Drivers and relationship benefits of customer willingness to engage in CSR initiatives von O'Brien, Ingrid M, Ouschan, Robyn, Jarvis, Wade, Soutar, Geoffrey Norman

Volltext

Integrating social issues and customer engagement to drive loyalty in a service organisation von O'Brien, Ingrid M, Jarvis, Wade, Soutar, Geoffrey N

Volltext

Customer engagement in CSR: a utility theory model with moderating variables von Jarvis, Wade, Ouschan, Robyn, Burton, Henry J, Soutar, Geoffrey, O’Brien, Ingrid M

Volltext

Rethinking customer engagement design: Using customer-mobilized engagement (CME) to grow business networks von Davey, Janet, O'Brien, Ingrid, Ouschan, Robyn, Parkinson, Joy

Volltext

An Exploration of Dis-confirmation of Deeper Learning Expectations Using Choice Theory von Jarvis, Wade, Sadeque, Saalem, O’Brien, Ingrid Mary

Volltext

Co-creating a CSR Strategy with Customers to Deliver Greater Value von O’Brien, Ingrid M., Jarvis, Wade, Soutar, Geoffrey, Ouschan, Robyn

Volltext

Bilingual education for bilingual students von O’Brien, Ingrid

Volltext

Educating Emergent Bilinguals: Policies, Programs, and Practices for English Language Learners von O'Brien, Ingrid (Review of: Garcia, Ofelia, Kleifgen, Jo Anne)

Volltext

Mycobacterium tuberculosis Thioredoxin Reductase Is Essential for Thiol Redox Homeostasis but Plays a Minor Role in Antioxidant Defense von Lin, Kan, O'Brien, Kathryn M, Trujillo, Carolina, Wang, Ruojun, Wallach, Joshua B, Schnappinger, Dirk, Ehrt, Sabine

Volltext

Characterization of Human Engraftment and Hemophagocytic Lymphohistiocytosis in NSG-SGM3 Neonate Mice Engrafted with Purified CD34+ Hematopoietic Stem Cells von O'Brien, Liam J, Walpole, Carina M, Leal-Rojas, Ingrid M, Shatunova, Svetlana, Moore, Andrew, Winkler, Ingrid G, Guillerey, Camille, Radford, Kristen J

Volltext

The BRCA1-Δ11q Alternative Splice Isoform Bypasses Germline Mutations and Promotes Therapeutic Resistance to PARP Inhibition and Cisplatin von Wang, Yifan, Bernhardy, Andrea J, Cruz, Cristina, Krais, John J, Nacson, Joseph, Nicolas, Emmanuelle, Peri, Suraj, van der Gulden, Hanneke, van der Heijden, Ingrid, O'Brien, Shane W, Zhang, Yong, Harrell, Maribel I, Johnson, Shawn F, Candido Dos Reis, Francisco J, Pharoah, Paul D P, Karlan, Beth, Gourley, Charlie, Lambrechts, Diether, Chenevix-Trench, Georgia, Olsson, Håkan, Benitez, Javier J, Greene, Mark H, Gore, Martin, Nussbaum, Robert, Sadetzki, Siegal, Gayther, Simon A, Kjaer, Susanne K, D'Andrea, Alan D, Shapiro, Geoffrey I, Wiest, David L, Connolly, Denise C, Daly, Mary B, Swisher, Elizabeth M, Bouwman, Peter, Jonkers, Jos, Balmaña, Judith, Serra, Violeta, Johnson, Neil

Volltext

Ultra-rare genetic variation in common epilepsies: a case-control sequencing study von Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, 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, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

Volltext

Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue From Stereo-EEG Depth Electrodes von Ye, Zimeng, Bennett, Mark F., Neal, Andrew, Laing, Joshua A., Hunn, Martin K., Wittayacharoenpong, Thanomporn, Todaro, Marian, Patel, Sheila K., Bahlo, Melanie, Kwan, Patrick, O'Brien, Terence J., Scheffer, Ingrid E., Berkovic, Samuel F., Perucca, Piero, Hildebrand, Michael S.

