X-linked lymphoproliferative syndromes: brothers or distant cousins?

Por Filipovich, Alexandra H., Zhang, Kejian, Snow, Andrew L., Marsh, Rebecca A.
Publicado em 2010

Next generation sequencing technologies in medical genetics

Por Valencia, C. Alexander., Pervaiz, M. Ali., Husami, Ammar., Qian, Yaping., Zhang, Kejian.
Publicado em 2013

Personalizing Drug Selection Using Advanced Clinical Decision Support

Por Pestian, John, Spencer, Malik, Matykiewicz, Pawel, Zhang, Kejian, Vinks, Sander, Glauser, Tracy
Publicado em 2009

Mediastinal small cell cancer associated with Lambert-Eaton myasthenic syndrome: A case report

Por ZHANG, KEJIAN, LIU, WEI, LI, YANG, ZHANG, KEWEI, GAO, XINLIANG, WANG, JING
Publicado no Exp Ther Med (2015)

LINC00210 plays oncogenic roles in non-small cell lung cancer by sponging microRNA-328-5p

Por Liu, Zhengjia, Xu, Lei, Zhang, Kejian, Guo, Bo, Cui, Zhi, Gao, Nan
Publicado no Exp Ther Med (2020)

Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation

Por Lindsley, Andrew W., Qian, Yaping, Valencia, C. Alexander, Shah, Kara, Zhang, Kejian, Assa’ad, Amal
Publicado no J Clin Immunol (2014)

Novel Mutation in Syntaxin-Binding Protein 2 (STXBP2) Prevents IL-2-induced Natural Killer Cell Cytotoxicity

Por Saltzman, Rushani W., Monaco-Shawver, Linda, Zhang, Kejian, Sullivan, Kathleen E., Filipovich, Alexandra H., Orange, Jordan S.
Publicado em 2012

Perforin and CD107a testing is superior to NK cell function testing for screening patients for genetic HLH

Por Rubin, Tamar S., Zhang, Kejian, Gifford, Carrie, Lane, Adam, Choo, Sharon, Bleesing, Jack J., Marsh, Rebecca A.
Publicado no Blood (2017)

Analysis of gene mutations in children with cholestasis of undefined etiology

Por Matte, Ursula, Mourya, Reena, Miethke, Alexander, Liu, Cong, Kauffmann, Gregory, Moyer, Katie, Zhang, Kejian, Bezerra, Jorge A.
Publicado em 2010

Genetics of pain perception, COMT and postoperative pain management in children

Por Sadhasivam, Senthilkumar, Chidambaran, Vidya, Olbrecht, Vanessa A, Esslinger, Hope R, Zhang, Kejian, Zhang, Xue, Martin, Lisa J
Publicado em 2014

Gene-expression signatures differ between different clinical forms of familial hemophagocytic lymphohistiocytosis

Por Sumegi, Janos, Nestheide, Shawnagay V., Barnes, Michael G., Villanueva, Joyce, Zhang, Kejian, Grom, Alexei A., Filipovich, Alexandra H.
Publicado em 2013

Novel UNC13D intronic variant disrupting a NFκB enhancer in a patient with recurrent macrophage activation syndrome and systemic juvenile idiopathic arthritis

Por Schulert, Grant S., Zhang, Mingce, Husami, Ammar, Fall, Ndate, Brunner, Hermine, Zhang, Kejian, Cron, Randy Q., Grom, Alexei A.
Publicado no Arthritis Rheumatol (2018)

Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosis

Por Zhang, Kejian, Chandrakasan, Shanmuganathan, Chapman, Heather, Valencia, C. Alexander, Husami, Ammar, Kissell, Diane, Johnson, Judith A., Filipovich, Alexandra H.
Publicado em 2014

Accuracy of flow cytometric perforin screening for detecting patients with FHL due to PRF1 mutations

Por Abdalgani, Manar, Filipovich, Alexandra H., Choo, Sharon, Zhang, Kejian, Gifford, Carrie, Villanueva, Joyce, Bleesing, Jack J., Marsh, Rebecca A.
Publicado no Blood (2015)

Frequency and spectrum of disease-causing variants in 1892 patients with suspected genetic HLH disorders

Por Gadoury-Levesque, Vanessa, Dong, Lei, Su, Rui, Chen, Jianjun, Zhang, Kejian, Risma, Kimberly A., Marsh, Rebecca A., Sun, Miao
Publicado no Blood Adv (2020)

Increased frequency of double and triple heterozygous gene variants in children with intrahepatic cholestasis

Por Goldschmidt, Monique L., Mourya, Reena, Connor, Jessica, Dexheimer, Phillip, Karns, Rebekah, Miethke, Alexander, Sheridan, Rachel, Zhang, Kejian, Bezerra, Jorge A.
Publicado no Hepatol Res (2015)

Elevated Granzyme B in Cytotoxic Lymphocytes is a Signature of Immune Activation in Hemophagocytic Lymphohistiocytosis

Por Mellor-Heineke, Sabine, Villanueva, Joyce, Jordan, Michael B., Marsh, Rebecca, Zhang, Kejian, Bleesing, Jack J., Filipovich, Alexandra H., Risma, Kimberly A.
Publicado em 2013

Hereditary xerocytosis: Diagnostic considerations

Por Risinger, Mary, Glogowska, Edyta, Chonat, Satheesh, Zhang, Kejian, Dagaonkar, Neha, Joiner, Clinton H., Quinn, Charles T., Kalfa, Theodosia A., Gallagher, Patrick G.
Publicado no Am J Hematol (2017)

Macrophage Activation Syndrome in Systemic Juvenile Idiopathic Arthritis is Associated With MUNC13-4 Gene Polymorphisms

Por Zhang, Kejian, Biroschak, Jennifer, Glass, David N., Thompson, Susan, Finkel, Terri, Passo, Murray H., Binstadt, Bryce A., Filipovich, Alexandra, Grom, Alexei A.
Publicado em 2008

Hemophagocytic lymphohistiocytosis caused by dominant-negative mutations in STXBP2 that inhibit SNARE-mediated membrane fusion

Por Spessott, Waldo A., Sanmillan, Maria L., McCormick, Margaret E., Patel, Nishant, Villanueva, Joyce, Zhang, Kejian, Nichols, Kim E., Giraudo, Claudio G.
Publicado no Blood (2015)