Interleukin 6 reduces allopregnanolone synthesis in the brain and contributes to age-related cognitive decline in mice von Parks, Eileen E., Logan, Sreemathi, Yeganeh, Alexander, Farley, Julie A., Owen, Daniel B., Sonntag, William E.

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Insulin-like growth factor receptor signaling regulates working memory, mitochondrial metabolism, and amyloid-β uptake in astrocytes von Logan, Sreemathi, Pharaoh, Gavin A., Marlin, M. Caleb, Masser, Dustin R., Matsuzaki, Satoshi, Wronowski, Benjamin, Yeganeh, Alexander, Parks, Eileen E., Premkumar, Pavithra, Farley, Julie A., Owen, Daniel B., Humphries, Kenneth M., Kinter, Michael, Freeman, Willard M., Szweda, Luke I., Van Remmen, Holly, Sonntag, William E.

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Cell Surface Epidermal Growth Factor Receptors Increase Src and c-Cbl Activity and Receptor Ubiquitylation von Parks, Eileen E., Ceresa, Brian P.

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Human GGT2 does not autocleave into a functional enzyme: A cautionary tale for interpretation of microarray data on redox signaling von West, Matthew B, Wickham, Stephanie, Parks, Eileen E, Sherry, David M, Hanigan, Marie H

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MMP-2 expression by fibroblasts is suppressed by the myofibroblast phenotype von Howard, Eric W., Crider, Beverly J., Updike, Dawn L., Bullen, Elizabeth C., Parks, Eileen E., Haaksma, Carol J., Sherry, David M., Tomasek, James J.

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A simple method for using silicone elastomer masks for quantitative analysis of cell migration without cellular damage or substrate disruption von Sherry, David M, Parks, Eileen E, Bullen, Elizabeth C, Updike, Dawn L, Howard, Eric W

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Comparing the effects of growth hormone and IGF-1 signaling on spatial learning and memory von Ashpole, Nicole M., Logan, Sreemathi, Parks, Eileen E., Hodges, Erik L., Owen, Daniel B., Farley, Julie A., Sonntag, William E.

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Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus Statement von Khong, T Yee, Mooney, Eoghan E, Ariel, Ilana, Balmus, Nathalie C M, Boyd, Theonia K, Brundler, Marie-Anne, Derricott, Hayley, Evans, Margaret J, Faye-Petersen, Ona M, Gillan, John E, Heazell, Alex E P, Heller, Debra S, Jacques, Suzanne M, Keating, Sarah, Kelehan, Peter, Maes, Ann, McKay, Eileen M, Morgan, Terry K, Nikkels, Peter G J, Parks, W Tony, Redline, Raymond W, Scheimberg, Irene, Schoots, Mirthe H, Sebire, Neil J, Timmer, Albert, Turowski, Gitta, van der Voorn, J Patrick, van Lijnschoten, Ineke, Gordijn, Sanne J

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Marine infectious disease dynamics and outbreak thresholds: contact transmission, pandemic infection, and the potential role of filter feeders von Bidegain, Gorka, Powell, Eric N., Klinck, John M., Ben‐Horin, Tal, Hofmann, Eileen E., Park, A.

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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study von Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R, Bateman, Mark, Best, Sunayna K, Campbell, Carolyn, Carey, Georgina, Chitty, Lyn S, Cilliers, Deirdre, Cohen, Kelly, Collingwood, Emma, Constantinou, Panayiotis, Cresswell, Lara, Delmege, Catherine, Edwards, Sandra L, Ellis, Richard, Evans, Jerry, Everett, Thomas, Pinto, Clare F, Forrester, Natalie, Fowler, Emma, Gardiner, Carol, Hamilton, Susan, Healey, Karen, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Hudson, Rebecca, Hurles, Matthew E, Jenkins, Lucy, Keelagher, Rebecca, Kilby, Mark D, Lester, Tracey, Lewis, Rebecca, Lord, Jenny, Maher, Eamonn R, Marton, Tamas, McMullan, Dominic J, Mehta, Sarju, Mellis, Rhiannon, Newbury-Ecob, Ruth, Park, Soo-Mi, Parker, Michael, Prescott, Katrina, Prigmore, Elena, Quarrell, Oliver W, Quinlan-Jones, Elizabeth, Ramsden, Simon C, Rinck, Gabriele, Robart, Sarah, Roberts, Eileen, Rowland, Jayne, Steer, James, Tapon, Dagmar, Taylor, Emma J, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Williams, Denise, Wilson, Elizabeth