Volltext

Human CD141+ dendritic cells (cDC1) are impaired in patients with advanced melanoma but can be targeted to enhance anti-PD-1 in a humanized mouse model von Lee, Yoke Seng, O'Brien, Liam J, Walpole, Carina M, Pearson, Frances E, Leal-Rojas, Ingrid M, Masterman, Kelly-Anne, Atkinson, Victoria, Barbour, Andrew, Radford, Kristen J

Volltext

Ferric citrate controls phosphorus and delivers iron in patients on dialysis von Lewis, Julia B, Sika, Mohammed, Koury, Mark J, Chuang, Peale, Schulman, Gerald, Smith, Mark T, Whittier, Frederick C, Linfert, Douglas R, Galphin, Claude M, Athreya, Balaji P, Nossuli, A Kaldun Kaldun, Chang, Ingrid J, Blumenthal, Samuel S, Manley, John, Zeig, Steven, Kant, Kotagal S, Olivero, Juan Jose, Greene, Tom, Dwyer, Jamie P

Volltext

De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies von Myers, Candace T., McMahon, Jacinta M., Schneider, Amy L., Petrovski, Slavé, Allen, Andrew S., Carvill, Gemma L., Zemel, Matthew, Saykally, Julia E., LaCroix, Amy J., Heinzen, Erin L., Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Johnson, Michael R., Kuzniecky, Ruben, Marson, Anthony G., O’Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Poduri, Annapurna, Pickrell, William O., Chung, Seo-Kyung, Rees, Mark I., Sherr, Elliott, Sadleir, Lynette G., Goldstein, David B., Lowenstein, Daniel H., Møller, Rikke S., Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

Volltext

REAL-WORLD UTILITY OF WHOLE EXOME SEQUENCING WITH TARGETED GENE ANALYSIS FOR FOCAL EPILEPSY von Perucca, Piero, Scheffer, Ingrid E, Harvey, A. Simon, James, Paul A, Lunke, Sebastian, Thorne, Natalie, Gaff, Clara, Regan, Brigid M, Damiano, John A, Hildebrand, Michael S, Berkovic, Samuel F, O’Brien, Terence J, Kwan, Patrick

Volltext

Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity von Meng, Bo, Abdullahi, Adam, Ferreira, Isabella A. T. M., Goonawardane, Niluka, Saito, Akatsuki, Kimura, Izumi, Yamasoba, Daichi, Gerber, Pehuén Pereyra, Fatihi, Saman, Rathore, Surabhi, Zepeda, Samantha K., Papa, Guido, Kemp, Steven A., Ikeda, Terumasa, Toyoda, Mako, Tan, Toong Seng, Kuramochi, Jin, Mitsunaga, Shigeki, Ueno, Takamasa, Shirakawa, Kotaro, Takaori-Kondo, Akifumi, Brevini, Teresa, Mallery, Donna L., Charles, Oscar J., Bowen, John E., Joshi, Anshu, Walls, Alexandra C., Jackson, Laurelle, Martin, Darren, Smith, Kenneth G. C., Bradley, John, Briggs, John A. G., Choi, Jinwook, Madissoon, Elo, Meyer, Kerstin B., Mlcochova, Petra, Ceron-Gutierrez, Lourdes, Doffinger, Rainer, Teichmann, Sarah A., Fisher, Andrew J., Pizzuto, Matteo S., de Marco, Anna, Corti, Davide, Hosmillo, Myra, Lee, Joo Hyeon, James, Leo C., Thukral, Lipi, Veesler, David, Sigal, Alex, Sampaziotis, Fotios, Goodfellow, Ian G., Matheson, Nicholas J., Sato, Kei, Gupta, Ravindra K.

Volltext

Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture von Harris, Rebekah V., Oliver, Karen L., Perucca, Piero, Striano, Pasquale, Labate, Angelo, Riva, Antonella, Grinton, Bronwyn E., Reid, Joshua, Hutton, Jessica, Todaro, Marian, O'Brien, Terence J., Kwan, Patrick, Sadleir, Lynette G., Mullen, Saul A., Dazzo, Emanuela, Crompton, Douglas E., Scheffer, Ingrid E., Bahlo, Melanie, Nobile, Carlo, Gambardella, Antonio, Berkovic, Samuel F.

Volltext

Mutations in DEPDC5 cause familial focal epilepsy with variable foci von Dibbens, Leanne M, de Vries, Boukje, Donatello, Simona, Heron, Sarah E, Hodgson, Bree L, Chintawar, Satyan, Crompton, Douglas E, Hughes, James N, Bellows, Susannah T, Klein, Karl Martin, Callenbach, Petra M C, Corbett, Mark A, Gardner, Alison E, Kivity, Sara, Iona, Xenia, Regan, Brigid M, Weller, Claudia M, Crimmins, Denis, O'Brien, Terence J, Guerrero-López, Rosa, Mulley, John C, Dubeau, Francois, Licchetta, Laura, Bisulli, Francesca, Cossette, Patrick, Thomas, Paul Q, Gecz, Jozef, Serratosa, Jose, Brouwer, Oebele F, Andermann, Frederick, Andermann, Eva, van den Maagdenberg, Arn M J M, Pandolfo, Massimo, Berkovic, Samuel F, Scheffer, Ingrid E

Volltext