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

Por Petukh, Marharyta, Stefl, Shannon, Alexov, Emil
Publicado em 2013

Molecular mechanisms of disease-causing missense mutations

Por Stefl, Shannon, Nishi, Hafumi, Petukh, Marharyta, Panchenko, Anna R., Alexov, Emil
Publicado em 2013

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

Por Petukh, Marharyta, Wu, Bohua, Stefl, Shannon, Smith, Nick, Hyde-Volpe, David, Wang, Li, Alexov, Emil
Publicado no 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

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

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

Por 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
Publicado no Hum Mol Genet (2015)