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Use, Durability, and Risks for Discontinuation of Initial and Subsequent Biologics in a Large Pediatric‐Onset IBD Cohort von Kaplan, Jess L., Liu, Chunyan, King, Eileen C., Bass, Julie A., Patel, Ashish S., Tung, Jeanne, Chen, Shiran, Lissoos, Trevor, Candela, Ninfa, Saeed, Shehzad, Colletti, Richard B., Adler, Jeremy, Baron, Howard I., Cabrera, José M., Dorsey, Jill M., Dykes, Dana M.H., Ebach, Dawn R., Garin‐Laflam, Monica P., Gold, Benjamin D., Grunow, John, Higuchi, Leslie M., Jester, Traci W., Lapsia, Sameer P., Leibowitz, Ian, Linvlle, Tiffany M., Morhardt, Tina L., Moses, Jonathan, Moulton, Dedrick, Nasiri‐Blomgren, Shaida, Niklinska‐Schirtz, B. Joanna, Ogunmola, Nicholas A., Palomo, Pablo J., Park, K.T., Pashankar, Dinesh S., Pasternak, Brad A., Radano, Marcella C., Samson, Charles M., Sandberg, Kelly C., Schaefer, Marc E., Shashidhar, Harohalli, Steiner, Steven J., Sullivan, Jillian S., Tomer, Gitit, Verstraete, Sophia G.

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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies von Appenzeller, Silke, Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, De Jonghe, Peter, Depienne, Christel, Dimova, Petia, Djémié, Tania, Gormley, Padhraig, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Kuhlenbäumer, Gregor, Lemke, Johannes R., Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Møller, Rikke S., Muhle, Hiltrud, Palotie, Aarno, Pendziwiat, Manuela, Roelens, Filip, Rosenow, Felix, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Abou-Khalil, Bassel, Alldredge, Brian K., Andermann, Eva, Andermann, Frederick, Amron, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alex, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Knowlton, Robert C., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Singh, Rani, Smith, Michael C., Sullivan, Joe, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Winawer, Melodie R., Cossette, Patrick, Delanty, Norman, Eichler, Evan E., Goldstein, David B., Han, Yujun, Heinzen, Erin L., Marson, Anthony G., Nieh, Sahar Esmaeeli, O’Brien, Terence J., Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K.

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Randomized, Controlled Trial of an Advance Care Planning Video Decision Support Tool for Patients With Advanced Heart Failure von El-Jawahri, Areej, Paasche-Orlow, Michael K, Matlock, Dan, Stevenson, Lynne Warner, Lewis, Eldrin F, Stewart, Garrick, Semigran, Marc, Chang, Yuchiao, Parks, Kimberly, Walker-Corkery, Elizabeth S, Temel, Jennifer S, Bohossian, Hacho, Ooi, Henry, Mann, Eileen, Volandes, Angelo E

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Diverse genetic causes of polymicrogyria with epilepsy von Allen, Andrew S, Aggarwal, Vimla, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Guerrini, Renzo, Glauser, Tracy, Heinzen, Erin L, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Poduri, Annapurna, Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Abou‐Khalil, Bassel, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Cascino, Greg, Consalvo, Damian, Crumrine, Pat, Devinsky, Orrin, Dlugos, Dennis, Fountain, Nathan, Freyer, Catharine, Friedman, Dan, Geller, Eric, Glynn, Simon, Haas, Kevin, Haut, Sheryl, Joshi, Sucheta, Kirsch, Heidi, Knowlton, Robert, Kossoff, Eric, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Poduri, Annapurna, Scheffer, Ingrid, Shellhaas, Renée A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sperling, Michael, Smith, Michael C., Sullivan, Joseph, Vining, Eileen P. G., Von Allmen, Gretchen K., Widdess‐Walsh, Peter, Winawer, Melodie R., Bautista, Jocelyn, Fiol, Miguel, Glauser, Tracy, Hayward, Jean, Helmers, Sandra, Park, Kristen, Sirven, Joseph, Lin Thio, Liu, Venkat, Anu, Weisenberg, Judith, Kuperman, Rachel, McGuire, Shannon, Novotny, Edward, Sadleir, Lynette

