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Journal of Chemical Information and Modeling|May 20, 2025
In Silico Screening for Small Molecules to Alter Calpain Proteolysis through Modulating Conformation Changes Induced by HeterodimerizationPitambar Poudel, Ivan Shapovalov, Shailesh Kumar Panday, et al.Plos One|June 27, 2013
Cancer missense mutations alter binding properties of proteins and their interaction networksHafumi Nishi, Manoj Tyagi, Shaolei Teng, et al.International Journal of Molecular Sciences|August 7, 2021
Computational Investigation of the pH Dependence of Stability of Melanosome Proteins: Implication for Melanosome formation and DiseaseMahesh Koirala, H B Mihiri Shashikala, Jacob Jeffries, et al.Journal of Alzheimer'S Disease : JAD|October 15, 2013
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 diseaseNatalia Dolzhanskaya, Michael A Gonzalez, Fiorella Sperziani, et al.BMC Biophysics|May 16, 2012
DelPhi: a comprehensive suite for DelPhi software and associated resourcesLin Li, Chuan Li, Subhra Sarkar, et al.The Journal of Physical Chemistry. B|February 14, 2006
Coating single-walled carbon nanotubes with phospholipidsYonnie Wu, JoAn S Hudson, Qi Lu, et al.Journal of Computational Chemistry|June 26, 2019
DelPhi Suite: New Developments and Review of FunctionalitiesChuan Li, Zhe Jia, Arghya Chakravorty, et al.Journal of Human Genetics|March 13, 2019
Three additional patients with EED-associated overgrowth: potential mutation hotspots identified?Catherine J Spellicy, Yunhui Peng, Leah Olewiler, et al.European Journal of Human Genetics : EJHG|January 24, 2018
Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defectsCatherine J Spellicy, Joy Norris, Renee Bend, et al.Human Molecular Genetics|July 21, 2012
An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activityKyoko Takano, Dan Liu, Patrick Tarpey, et al.Pageof 15