Comèl-Netherton syndrome defined as primary immunodeficiency von Renner, Ellen D., MD, Hartl, Dominik, MD, Rylaarsdam, Stacey, AAS, Young, Marguerite L., BS, Monaco-Shawver, Linda, BA, Kleiner, Gary, MD, Markert, M. Louise, MD, Stiehm, E. Richard, MD, Belohradsky, Bernd H., MD, Upton, Melissa P., MD, Torgerson, Troy R., MD, PhD, Orange, Jordan S., MD, PhD, Ochs, Hans D., MD

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Substance P inhibits natural killer cell cytotoxicity through the neurokinin-1 receptor von Monaco‐Shawver, Linda, Schwartz, Lynnae, Tuluc, Florin, Guo, Chang‐Jiang, Lai, Jian Ping, Gunnam, Satya M., Kilpatrick, Laurie E., Banerjee, Pinaki P., Douglas, Steven D., Orange, Jordan S.

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Human immunodeficiency-causing mutation defines CD16 in spontaneous NK cell cytotoxicity von Grier, Jennifer T, Forbes, Lisa R, Monaco-Shawver, Linda, Oshinsky, Jennifer, Atkinson, T Prescott, Moody, Curtis, Pandey, Rahul, Campbell, Kerry S, Orange, Jordan S

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CD27 deficiency is associated with combined immunodeficiency and persistent symptomatic EBV viremia von van Montfrans, Joris M., MD, PhD, Hoepelman, Andy I.M., MD, PhD, Otto, Sigrid, BSc, van Gijn, Marielle, PhD, van de Corput, Lisette, PhD, de Weger, Roel A., PhD, Monaco-Shawver, Linda, BSc, Banerjee, Pinaki P., PhD, Sanders, Elisabeth A.M., MD, PhD, Jol–van der Zijde, Cornelia M., PhD, Betts, Michael R., PhD, Orange, Jordan S., MD, PhD, Bloem, Andries C., PhD, Tesselaar, Kiki, PhD

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Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder von Keller, Michael D., MD, Pandey, Rahul, PhD, Li, Dong, PhD, Glessner, Joseph, PhD, Tian, Lifeng, PhD, Henrickson, Sarah E., MD, PhD, Chinn, Ivan K., MD, Monaco-Shawver, Linda, BSc, Heimall, Jennifer, MD, Hou, Cuiping, BSc, Otieno, Frederick G., MS, Jyonouchi, Soma, MD, Calabrese, Leonard, DO, van Montfrans, Joris, MD, Orange, Jordan S., MD, PhD, Hakonarson, Hakon, MD, PhD

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Hypomorphic nuclear factor-κB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity von Hanson, Eric P., MD, Monaco-Shawver, Linda, BA, Solt, Laura A., BS, Madge, Lisa A., PhD, Banerjee, Pinaki P., PhD, May, Michael J., PhD, Orange, Jordan S., MD, PhD

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Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency von Mizesko, Melissa C., MD, Banerjee, Pinaki P., PhD, Monaco-Shawver, Linda, BA, Mace, Emily M., PhD, Bernal, William E., MD, Sawalle-Belohradsky, Julie, Belohradsky, Bernd H., MD, Heinz, Valerie, Freeman, Alexandra F., MD, Sullivan, Kathleen E., MD, PhD, Holland, Steven M., MD, Torgerson, Troy R., MD, PhD, Al-Herz, Waleed, MD, Chou, Janet, MD, Hanson, Imelda C., MD, Albert, Michael H., MD, Geha, Raif S., MD, Renner, Ellen D., MD, Orange, Jordan S., MD, PhD

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Recruitment of A20 by the C-terminal domain of NEMO suppresses NF-κB activation and autoinflammatory disease von Zilberman-Rudenko, Jevgenia, Shawver, Linda Monaco, Wessel, Alex W., Luo, Yongquan, Pelletier, Martin, Tsai, Wanxia Li, Lee, Younglang, Vonortas, Spiridon, Cheng, Laurence, Ashwell, Jonathan D., Orange, Jordan S., Siegel, Richard M., Hanson, Eric P.

