Publications by authors named "Shannon Stefl"

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ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons.
Melanie May, Kyu-Seok Hwang, Judith Miles, Charlie Williams, Tejasvi Niranjan, Shannon Stefl

Hum Mol Genet· September 2015

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Chronic Beryllium Disease: revealing the role of beryllium ion and small peptides binding to HLA-DP2.
Marharyta Petukh, Bohua Wu, Shannon Stefl, Nick Smith, David Hyde-Volpe

PLoS One· June 2015

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A novel p.Leu(381)Phe mutation in presenilin 1 is associated with very early onset and unusually fast progressing dementia as well as lysosomal inclusions typically seen in Kufs disease.
Natalia Dolzhanskaya, Michael A Gonzalez, Fiorella Sperziani, Shannon Stefl, Jeffrey Messing

J Alzheimers Dis· September 2014

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The role of protonation states in ligand-receptor recognition and binding.
Marharyta Petukh, Shannon Stefl, Emil Alexov

Curr Pharm Des· December 2013

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Molecular mechanisms of disease-causing missense mutations.
Shannon Stefl, Hafumi Nishi, Marharyta Petukh, Anna R Panchenko, Emil Alexov

J Mol Biol· November 2013

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