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Journal of Chemical Information and Modeling|January 28, 2015
Discovery of small molecule CD40-TRAF6 inhibitorsBarbara Zarzycka, Tom Seijkens, Sander B Nabuurs, et al.
Human Mutation|January 30, 2008
Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA bindingRob W J Collin, Ramesh Chellappa, Robert-Jan Pauw, et al.
Proteins|May 11, 2010
3DM: systematic analysis of heterogeneous superfamily data to discover protein functionalitiesRemko K Kuipers, Henk-Jan Joosten, Willem J H van Berkel, et al.
Physiological Genomics|August 13, 2009
Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 proteinHee Keun Lee, Mee Hyun Song, Myengmo Kang, et al.
Plos One|May 26, 2017
CorNet: Assigning function to networks of co-evolving residues by automated literature miningTom van den Bergh, Giorgio Tamo, Alberto Nobili, et al.
American Journal of Human Genetics|October 13, 2006
Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTsJan A M Smeitink, Orly Elpeleg, Hana Antonicka, et al.
Disease Models & Mechanisms|August 3, 2016
The role of the dopamine D1 receptor in social cognition: studies using a novel genetic rat modelJudith R Homberg, Jocelien D A Olivier, Marie VandenBroeke, et al.
European Journal of Human Genetics : EJHG|August 21, 2014
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraineSe-Kyung Oh, Jeong-In Baek, Karl M Weigand, et al.
Proteins|March 31, 2015
Key challenges for the creation and maintenance of specialist protein resourcesGemma L Holliday, Amos Bairoch, Pantelis G Bagos, et al.
Structure (London, England : 1993)|October 18, 2011
A new generation of crystallographic validation tools for the protein data bankRandy J Read, Paul D Adams, W Bryan Arendall, et al.
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