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Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy von Allen, Andrew S., Berkovic, Samuel F., Coe, Bradley P., Cook, Joseph, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Goldstein, David B., Heinzen, Erin L., Johnson, Michael R., Krumm, Nik, Kuzniecky, Ruben, Lowenstein, Daniel H., Marson, Anthony G., Mefford, Heather C., Nelson, Ben, Esmaeeli Nieh, Sahar, O'Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Petrovski, Slavé, Poduri, Annapurna, Raja, Archana, Ruzzo, Elizabeth K., Scheffer, Ingrid E., Sherr, Elliott, Abou‐Khalil, Bassel, Alldredge, Brian K., Andermann, Eva, Andermann, Frederick, Amron, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Boro, Alex, Cascino, Gregory, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, Fountain, Nathan B., French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E., Knowlton, Robert C., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., McGuire, Shannon M., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Poduri, Annapurna, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Shih, Jerry J., Singh, Rani, Sirven, Joseph, Smith, Michael C., Sullivan, Joe, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Widdess‐Walsh, Peter, Winawer, Melodie R.

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The Lifestyle Interventions and Independence for Elders Study: Design and Methods von Fielding, Roger A., Rejeski, W. Jack, Blair, Steven, Church, Tim, Espeland, Mark A., Gill, Thomas M., Guralnik, Jack M., Hsu, Fang-Chi, Katula, Jeffrey, King, Abby C., Kritchevsky, Stephen B., McDermott, Mary M., Miller, Michael E., Nayfield, Susan, Newman, Anne B., Williamson, Jeff D., Bonds, Denise, Romashkan, Sergei, Hadley, Evan, Pahor, Marco

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HLA-DRB111 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis von Ombrello, Michael J, Remmers, Elaine F, Tachmazidou, Ioanna, Grom, Alexei, Foell, Dirk, Haas, Johannes-Peter, Martini, Alberto, Gattorno, Marco, Özen, Seza, Prahalad, Sampath, Zeft, Andrew S, Bohnsack, John F, Mellins, Elizabeth D, Ilowite, Norman T, Russo, Ricardo, Len, Claudio, Hilario, Maria Odete E, Oliveira, Sheila, Yeung, Rae S M, Rosenberg, Alan, Wedderburn, Lucy R, Anton, Jordi, Schwarz, Tobias, Hinks, Anne, Bilginer, Yelda, Park, Jane, Cobb, Joanna, Satorius, Colleen L, Han, Buhm, Baskin, Elizabeth, Signa, Sara, Duerr, Richard H, Achkar, J P, Kamboh, M Ilyas, Kaufman, Kenneth M, Kottyan, Leah C, Pinto, Dalila, Scherer, Stephen W, Alarcón-Riquelme, Marta E, Docampo, Elisa, Estivill, Xavier, Gül, Ahmet, de Bakker, Paul I W, Raychaudhuri, Soumya, Langefeld, Carl D, Thompson, Susan, Zeggini, Eleftheria, Thomson, Wendy, Kastner, Daniel L, Woo, Patricia

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Stereoacuity in children with anisometropic amblyopia von Wallace, David K., MD, MPH, Lazar, Elizabeth L., MS, MPH, Melia, Michele, ScM, Birch, Eileen E., PhD, Holmes, Jonathan M., BM, BCh, Hopkins, Kristine B., OD, MSPH, Kraker, Raymond T., MSPH, Kulp, Marjean T., OD, MS, Pang, Yi, PhD, OD, Repka, Michael X., MD, MBA, Tamkins, Susanna M., OD, Weise, Katherine K., OD, MBA

