Isolation and Functional Analysis of Human Neutrophils von Kuhns, Douglas B., Priel, Debra A. Long, Chu, Jessica, Zarember, Kol A.

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Chromothriptic Cure of WHIM Syndrome von McDermott, David H., Gao, Ji-Liang, Liu, Qian, Siwicki, Marie, Martens, Craig, Jacobs, Paejonette, Velez, Daniel, Yim, Erin, Bryke, Christine R., Hsu, Nancy, Dai, Zunyan, Marquesen, Martha M., Stregevsky, Elina, Kwatemaa, Nana, Theobald, Narda, Long Priel, Debra A., Pittaluga, Stefania, Raffeld, Mark A., Calvo, Katherine R., Maric, Irina, Desmond, Ronan, Holmes, Kevin L., Kuhns, Douglas B., Balabanian, Karl, Bachelerie, Françoise, Porcella, Stephen F., Malech, Harry L., Murphy, Philip M.

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Human PI3Kγ deficiency and its microbiota-dependent mouse model reveal immunodeficiency and tissue immunopathology von Takeda, Andrew J., Maher, Timothy J., Zhang, Yu, Lanahan, Stephen M., Bucklin, Molly L., Compton, Susan R., Tyler, Paul M., Comrie, William A., Matsuda, Makoto, Olivier, Kenneth N., Pittaluga, Stefania, McElwee, Joshua J., Long Priel, Debra A., Kuhns, Douglas B., Williams, Roger L., Mustillo, Peter J., Wymann, Matthias P., Koneti Rao, V., Lucas, Carrie L.

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Retrovirus gene therapy for X-linked chronic granulomatous disease can achieve stable long-term correction of oxidase activity in peripheral blood neutrophils von Kang, Elizabeth M., Choi, Uimook, Theobald, Narda, Linton, Gilda, Long Priel, Debra A., Kuhns, Doug, Malech, Harry L.

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Glycosylation, Hypogammaglobulinemia, and Resistance to Viral Infections von Sadat, Mohammed A, Moir, Susan, Chun, Tae-Wook, Lusso, Paolo, Kaplan, Gerardo, Wolfe, Lynne, Memoli, Matthew J, He, Miao, Vega, Hugo, Kim, Leo J.Y, Huang, Yan, Hussein, Nadia, Nievas, Elma, Mitchell, Raquel, Garofalo, Mary, Louie, Aaron, Ireland, Derek C, Grunes, Claire, Cimbro, Raffaello, Patel, Vyomesh, Holzapfel, Genevieve, Salahuddin, Daniel, Bristol, Tyler, Adams, David, Marciano, Beatriz E, Hegde, Madhuri, Li, Yuxing, Calvo, Katherine R, Stoddard, Jennifer, Justement, J. Shawn, Jacques, Jerome, Long Priel, Debra A, Murray, Danielle, Sun, Peter, Kuhns, Douglas B, Boerkoel, Cornelius F, Chiorini, John A, Di Pasquale, Giovanni, Verthelyi, Daniela, Rosenzweig, Sergio D

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The CXCR4 antagonist plerixafor corrects panleukopenia in patients with WHIM syndrome von McDermott, David H., Liu, Qian, Ulrick, Jean, Kwatemaa, Nana, Anaya-O'Brien, Sandra, Penzak, Scott R., Filho, Joao Oliveira, Priel, Debra A. Long, Kelly, Corin, Garofalo, Mary, Littel, Patricia, Marquesen, Martha M., Hilligoss, Diane, DeCastro, Rosamma, Fleisher, Thomas A., Kuhns, Douglas B., Malech, Harry L., Murphy, Philip M.

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X-linked Carriers of Chronic Granulomatous Disease: Illness, Lyonization and Stability von Marciano, Beatriz E., MD, Zerbe, Christa S., MD, Falcone, E. Liana, MD PhD, Ding, Li, MD, DeRavin, Suk See, MD PhD, Daub, Janine, CRNP, Kreuzburg, Samantha, CRNP, Yockey, Lynne, CRNP, Hunsberger, Sally, PHD, Foruraghi, Ladan, CRNP, Barnhart, Lisa A., CRNP, Matharu, Kabir, MD, Anderson, Victoria, CRNP, Darnell, Dirk N., CRNP, Frein, Cathleen, CRNP, Fink, Danielle L., MS, Lau, Karen P., MS, Long Priel, Debra A., MS, Gallin, John I., MD, Malech, Harry L., MD, Uzel, Gulbu, MD, Freeman, Alexandra F., MD, Kuhns, Douglas B., PhD, Rosenzweig, Sergio D., MD PhD, Holland, Steven M., MD