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A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism von Netter, Petra, PhD, Chan, Sanny K., MD, PhD, Banerjee, Pinaki P., PhD, Monaco-Shawver, Linda, BS, Noroski, Lenora M., MD, MPH, Hanson, Imelda C., MD, Forbes, Lisa R., MD, Mace, Emily M., PhD, Chinen, Javier, MD, PhD, Gaspar, H. Bobby, PhD, Sleiman, Patrick, PhD, Hakonarson, Hakon, MD, PhD, Klein, Christoph, MD, PhD, Ehlayel, Mohammad S., MD, Orange, Jordan S., MD, PhD

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Differences in CD4IL-17+ in Children and Adults with Eosinophilic Esophagitis von Sindher, Sayantani B., MD, Monaco-Shawver, Linda, BS, Berry, Alexis, Spergel, Jonathan M., MD, PhD, FAAAAI, Cianferoni, Antonella, MD, PhD, FAAAAI

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Novel mutation in STXBP2 prevents IL-2–induced natural killer cell cytotoxicity von Saltzman, Rushani W., MD, Monaco-Shawver, Linda, BA, Zhang, Kejian, MD, MBA, Sullivan, Kathleen E., MD, PhD, Filipovich, Alexandra H., MD, Orange, Jordan S., MD, PhD

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Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset von Mace, Emily M, Hsu, Amy P, Monaco-Shawver, Linda, Makedonas, George, Rosen, Joshua B, Dropulic, Lesia, Cohen, Jeffrey I, Frenkel, Eugene P, Bagwell, John C, Sullivan, John L, Biron, Christine A, Spalding, Christine, Zerbe, Christa S, Uzel, Gulbu, Holland, Steven M, Orange, Jordan S

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Genome-wide analyses and functional profiling of human NK cell lines von Gunesch, Justin T., Angelo, Laura S., Mahapatra, Sanjana, Deering, Raquel P., Kowalko, Johanna E., Sleiman, Patrick, Tobias, John W., Monaco-Shawver, Linda, Orange, Jordan S., Mace, Emily M.

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Practical NK cell phenotyping and variability in healthy adults von Angelo, Laura S., Banerjee, Pinaki P., Monaco-Shawver, Linda, Rosen, Joshua B., Makedonas, George, Forbes, Lisa R., Mace, Emily M., Orange, Jordan S.

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Bilateral adrenal EBV-associated smooth muscle tumors in a child with a natural killer cell deficiency von Shaw, Rachel K., Issekutz, Andrew C., Fraser, Robert, Schmit, Pierre, Morash, Barb, Monaco-Shawver, Linda, Orange, Jordan S., Fernandez, Conrad V.

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Cdc42-interacting protein-4 functionally links actin and microtubule networks at the cytolytic NK cell immunological synapse von Banerjee, Pinaki P, Pandey, Rahul, Zheng, Rena, Suhoski, Megan M, Monaco-Shawver, Linda, Orange, Jordan S

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IL-2 induces a WAVE2-dependent pathway for actin reorganization that enables WASp-independent human NK cell function von Orange, Jordan S, Roy-Ghanta, Sumita, Mace, Emily M, Maru, Saumya, Rak, Gregory D, Sanborn, Keri B, Fasth, Anders, Saltzman, Rushani, Paisley, Allison, Monaco-Shawver, Linda, Banerjee, Pinaki P, Pandey, Rahul

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Novel Mutation in Syntaxin-Binding Protein 2 (STXBP2) Prevents IL-2-induced Natural Killer Cell Cytotoxicity von Saltzman, Rushani W., Monaco-Shawver, Linda, Zhang, Kejian, Sullivan, Kathleen E., Filipovich, Alexandra H., Orange, Jordan S.

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Novel mutation in STXBP2prevents IL-2―induced natural killer cell cytotoxicity von SALTZMAN, Rushani W, MONACO-SHAWVER, Linda, KEJIAN ZHANG, SULLIVAN, Kathleen E, FILIPOVICH, Alexandra H, ORANGE, Jordan S

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Human immunodeficiency-causing mutation defines CD16 in spontaneous NK cell cytotoxicity von Grier, Jennifer T, Forbes, Lisa R, Monaco-Shawver, Linda, Oshinsky, Jennifer, Atkinson, T. Prescott, Moody, Curtis, Pandey, Rahul, Campbell, Kerry S, Orange, Jordan S

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