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Lack of effect of benralizumab on signs and symptoms of moderate‐to‐severe atopic dermatitis: Results from the phase 2 randomized, double‐blind, placebo‐controlled HILLIER trial... von Guttman‐Yassky, E., Brooks, L., Clark, K. L., Grindebacke, H., Ho, C. N., Katial, R., Pham, T.‐H., Walton, C., Guttman‐Yassky, Emma, Gómez Arias, Pedro Jesús, Alpizar, Ricardo, Alpizar, Sady, Asrenberger, Petr, Azib, Selma, Badia, Anais, Beck, Lisa, Bran, Eduardo Lopez, Breneman, Debra, Brezoev, Petyo, Calatayud, Antonio Martorell, Calderin, Yendrys, Choi, Hoon, Choi, Myoung Eun, Chwała, Cezary, Crespo, Esther Roe, Czajkowski, Rafal, Dezoteux, Frédéric, Fiserova, Nadezda, Godwin, Loyd, Grigoryan, Diana, Hofman, Anna, Hofman, Teresa, Honigman, Anthony, Jang, Yong Hyun, Jarell, Abel, Kaczmarek, Barbara, Kaščáková, Zuzana, Kern, Johannes, Klein, Ryan, Ko, Hyun Chang, Matin, Jasmin, Komárková, Klaudie, Laageide, Leah, Lam, Yaohan, Lee, Yang Won, Leflein, Jeffrey, Lynn, Lon D., Mandazhieva‐Pepelanova, Mariana, Misery, Laurent, Murrell, Dedee, Musiał, Kamila, Na, Chan Ho, Na, Jung Im, O’Connor, Sarah, Owczarek, Witold, Park, Chun Wook, Pełka, Karolina, Pulka, Grazyna, Puzas, Álvaro Iglesias, Ruiz, Juan Alberto Ruano, Sabaday, Zach, Salvador, Juan Francisco Silvestre, Sanz‐Motilva, Virgnia, Schleicher, Stephen, Scott, Robert, Seo, Seong Jun, Son, Hyung Seok, Son, Sang Wook, Spelman, Lynda, Staumont‐Salle, Delphine, Stefanski, Marion, Supranowicz, Madeleine, Tan, Ricardo, Vaneckova, Jaroslava, Vantuchova, Yvetta, Vasilev, Ivaylo, Vasileva, Irida, Vekovska, Kamelia, Zajicova, Sylva, Aldridge, Sarah, Babcock, Eileen, Barker, Peter, Betlińska, Zuzanna, Duncan, Marnie, Empati, Rama, Jison, Maria, Kwiatek, Justin, Maho, Emmanuelle, McAlexander, Allen, McCrae, Christopher, Melville, Margaret, Natkańska, Urszula, Ndamira, Apollo, Reddy, Yasa, Regan, Scott, Rodríguez‐Suárez, Eva, Rusiecka, Anna, Shen, David, Svärd, Magnus Bergman, Zaborowska, Urszula

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The role of copy number variants in the genetic architecture of common familial epilepsies von Almanza Fuerte, Edith P., Nguyen, John, Mehaffey, Michelle, Sulovari, Arvis, Wang, Tianyun, Galey, Miranda, Miller, Danny E., Eichler, Evan E., Mefford, Heather C., Abou‐Khalil, Bassel, Afawi, Zaid Afawi, Allen, Andrew S., Amrom, Dina, Andermann, Eva, Bautista, Jocelyn F., Bellows, Susannah T., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Burgess, Rosemary, Cascino, Gregory D., Chung, Seo‐Kyung, Consalvo, Damian, Cossette, Patrick, Crompton, Douglas E., Crumrine, Patricia, Curtis, Sarah W., Delanty, Norman, Devinsky, Orrin, Dlugos, Dennis, Ellis, Colin A., Epstein, Michael P., Fiol, Miguel, Fountain, Nathan B., Freyer, Catharine, Friedman, Dan, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gravel, Micheline, Haas, Kevin, Harris, Rebekah V., Haut, Sheryl, Heinzen, Erin L., Helmers, Sandra, Henry, Olivia J., Joshi, Sucheta, Kirsch, Heidi E., Kivity, Sara, Knowlton, Robert C., Kossoff, Eric, Kuzniecky, Ruben, Loeb, Rebecca, Lowenstein, Daniel H., Marson, Anthony G., McCormack, Mark, McGuire, Shannon M., McKenna, Kevin, Motika, Paul V., Mullen, Saul A., Novotny, Edward J., O’Brien, Terence J., Oliver, Karen L., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Park, Kristen L., Paterson, Sarah J., Petrovski, Slave, Pickrell, William O., Poduri, Annapurna, Rees, Mark I., Sadleir, Lynette G., Scheffer, Ingrid E., Shellhaas, Renee A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sirven, Joseph, Smith, Michael C., Smith, Philip E. M., Sperling, Michael R., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Vining, Eileen P. G., Von Allmen, Gretchen K., Weisenberg, Judith, Widdess‐Walsh, Peter, Winawer, Melodie R.

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