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A phase 1 clinical trial of long-term, low-dose treatment of WHIM syndrome with the CXCR4 antagonist plerixafor von McDermott, David H., Liu, Qian, Velez, Daniel, Lopez, Lizbeeth, Anaya-O'Brien, Sandra, Ulrick, Jean, Kwatemaa, Nana, Starling, Judy, Fleisher, Thomas A., Priel, Debra A. Long, Merideth, Melissa A., Giuntoli, Robert L., Evbuomwan, Moses O., Littel, Patricia, Marquesen, Martha M., Hilligoss, Dianne, DeCastro, Rosamma, Grimes, George J., Hwang, Samuel T., Pittaluga, Stefania, Calvo, Katherine R., Stratton, Pamela, Cowen, Edward W., Kuhns, Douglas B., Malech, Harry L., Murphy, Philip M.

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Severe congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis von McDermott, David H., De Ravin, Suk See, Jun, Hyun Sik, Liu, Qian, Priel, Debra A. Long, Noel, Pierre, Takemoto, Clifford M., Ojode, Teresa, Paul, Scott M., Dunsmore, Kimberly P., Hilligoss, Dianne, Marquesen, Martha, Ulrick, Jean, Kuhns, Douglas B., Chou, Janice Y., Malech, Harry L., Murphy, Philip M.

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Phase I Study of Zotiraciclib in Combination with Temozolomide for Patients with Recurrent High-grade Astrocytomas von Wu, Jing, Yuan, Ying, Long Priel, Debra A, Fink, Danielle, Peer, Cody J, Sissung, Tristan M, Su, Yu-Ting, Pang, Ying, Yu, Guangyang, Butler, Madison K, Mendoza, Tito R, Vera, Elizabeth, Ahmad, Salman, Bryla, Christine, Lindsley, Matthew, Grajkowska, Ewa, Mentges, Kelly, Boris, Lisa, Antony, Ramya, Garren, Nancy, Siegel, Christine, Lollo, Nicole, Cordova, Christine, Aboud, Orwa, Theeler, Brett J, Burton, Eric M, Penas-Prado, Marta, Leeper, Heather, Gonzales, Javier, Armstrong, Terri S, Calvo, Katherine R, Figg, William D, Kuhns, Douglas B, Gallin, John I, Gilbert, Mark R

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Assessment of Atherosclerosis in Chronic Granulomatous Disease von Sibley, Christopher T, Estwick, Tyra, Zavodni, Anna, Huang, Chiung-Yu, Kwan, Alan C, Soule, Benjamin P, Long Priel, Debra A, Remaley, Alan T, Rudman Spergel, Amanda K, Turkbey, Evrim B, Kuhns, Douglas B, Holland, Steven M, Malech, Harry L, Zarember, Kol A, Bluemke, David A, Gallin, John I

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Residual NADPH Oxidase and Survival in Chronic Granulomatous Disease von Kuhns, Douglas B, Alvord, W. Gregory, Heller, Theo, Feld, Jordan J, Pike, Kristen M, Marciano, Beatriz E, Uzel, Gulbu, DeRavin, Suk See, Priel, Debra A. Long, Soule, Benjamin P, Zarember, Kol A, Malech, Harry L, Holland, Steven M, Gallin, John I

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NCF1 (p47phox)–deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysis von Kuhns, Douglas B., Hsu, Amy P., Sun, David, Lau, Karen, Fink, Danielle, Griffith, Paul, Huang, Da Wei, Priel, Debra A. Long, Mendez, Laura, Kreuzburg, Samantha, Zerbe, Christa S., De Ravin, Suk See, Malech, Harry L., Holland, Steven M., Wu, Xiaolin, Gallin, John I.

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Induction of human monocyte interleukin (IL)-8 by fibrinogen through the toll-like receptor pathway von Kuhns, Douglas B, Priel, Debra A Long, Gallin, John I

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Loss-of-function of the protein kinase C δ (PKCδ) causes a B-cell lymphoproliferative syndrome in humans von Kuehn, Hye Sun, Niemela, Julie E., Rangel-Santos, Andreia, Zhang, Mingchang, Pittaluga, Stefania, Stoddard, Jennifer L., Hussey, Ashleigh A., Evbuomwan, Moses O., Priel, Debra A. Long, Kuhns, Douglas B., Park, C. Lucy, Fleisher, Thomas A., Uzel, Gulbu, Oliveira, João B.

