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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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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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 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 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 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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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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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 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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Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis von Onoufriadis, Alexandros, Simpson, Michael A., Pink, Andrew E., Di Meglio, Paola, Smith, Catherine H., Pullabhatla, Venu, Knight, Jo, Spain, Sarah L., Nestle, Frank O., Burden, A. David, Capon, Francesca, Trembath, Richard C., Barker, Jonathan N.

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Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH von Zhu, Na, Swietlik, Emilia M, Welch, Carrie L, Pauciulo, Michael W, Hagen, Jacob J, Zhou, Xueya, Guo, Yicheng, Karten, Johannes, Pandya, Divya, Tilly, Tobias, Lutz, Katie A, Martin, Jennifer M, Treacy, Carmen M, Rosenzweig, Erika B, Krishnan, Usha, Coleman, Anna W, Gonzaga-Jauregui, Claudia, Lawrie, Allan, Trembath, Richard C, Wilkins, Martin R, Morrell, Nicholas W, Shen, Yufeng, Gräf, Stefan, Nichols, William C, Chung, Wendy K

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A retrospective study of the impact of lifestyle on age at onset of Huntington disease von Trembath, M. Kaye, Horton, Zoë A., Tippett, Lynette, Hogg, Virginia, Collins, Veronica R., Churchyard, Andrew, Velakoulis, Dennis, Roxburgh, Richard, Delatycki, Martin B.

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Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease von Sharifi, Reza, Morra, Rosa, Denise Appel, C, Tallis, Michael, Chioza, Barry, Jankevicius, Gytis, Simpson, Michael A, Matic, Ivan, Ozkan, Ege, Golia, Barbara, Schellenberg, Matthew J, Weston, Ria, Williams, Jason G, Rossi, Marianna N, Galehdari, Hamid, Krahn, Juno, Wan, Alexander, Trembath, Richard C, Crosby, Andrew H, Ahel, Dragana, Hay, Ron, Ladurner, Andreas G, Timinszky, Gyula, Williams, R Scott, Ahel, Ivan

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Advection of surface-derived organic carbon fuels microbial reduction in Bangladesh groundwater von Mailloux, Brian J., Trembath-Reichert, Elizabeth, Cheung, Jennifer, Watson, Marlena, Stute, Martin, Freyer, Greg A., Ferguson, Andrew S., Ahmed, Kazi Matin, Alam, Md. Jahangir, Buchholz, Bruce A., Thomas, James, Layton, Alice C., Zheng, Yan, Bostick, Benjamin C., van Geen, Alexander

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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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Rare Pathogenic Variants in IL36RN Underlie a Spectrum of Psoriasis-Associated Pustular Phenotypes von Setta-Kaffetzi, Niovi, Navarini, Alexander A., Patel, Varsha M., Pullabhatla, Venu, Pink, Andrew E., Choon, Siew-Eng, Allen, Michael A., Burden, A David, Griffiths, Christopher E.M., Seyger, Marieke M.B., Kirby, Brian, Trembath, Richard C., Simpson, Michael A., Smith, Catherine H., Capon, Francesca, Barker, Jonathan N.

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