffman, Andrew, Linn-Peirano, Sarah, Holdsworth, Natalie, Tyagi, Vidhi, Tang, Hancong, Rust, Steve, Cortado, Hanna, Zabbarova, Irina, Kanai, Anthony, Spencer, John David

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Analysing the influence of dapagliflozin on urinary tract infection vulnerability and kidney injury in mice infected with uropathogenic Escherichia coli von Salamon, Kristin, Linn‐Peirano, Sarah, Simoni, Aaron, Dios Ruiz‐Rosado, Juan, Becknell, Brian, John, Preeti, Schwartz, Laura, Spencer, John David

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Adjuvant haploidentical virus-specific T lymphocytes for treatment of disseminated adenovirus infection in a premature infant von Auletta, Jeffery J., Sánchez, Pablo J., Meyer, Erin K., O'Donnell, Lynn C., Cassady, Kevin A., Ouellette, Christopher P., Hecht, Shaina, Diaz, Alejandro, Pavlek, Leeann R., Salamon, Douglas P., Gallagher, Christina L., Bradbury, Hillary, Welfley, Sarah L., Magers, Jacqueline, Armbruster, Debra L., Lamb, Margaret G., Nakkula, Robin J., Bosse, Kevin, Lee, Dean A.

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Magnetic control of flexoelectric domains in a nematic fluid von Salamon, Péter, Éber, Nándor, Buka, Ágnes, Ostapenko, Tanya, Dölle, Sarah, Stannarius, Ralf

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IRF2BPL Is Associated with Neurological Phenotypes von Marcogliese, Paul C., Rosenfeld, Jill A., Koenig, Mary Kay, Chen, Agnes H., Dickson, Patricia I., Vera, Moin U., Salamon, Noriko, Infante, Elena, Poppe, Bruce, Chung, Hyung-Lok, Zuo, Zhongyuan, Kanca, Oguz, Xia, Fan, Smith, Edward C., Jasien, Joan, Kansagra, Sujay, Lark, Robert, Riley, Kacie, Golden-Grant, Katie, Poppe, Bruce, Terryn, Wim, Adams, David R., Allard, Patrick, Bacino, Carlos A., Bick, David P., Bostwick, Bret L., Brush, Matthew, Burrage, Lindsay C., Clark, Gary D., Cooper, Cynthia M., D’Souza, Precilla, Davids, Mariska, Dell’Angelica, Esteban C., Dhar, Shweta U., Dillon, Ani, Dorrani, Naghmeh, Dorset, Daniel C., Esteves, Cecilia, Fogel, Brent L., Gahl, William A., Gourdine, Jean-Philippe F., Haendel, Melissa, Hamid, Rizwan, Hanchard, Neil A., Howerton, Ellen M., Jiang, Yong-hui, Johnston, Jean M., Krier, Joel B., Lalani, Seema R., Lau, C. Christopher, Lee, Brendan H., Levy, Shawn E., Lewis, Richard A., Lipson, Allen, Loo, Sandra K., Macnamara, Ellen F., MacRae, Calum A., Manolio, Teri A., Martínez-Agosto, Julian A., McConkie-Rosell, Allyn, McCormack, Colleen E., Morimoto, Marie, Mulvihill, John J., Muzny, Donna M., Nelson, Stan F., Newberry, J. Scott, Nicholas, Sarah K., Pallais, J. Carl, Palmer, Christina G.S., Papp, Jeanette C., Parker, Neil H., Phillips, John A., Posey, Jennifer E., Postlethwait, John H., Potocki, Lorraine, Robertson, Amy K., Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Smith, Kevin S., Splinter, Kimberly, Stoler, Joan M., Sweetser, David A., Toro, Camilo, Urv, Tiina K., Vilain, Eric, Vogel, Tiphanie P., Wahl, Colleen E., Walley, Nicole M., Walsh, Chris A., Waters, Katrina M., Westerfield, Monte, Yu, Guoyun, Zheng, Allison, Yamamoto, Shinya, Wangler, Michael F., Lee, Brendan, Nelson, Stanley F., Goldstein, David B., Bellen, Hugo J.

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DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies von Ji, Jianling, Lee, Hane, Argiropoulos, Bob, Dorrani, Naghmeh, Mann, John, Martinez-Agosto, Julian A, Gomez-Ospina, Natalia, Gallant, Natalie, Bernstein, Jonathan A, Hudgins, Louanne, Slattery, Leah, Isidor, Bertrand, Le Caignec, Cédric, David, Albert, Obersztyn, Ewa, Wiśniowiecka-Kowalnik, Barbara, Fox, Michelle, Deignan, Joshua L, Vilain, Eric, Hendricks, Emily, Horton Harr, Margaret, Noon, Sarah E, Jackson, Jessi R, Wilkens, Alisha, Mirzaa, Ghayda, Salamon, Noriko, Abramson, Jeff, Zackai, Elaine H, Krantz, Ian, Innes, A Micheil, Nelson, Stanley F, Grody, Wayne W, Quintero-Rivera, Fabiola

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