More than Decoration: Roles for Natural Killer Group 2 Member D Ligand Expression by Immune Cells von Trembath, Andrew P, Markiewicz, Mary A

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Erratum. NKG2D Signaling Within the Pancreatic Islets Reduces NOD Diabetes and Increases Protective Central Memory CD8 + T-Cell Numbers. Diabetes 2020;69:1749–1762 von Trembath, Andrew P., Krausz, Kelsey L., Sharma, Neekun, Gerling, Ivan C., Mathews, Clayton E., Markiewicz, Mary A.

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NKG2D Signaling between Human NK Cells Enhances TACE-Mediated TNF-α Release von Sharma, Neekun, Trinidad, Camille V, Trembath, Andrew P, Markiewicz, Mary A

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NKG2D Signaling Within the Pancreatic Islets Reduces NOD Diabetes and Increases Protective Central Memory CD8 + T-Cell Numbers von Trembath, Andrew P, Krausz, Kelsey L, Sharma, Neekun, Gerling, Ivan C, Mathews, Clayton E, Markiewicz, Mary A

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A Protective Role for NKG2D-H60a Interaction via Homotypic T Cell Contact in Nonobese Diabetic Autoimmune Diabetes Pathogenesis von Trembath, Andrew P, Sharma, Neekun, Raju, Saravanan, Polić, Bojan, Markiewicz, Mary A

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NKG2D signaling within the pancreas enhances CD8+ central memory T cell formation and decreases non-obese diabetic (NOD) diabetes development von Trembath, Andrew P., Sharma, Neekun, Markiewicz, Mary A.

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NKG2D signaling within the pancreas decreases NOD diabetes by enhancing CD8+ central memory T cell formation von Markiewicz, Mary A, Trembath, Andrew P, Sharma, Neekun, Mathews, Clayton E

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NKG2D signaling between human NK cells enhances TACE-mediated TNF-α release1 von Sharma, Neekun, Trinidad, Camille V., Trembath, Andrew P., Markiewicz, Mary A.

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Abstract 4841: Suppression of metastasis by KP54 and non-KP54 kisspeptins von Hampton, Kelsey Rebecca, Pounds, Keke M., Trembath, Andrew P., Welch, Danny R.

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Abstract 1615: Metastasis suppression by KP54 and non-KP54 kisspeptins von Hampton, Kelsey R., Pounds, Keke M., Trembath, Andrew P., Welch, Danny R.

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NKG2D-H60a interaction via homotypic T cell contact delays NOD diabetes development von Trembath, Andrew P, Sharma, Neekun, Matocha, Kimberly Nicole, Markiewicz, Mary A

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Genetic correlations among psychiatric and immune‐related phenotypes based on genome‐wide association data von Tylee, Daniel S., Sun, Jiayin, Hess, Jonathan L., Tahir, Muhammad A., Sharma, Esha, Malik, Rainer, Worrall, Bradford B., Levine, Andrew J., Martinson, Jeremy J., Nejentsev, Sergey, Speed, Doug, Fischer, Annegret, Mick, Eric, Walker, Brian R., Crawford, Andrew, Grant, Struan F. A., Polychronakos, Constantin, Bradfield, Jonathan P., Sleiman, Patrick M. A., Hakonarson, Hakon, Ellinghaus, Eva, Elder, James T., Tsoi, Lam C., Trembath, Richard C., Barker, Jonathan N., Franke, Andre, Dehghan, Abbas, Faraone, Stephen V., Glatt, Stephen J.

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Aberrant Expression and Subcellular Localization of ECT2 Drives Colorectal Cancer Progression and Growth von Cook, Danielle R, Kang, Melissa, Martin, Timothy D, Galanko, Joseph A, Loeza, Gabriela H, Trembath, Dimitri G, Justilien, Verline, Pickering, Karen A, Vincent, David F, Jarosch, Armin, Jurmeister, Philipp, Waters, Andrew M, Hibshman, Priya S, Campbell, Andrew D, Ford, Catriona A, Keku, Temitope O, Yeh, Jen Jen, Lee, Michael S, Cox, Adrienne D, Fields, Alan P, Sandler, Robert S, Sansom, Owen J, Sers, Christine, Schaefer, Antje, Der, Channing J

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Defining the clinical validity of genes reported to cause pulmonary arterial hypertension von Welch, Carrie L., Aldred, Micheala A., Balachandar, Srimmitha, Dooijes, Dennis, Eichstaedt, Christina A., Gräf, Stefan, Houweling, Arjan C., Machado, Rajiv D., Pandya, Divya, Prapa, Matina, Shaukat, Memoona, Southgate, Laura, Tenorio-Castano, Jair, Callejo, Emily P., Day, Kristina M., Macaya, Daniela, Maldonado-Velez, Gabriel, Chung, Wendy K., Archer, Stephen L., Auckland, Kathryn, Austin, Eric D., Badagliacca, Roberto, Barberà, Joan-Albert, Belge, Catharina, Bogaard, Harm Jan, Bonnet, Sébastien, Boomars, Karin A., Boucherat, Olivier, Chakinala, Murali M., Condliffe, Robin, Damico, Rachel Lynn, Delcroix, Marion, Desai, Ankit A., Doboszynska, Anna, Elliott, C. Greg, Eyries, Melanie, Escribano Subías, Maria Pilar, Gall, Henning, Ghio, Stefano, Ghofrani, Ardeschir-Hossein, Grünig, Ekkehard, Hamid, Rizwan, Harbaum, Lars, Hassoun, Paul M., Hemnes, Anna R., Hinderhofer, Katrin, Howard, Luke S., Humbert, Marc, Kiely, David G., Langleben, David, Lawrie, Allan, Loyd, Jim E., Moledina, Shahin, Montani, David, Morrell, Nichols W., Nichols, William C., Olschewski, Andrea, Olschewski, Horst, Papa, Silvia, Pauciulo, Mike W., Provencher, Steve, Quarck, Rozenn, Rhodes, Christopher J., Scelsi, Laura, Seeger, Werner, Stewart, Duncan J., Sweatt, Andrew, Swietlik, Emilia M., Treacy, Carmen, Trembath, Richard C., Tura-Ceide, Olga, Vizza, Carmine Dario, Vonk Noordegraaf, Anton, Wilkins, Martin R., Zamanian, Roham T., Zateyshchikov, Dmitry

