The Role of Protonation States in Ligand-Receptor Recognition and Binding

per Petukh, Marharyta, Stefl, Shannon, Alexov, Emil
Publicat 2013

Molecular mechanisms of disease-causing missense mutations

per Stefl, Shannon, Nishi, Hafumi, Petukh, Marharyta, Panchenko, Anna R., Alexov, Emil
Publicat 2013

Chronic Beryllium Disease: Revealing the Role of Beryllium Ion and Small Peptides Binding to HLA-DP2

per Petukh, Marharyta, Wu, Bohua, Stefl, Shannon, Smith, Nick, Hyde-Volpe, David, Wang, Li, Alexov, Emil
Publicat a PLoS One (2014)

A novel p.Leu(381)Phe mutation in Presenilin 1 is associated with very early onset and unusually fast progressing dementia, and lysosomal inclusions typically seen in Kufs disease

per Dolzhanskaya, Natalia, Gonzalez, Michael A., Sperziani, Fiorella, Stefl, Shannon, Messing, Jeffrey, Wen, Guang Y, Alexov, Emil, Stephan Zuchner, S, Velinov, Milen
Publicat 2014

ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons

per May, Melanie, Hwang, Kyu-Seok, Miles, Judith, Williams, Charlie, Niranjan, Tejasvi, Kahler, Stephen G., Chiurazzi, Pietro, Steindl, Katharina, Van Der Spek, Peter J., Swagemakers, Sigrid, Mueller, Jennifer, Stefl, Shannon, Alexov, Emil, Ryu, Jeong-Im, Choi, Jung-Hwa, Kim, Hyun-Taek, Tarpey, Patrick, Neri, Giovanni, Holloway, Lynda, Skinner, Cindy, Stevenson, Roger E., Dorsky, Richard I., Wang, Tao, Schwartz, Charles E., Kim, Cheol-Hee
Publicat a Hum Mol Genet (2015)