Aurora B Interacts with NIR-p53, Leading to p53 Phosphorylation in Its DNA-binding Domain and Subsequent Functional Suppression

av Wu, Liming, Ma, Chi A., Zhao, Yongge, Jain, Ashish
Publicerad 2011

Impaired dendritic-cell function in ectodermal dysplasia with immune deficiency is linked to defective NEMO ubiquitination

av Temmerman, Stephane T., Ma, Chi A., Borges, Louis, Kubin, Marek, Liu, Shuying, Derry, Jonathan M. J., Jain, Ashish
Publicerad 2006

Impaired regulation of NF-κB and increased susceptibility to colitis-associated tumorigenesis in CYLD-deficient mice

av Zhang, Jun, Stirling, Brigid, Temmerman, Stephane T., Ma, Chi A., Fuss, Ivan J., Derry, Jonathan M.J., Jain, Ashish
Publicerad 2006

Dendritic cells from humans with hypomorphic mutations in NEMO have impaired mitogen-activated protein kinase activity

av Ma, Chi A., Wang, Hong-Ying, Temmerman, Stephane, Zhao, Yongge, Wu, Liming, Hornung, Ronald L., Wara, Diane, Jain, Ashish
Publicerad 2011

Novel INHAT Repressor (NIR) is required for early lymphocyte development

av Ma, Chi A., Pusso, Antonia, Wu, Liming, Zhao, Yongge, Hoffmann, Victoria, Notarangelo, Luigi D., Fowlkes, B. J., Jain, Ashish
Publicerad 2014

CYLD and the NEMO Zinc Finger Regulate Tumor Necrosis Factor Signaling and Early Embryogenesis

av Zhao, Yongge, Ma, Chi A., Wu, Liming, Iwai, Kazuhiro, Ashwell, Jonathan D., Oltz, Eugene M., Ballard, Dean W., Jain, Ashish
I publikationen J Biol Chem (2015)

Specific NEMO mutations impair CD40-mediated c-Rel activation and B cell terminal differentiation

av Jain, Ashish, Ma, Chi A., Lopez-Granados, Eduardo, Means, Gary, Brady, William, Orange, Jordan S., Liu, Shuying, Holland, Steven, Derry, Jonathan M.J.
Publicerad 2004

The Deubiquitinase CYLD Targets Smad7 Protein to Regulate Transforming Growth Factor β (TGF-β) Signaling and the Development of Regulatory T Cells

av Zhao, Yongge, Thornton, Angela M., Kinney, Matthew C., Ma, Chi A., Spinner, Jacob J., Fuss, Ivan J., Shevach, Ethan M., Jain, Ashish
Publicerad 2011

Defective nuclear IKKα function in patients with ectodermal dysplasia with immune deficiency

av Temmerman, Stephane T., Ma, Chi A., Zhao, Yongge, Keenan, Jeffrey, Aksentijevich, Ivona, Fessler, Margaret, Brown, Margaret R., Knutsen, Alan, Shapiro, Ralph, Jain, Ashish
Publicerad 2011

A Novel Mutation in NFKBIA/IKBA Results in a Degradation-Resistant N-Truncated Protein and Is Associated With Ectodermal Dysplasia With Immunodeficiency

av Lopez-Granados, Eduardo, Keenan, Jeffrey E., Kinney, Matthew C., Leo, Harvey, Jain, Neal, Ma, Chi A., Quinones, Ralph, Gelfand, Erwin W., Jain, Ashish
Publicerad 2008

Antibody deficiency associated with an inherited autosomal dominant mutation in TWEAK

av Wang, Hong-Ying, Ma, Chi A., Zhao, Yongge, Fan, Xiying, Zhou, Qing, Edmonds, Pamela, Uzel, Gulbu, Oliveira, Joao Bosco, Orange, Jordan, Jain, Ashish
Publicerad 2013

PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients

av Zhang, Yuan, Ma, Chi A., Lawrence, Monica G., Break, Timothy J., O’Connell, Michael P., Lyons, Jonathan J., López, Diego B., Barber, John S., Zhao, Yongge, Barber, Daniel L., Freeman, Alexandra F., Holland, Steven M., Lionakis, Michail S., Milner, Joshua D.
I publikationen J Exp Med (2017)

CD40 agonist antibody mediated improvement of chronic Cryptosporidium infection in patients with X- linked hyper IgM syndrome

av Fan, Xiying, Upadhyaya, Bhaskar, Wu, Liming, Koh, Christopher, Santín-Durán, Mónica, Pittaluga, Stefania, Uzel, Gulbu, Kleiner, David, Williams, Ester, Ma, Chi A., Bodansky, Aaron, Oliveira, Joao B., Edmonds, Pamela, Hornung, Ronald, Wong, Duane W., Fayer, Ronald, Fleisher, Tom, Heller, Theo, Prussin, Calman, Jain, Ashish
Publicerad 2012

Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrhea

av Ma, Chi A., Xi, Liqiang, Cauff, Brian, DeZure, Adam, Freeman, Alexandra F., Hambleton, Sophie, Kleiner, Gary, Leahy, T. Ronan, O’Sullivan, Maureen, Makiya, Michelle, O’Regan, Grainne, Pittaluga, Stefania, Niemela, Julie, Stoddard, Jennifer, Rosenzweig, Sergio D., Raffeld, Mark, Klion, Amy D., Milner, Joshua D.
I publikationen Blood (2017)

Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects

av Lev, Atar, Lee, Yu Nee, Sun, Guangping, Hallumi, Enas, Simon, Amos J., Zrihen, Keren S., Levy, Shiran, Beit Halevi, Tal, Papazian, Maria, Shwartz, Neta, Somekh, Ido, Levy-Mendelovich, Sarina, Wolach, Baruch, Gavrieli, Ronit, Vernitsky, Helly, Barel, Ortal, Javasky, Elisheva, Stauber, Tali, Ma, Chi A., Zhang, Yuan, Amariglio, Ninette, Rechavi, Gideon, Hendel, Ayal, Yablonski, Deborah, Milner, Joshua D., Somech, Raz
I publikationen J Exp Med (2020)

Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responses

av Spencer, Sarah, Köstel Bal, Sevgi, Egner, William, Lango Allen, Hana, Raza, Syed I., Ma, Chi A., Gürel, Meltem, Zhang, Yuan, Sun, Guangping, Sabroe, Ruth A., Greene, Daniel, Rae, William, Shahin, Tala, Kania, Katarzyna, Ardy, Rico Chandra, Thian, Marini, Staples, Emily, Pecchia-Bekkum, Annika, Worrall, William P.M., Stephens, Jonathan, Brown, Matthew, Tuna, Salih, York, Melanie, Shackley, Fiona, Kerrin, Diarmuid, Sargur, Ravishankar, Condliffe, Alison, Tipu, Hamid Nawaz, Kuehn, Hye Sun, Rosenzweig, Sergio D., Turro, Ernest, Tavaré, Simon, Thrasher, Adrian J., Jodrell, Duncan Ian, Smith, Kenneth G.C., Boztug, Kaan, Milner, Joshua D., Thaventhiran, James E.D.
I publikationen J Exp Med (2019)

Germline hypomorphic CARD11 mutations in severe atopic disease

av Ma, Chi A, Stinson, Jeffrey R, Zhang, Yuan, Abbott, Jordan K, Weinreich, Michael A, Hauk, Pia J, Reynolds, Paul R, Lyons, Jonathan J, Nelson, Celeste G, Ruffo, Elisa, Dorjbal, Batsukh, Glauzy, Salomé, Yamakawa, Natsuko, Arjunaraja, Swadhinya, Voss, Kelsey, Stoddard, Jennifer, Niemela, Julie, Zhang, Yu, Rosenzweig, Sergio D, McElwee, Joshua J, DiMaggio, Thomas, Matthews, Helen F, Jones, Nina, Stone, Kelly D, Palma, Alejandro, Oleastro, Matías, Prieto, Emma, Bernasconi, Andrea R, Dubra, Geronimo, Danielian, Silvia, Zaiat, Jonathan, Marti, Marcelo A, Kim, Brian, Cooper, Megan A, Romberg, Neil D, Meffre, Eric, Gelfand, Erwin W, Snow, Andrew L, Milner, Joshua D
I publikationen Nat Genet (2017)

Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations

av Milner, Joshua D., Vogel, Tiphanie P., Forbes, Lisa, Ma, Chi A., Stray-Pedersen, Asbjørg, Niemela, Julie E., Lyons, Jonathan J., Engelhardt, Karin R., Zhang, Yu, Topcagic, Nermina, Roberson, Elisha D. O., Matthews, Helen, Verbsky, James W., Dasu, Trivikram, Vargas-Hernandez, Alexander, Varghese, Nidhy, McClain, Kenneth L., Karam, Lina B., Nahmod, Karen, Makedonas, George, Mace, Emily M., Sorte, Hanne S., Perminow, Gøri, Rao, V. Koneti, O’Connell, Michael P., Price, Susan, Su, Helen C., Butrick, Morgan, McElwee, Joshua, Hughes, Jason D., Willet, Joseph, Swan, David, Xu, Yaobo, Santibanez-Koref, Mauro, Slowik, Voytek, Dinwiddie, Darrell L., Ciaccio, Christina E., Saunders, Carol J., Septer, Seth, Kingsmore, Stephen F., White, Andrew J., Cant, Andrew J., Hambleton, Sophie, Cooper, Megan A.
I publikationen Blood (2015)

Hypomorphic CARD11 mutations associated with diverse immunologic phenotypes with or without atopic disease.

av Dorjbal, Batsukh, Stinson, Jeffrey R., Ma, Chi A., Weinreich, Michael A., Miraghazadeh, Bahar, Hartberger, Julia M., Frey-Jakobs, Stefanie, Weidinger, Stephan, Moebus, Lena, Franke, Andre, Schäffer, Alejandro A., Bulashevska, Alla, Fuchs, Sebastian, Ehl, Stephan, Limaye, Sandhya, Arkwright, Peter D., Briggs, Tracy A., Langley, Claire, Bethune, Claire, Whyte, Andrew F., Alachkar, Hana, Nejentsev, Sergey, DiMaggio, Thomas, Nelson, Celeste G., Stone, Kelly D., Nason, Martha, Brittain, Erica H., Oler, Andrew J., Veltri, Daniel P., Leahy, T. Ronan, Conlon, Niall, Poli, Maria C., Borzutzky, Arturo, Cohen, Jeffrey I., Davis, Joie, Lambert, Michele P., Romberg, Neil, Sullivan, Kathleen E., Paris, Kenneth, Freeman, Alexandra F., Lucas, Laura, Chandrakasan, Shanmuganathan, Savic, Sinisa, Hambleton, Sophie, Patel, Smita Y, Jordan, Michael B., Theos, Amy, Lebensburger, Jeffrey, Atkinson, T. Prescott, Torgerson, Troy R., Chinn, Ivan K., Milner, Joshua D., Grimbacher, Bodo, Cook, Matthew C., Snow, Andrew L.
I publikationen J Allergy Clin Immunol (2018)