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Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes von Zhou, Kaixin, Bellenguez, Celine, Spencer, Chris C A, Bennett, Amanda J, Coleman, Ruth L, Tavendale, Roger, Hawley, Simon A, Donnelly, Louise A, Schofield, Chris, Groves, Christopher J, Burch, Lindsay, Carr, Fiona, Strange, Amy, Freeman, Colin, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Duncanson, Audrey, Edkins, Sarah, Gray, Emma, Hunt, Sarah, Jankowski, Janusz, Langford, Cordelia, Markus, Hugh S, Mathew, Christopher G, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Samani, Nilesh J, Trembath, Richard, Viswanathan, Ananth C, Wood, Nicholas W, Harries, Lorna W, Hattersley, Andrew T, Doney, Alex S F, Colhoun, Helen, Morris, Andrew D, Sutherland, Calum, Hardie, D Grahame, Peltonen, Leena, McCarthy, Mark I, Holman, Rury R, Palmer, Colin N A, Donnelly, Peter, Pearson, Ewan R

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Mutations in VPS33B , encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome von Stapelbroek, Janneke M, Morgan, Neil V, Johnson, Colin A, Lo, Bryan, Karet, Fiona E, McKiernan, Patrick J, Knisely, A S, Forshew, Tim, Morris, Andrew A M, Trembath, Richard C, Houwen, Roderick H J, Wraith, James E, Quarrell, Oliver W, Cooper, Wendy N, Maher, Eamonn R, Klomp, Leo W J, Thompson, Richard J, Wali, S, Gissen, Paul, Kelly, Deirdre A, McClean, Patricia, Di Rocco, Maja, Mandel, Hanna, Lynch, Sally A

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Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-β family von Thomson, Jennifer R, Machado, Rajiv D, Pauciulo, Michael W, Morgan, Neil V, Humbert, Marc, Elliott, Greg C, Ward, Ken, Yacoub, Magdi, Mikhail, Ghada, Rogers, Paula, Newman, John, Wheeler, Lisa, Higenbottam, Timothy, Gibbs, J Simon R, Egan, Jim, Crozier, Agnes, Peacock, Andrew, Allcock, Robert, Corris, Paul, Loyd, James E, Trembath, Richard C, Nichols, William C

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Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension von Hadinnapola, Charaka, Bleda, Marta, Haimel, Matthias, Screaton, Nicholas, Swift, Andrew, Dorfmüller, Peter, Preston, Stephen D, Southwood, Mark, Hernandez-Sanchez, Jules, Martin, Jennifer, Treacy, Carmen, Yates, Katherine, Bogaard, Harm, Church, Colin, Coghlan, Gerry, Condliffe, Robin, Corris, Paul A, Gibbs, Simon, Girerd, Barbara, Holden, Simon, Humbert, Marc, Kiely, David G, Lawrie, Allan, Machado, Rajiv, MacKenzie Ross, Robert, Moledina, Shahin, Montani, David, Newnham, Michael, Peacock, Andrew, Pepke-Zaba, Joanna, Rayner-Matthews, Paula, Shamardina, Olga, Soubrier, Florent, Southgate, Laura, Suntharalingam, Jay, Toshner, Mark, Trembath, Richard, Vonk Noordegraaf, Anton, Wilkins, Martin R, Wort, Stephen J, Wharton, John, Gräf, Stefan, Morrell, Nicholas W

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Common genetic determinants of intraocular pressure and primary open-angle glaucoma von van Koolwijk, Leonieke M E, Ramdas, Wishal D, Ikram, M Kamran, Jansonius, Nomdo M, Pasutto, Francesca, Hysi, Pirro G, Macgregor, Stuart, Janssen, Sarah F, Hewitt, Alex W, Viswanathan, Ananth C, ten Brink, Jacoline B, Hosseini, S Mohsen, Amin, Najaf, Despriet, Dominiek D G, Willemse-Assink, Jacqueline J M, Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S, Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y, Gramer, Eugen, Welge-Lüssen, Ulrich, Montgomery, Grant W, Carbonaro, Francis, Young, Terri L, Bellenguez, Céline, McGuffin, Peter, Foster, Paul J, Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y, Czudowska, Monika A, Hofman, Albert, Uitterlinden, Andre G, Wolfs, Roger C W, de Jong, Paulus T V M, Oostra, Ben A, Paterson, Andrew D, Mackey, David A, Bergen, Arthur A B, Reis, André, Hammond, Christopher J, Vingerling, Johannes R, Lemij, Hans G, Klaver, Caroline C W, van Duijn, Cornelia M

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Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus von Raymond, F Lucy, Gottlob, Irene, Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, Asproudis, Ioannis, Zubcov, Alina A, Pieh, Christina, Veal, Colin D, Machado, Rajiv D, Backhouse, Oliver C, Baumber, Laura, Constantinescu, Cris S, Brodsky, Michael C, Hunter, David G, Hertle, Richard W, Read, Randy J, Edkins, Sarah, O'Meara, Sarah, Parker, Adrian, Stevens, Claire, Teague, Jon, Wooster, Richard, Futreal, P Andrew, Trembath, Richard C, Stratton, Michael R

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