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)

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

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

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)

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

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)

Drug-Metabolizing Enzyme Genotypes and Aggressive Behavior Treatment Response in Hospitalized Pediatric Psychiatric Patients

Por Prows, Cynthia A., Nick, Todd G., Saldaña, Shannon N., Pathak, Sanjeev, Liu, Chunyan, Zhang, Kejian, Daniels, Zachary S., Vinks, Alexander A., Glauser, Tracy A.
Publicado em 2009

Patients with X-Linked Lymphoproliferative Disease due to BIRC4 Mutation Have Normal Invariant Natural Killer T-Cell Populations

Por Marsh, Rebecca A., Villanueva, Joyce, Kim, Mi-Ok, Zhang, Kejian, Marmer, Dan, Risma, Kimberly A., Jordan, Michael B., Bleesing, Jack J., Filipovich, Alexandra H.
Publicado em 2009

XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease

Por Marsh, Rebecca A., Madden, Lisa, Kitchen, Brenda J., Mody, Rajen, McClimon, Brad, Jordan, Michael B., Bleesing, Jack J., Zhang, Kejian, Filipovich, Alexandra H.
Publicado em 2010

Gene expression profiling of peripheral blood mononuclear cells from children with active hemophagocytic lymphohistiocytosis

Por Sumegi, Janos, Barnes, Michael G., Nestheide, Shawnagay V., Molleran-Lee, Susan, Villanueva, Joyce, Zhang, Kejian, Risma, Kimberly A., Grom, Alexei A., Filipovich, Alexandra H.
Publicado em 2011

UGT1A9, UGT2B7 and MRP2 genotypes can predict mycophenolic acid pharmacokinetic variability in pediatric kidney transplant recipients

Por Fukuda, Tsuyoshi, Goebel, Jens, Cox, Shareen, Maseck, Denise, Zhang, Kejian, Sherbotie, Joseph R., Ellis, Eileen N., James, Laura P., Ward, Robert M., Vinks, Alexander A.
Publicado em 2012

Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy

Por Jodele, Sonata, Licht, Christoph, Goebel, Jens, Dixon, Bradley P., Zhang, Kejian, Sivakumaran, Theru A., Davies, Stella M., Pluthero, Fred G., Lu, Lily, Laskin, Benjamin L.
Publicado em 2013