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Signal transducer and activator of transcription 1 ( STAT1 ) gain-of-function mutations and disseminated coccidioidomycosis and histoplasmosis von Sampaio, Elizabeth P., MD, PhD, Hsu, Amy P., BA, Pechacek, Joseph, BA, Bax, Hannelore I., MD, Dias, Dalton L., BA, Paulson, Michelle L., MD, Chandrasekaran, Prabha, PhD, Rosen, Lindsey B., BS, Carvalho, Daniel S., PhD, Ding, Li, MD, Vinh, Donald C., MD, Browne, Sarah K., MD, Datta, Shrimati, PhD, Milner, Joshua D., MD, Kuhns, Douglas B., PhD, Long Priel, Debra A., BS, Sadat, Mohammed A., MD, Shiloh, Michael, MD, PhD, De Marco, Brendan, MD, Alvares, Michael, MD, Gillman, Jason W., MD, Ramarathnam, Vivek, MD, de la Morena, Maite, MD, Bezrodnik, Liliana, MD, Moreira, Ileana, MD, Uzel, Gulbu, MD, Johnson, Daniel, MD, Spalding, Christine, RN, Zerbe, Christa S., MD, Wiley, Henry, MD, Greenberg, David E., MD, Hoover, Susan E., MD, PhD, Rosenzweig, Sergio D., MD, PhD, Galgiani, John N., MD, Holland, Steven M., MD

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A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency von Zhou, Qing, Lee, Geun-Shik, Brady, Jillian, Datta, Shrimati, Katan, Matilda, Sheikh, Afzal, Martins, Marta S, Bunney, Tom D, Santich, Brian H, Moir, Susan, Kuhns, Douglas B, Long Priel, Debra A, Ombrello, Amanda, Stone, Deborah, Ombrello, Michael J, Khan, Javed, Milner, Joshua D, Kastner, Daniel L, Aksentijevich, Ivona

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Immunogenetics associated with severe coccidioidomycosis von Hsu, Amy P, Korzeniowska, Agnieszka, Aguilar, Cynthia C, Gu, Jingwen, Karlins, Eric, Oler, Andrew J, Chen, Gang, Reynoso, Glennys V, Davis, Joie, Chaput, Alexandria, Peng, Tao, Sun, Ling, Lack, Justin B, Bays, Derek J, Stewart, Ethan R, Waldman, Sarah E, Powell, Daniel A, Donovan, Fariba M, Desai, Jigar V, Pouladi, Nima, Long Priel, Debra A, Yamanaka, Daisuke, Rosenzweig, Sergio D, Niemela, Julie E, Stoddard, Jennifer, Freeman, Alexandra F, Zerbe, Christa S, Kuhns, Douglas B, Lussier, Yves A, Olivier, Kenneth N, Boucher, Richard C, Hickman, Heather D, Frelinger, Jeffrey, Fierer, Joshua, Shubitz, Lisa F, Leto, Thomas L, Thompson, 3rd, George R, Galgiani, John N, Lionakis, Michail S, Holland, Steven M

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Residual NADPH Oxidase and Survival in Chronic Granulomatous Disease von KUHNS, Douglas B, ALVORD, W. Gregory, ZAREMBER, Kol A, MALECH, Harry L, HOLLAND, Steven M, GALLIN, John I, HELLER, Theo, FELD, Jordan J, PIKE, Kristen M, MARCIANO, Beatriz E, UZEL, Gulbu, SUK SEE DERAVIN, LONG, Debra A, SOULE, Benjamin P

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Glycosylation, Hypogammaglobulinemia, and Resistance to Viral Infections von SADAT, Mohammed A, MOIR, Susan, YAN HUANG, HUSSEIN, Nadia, NIEVAS, Elma, MITCHELL, Raquel, GAROFALO, Mary, LOUIE, Aaron, IRELAND, Derek C, GRUNES, Claire, CIMBRO, Raffaello, PATEL, Vyomesh, CHUN, Tae-Wook, HOLZAPFEL, Genevieve, SALAHUDDIN, Daniel, BRISTOL, Tyler, ADAMS, David, MARCIANO, Beatriz E, HEGDE, Madhuri, YUXING LI, CALVO, Katherine R, STODDARD, Jennifer, JUSTEMENT, J. Shawn, LUSSO, Paolo, JACQUES, Jerome, PRIEL, Debra A. Long, MURRAY, Danielle, SUN, Peter, KUHNS, Douglas B, BOERKOEL, Cornelius F, CHIORINI, John A, DI PASQUALE, Giovanni, VERTHELYI, Daniela, ROSENZWEIG, Sergio D, KAPLAN, Gerardo, WOLFE, Lynne, MEMOLI, Matthew J, MIAO HE, VEGA, Hugo, KIM, Leo J. Y

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