C. Saraceni-Richards

发表

Text Mining Effectively Scores and Ranks the Literature for Improving Chemical-Gene-Disease Curation at the Comparative Toxicogenomics Database

Thomas C. Wiegers, Allan Peter Davis, Carolyn J. Mattingly, 2013, PloS one.

A conserved glutamate residue, Glu-257, is important for substrate binding and transport by the Escherichia coli mannitol permease

C. Saraceni-Richards, G. Jacobson, 1997, Journal of bacteriology.

Evidence for Interactions between Helices 5 and 8 and a Role for the Interdomain Loop in Tetracycline Resistance Mediated by Hybrid Tet Proteins*

Cynthia A. Saraceni-Richards, C. Saraceni-Richards, S. Levy, 2000, The Journal of Biological Chemistry.

Second-Site Suppressor Mutations of Inactivating Substitutions at Gly247 of the Tetracycline Efflux Protein, Tet(B)

C. Saraceni-Richards, S. Levy, 2000, Journal of bacteriology.

Tetracycline Efflux Protein , Tet ( B ) Inactivating Substitutions at Gly 247 of the Second-Site Suppressor Mutations of

C. Saraceni-Richards, S. Levy, 2000 .

Comparative Toxicogenomics Database: a knowledgebase and discovery tool for chemical–gene–disease networks

Thomas C. Wiegers, Allan Peter Davis, Carolyn J. Mattingly, 2008, Nucleic Acids Res..

The Comparative Toxicogenomics Database: update 2013

Thomas C. Wiegers, Allan Peter Davis, Carolyn J. Mattingly, 2012, Nucleic Acids Res..

The Comparative Toxicogenomics Database's 10th year anniversary: update 2015

Thomas C. Wiegers, Allan Peter Davis, Carolyn J. Mattingly, 2014, Nucleic Acids Res..

The Comparative Toxicogenomics Database: update 2011

Thomas C. Wiegers, Allan Peter Davis, Carolyn J. Mattingly, 2010, Nucleic Acids Res..

GeneComps and ChemComps: a new CTD metric to identify genes and chemicals with shared toxicogenomic profiles

Thomas C. Wiegers, Allan Peter Davis, Cynthia G. Murphy, 2009, Bioinformation.

TheEscherichia coli mannitol permease as a model for transport via the bacterial phosphotransferase system

C. Saraceni-Richards, G. Jacobson, 1993, Journal of bioenergetics and biomembranes.