D001555Chemicals & DrugsD02.455.426.559.389770.99662Benzene Derivativesprns:emailEncryptedemail addressprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:meshTreeNumberMeSH tree numberprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:positionInDepartmentposition in departmentprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierDepartmentvivo:hrJobTitleHR job titleInformation Resourcevivo:linkAnchorTextlink anchor textvivo:orcidIdORCID idPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forURLLinkvivo:webpagewebpagerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonMolecular Genetics and Cell BiologyMedicine-Infectious DiseasesNeurobiology30253098Jiang W, Thirman J, Jo S, Roux BThe journal of physical chemistry. BReduced Free Energy Perturbation/Hamiltonian Replica Exchange Molecular Dynamics Method with Unbiased Alchemical Thermodynamic Axis. J Phys Chem B. 2018 10 18; 122(41):9435-9442.J Phys Chem B2018-10-03T00:00:002018Reduced Free Energy Perturbation/Hamiltonian Replica Exchange Molecular Dynamics Method with Unbiased Alchemical Thermodynamic Axis.30711323Shields EP, Weber SGJournal of chromatography. AA liquid chromatographic charge transfer stationary phase based on the thiol-yne reaction. J Chromatogr A. 2019 Apr 26; 1591:1-6.J Chromatogr A2019-01-21T00:00:002019A liquid chromatographic charge transfer stationary phase based on the thiol-yne reaction.SunhwanJoSunhwan Jo0.000000000000000.000000000000003046Jo, SunhwanPost Doctoral ScholarChuanHe1Gp8Cq8dHMzMknJtY0fp/Cv/+94=Chuan He0.000000000000000.000000000000003123He, ChuanProfessor0.2516260.01333577research area of0.6837820.01870478subject area forhttp://voices.uchicago.edu/drsisodialab/Sisodia Labhttp://he-group.uchicago.eduMy Lab SiteBiochem/Mol BioChemistryUniversity of ChicagoJeanGreenberg3WV7DqQbG+n5hHlsaUXv9Gq0+s+oJean Greenberg41.78927490000000-87.601250000000001365Greenberg, Jean0000-0002-7213-7618ProfessorStephen G.WeberStephen G. Weber41.78927490000000-87.601250000000002476Weber, Stephen G.ProfessorSangram S.SisodiaxHF6ArIaHeX5hHlsaUXv9Gq0+s+oSangram S. Sisodia41.78927490000000-87.60125000000000510Sisodia, Sangram S.Professortrue1Post Doctoral ScholarPost Doctoral Scholartrue1ProfessorProfessortrue1ProfessorProfessortrue1ProfessorProfessortrue1ProfessorProfessor24380892Azam M, Islam MS, Al-Resayes SI, Rafiq Siddiqui M, Trzesowska-Kruszynska A, Kruszynski RSpectrochimica acta. Part A, Molecular and biomolecular spectroscopyPd(II) complexes based on quinoline derivative: structural characterization and their role as a catalyst for hydrogenation of (E)-1-methyl-4-(2-nitrovinyl)benzene. Spectrochim Acta A Mol Biomol Spectrosc. 2014 Apr 05; 123:1-6.Spectrochim Acta A Mol Biomol Spectrosc2013-12-12T00:00:002013Pd(II) complexes based on quinoline derivative: structural characterization and their role as a catalyst for hydrogenation of (E)-1-methyl-4-(2-nitrovinyl)benzene.24401146Wagner SL, Zhang C, Cheng S, Nguyen P, Zhang X, Rynearson KD, Wang R, Li Y, Sisodia SS, Mobley WC, Tanzi REBiochemistrySoluble ?-secretase modulators selectively inhibit the production of the 42-amino acid amyloid ß peptide variant and augment the production of multiple carboxy-truncated amyloid ß species. Biochemistry. 2014 Feb 04; 53(4):702-13.Biochemistry2014-01-22T00:00:002014Soluble ?-secretase modulators selectively inhibit the production of the 42-amino acid amyloid ß peptide variant and augment the production of multiple carboxy-truncated amyloid ß species.15137751Shi Z, He CJournal of the American Chemical SocietyAn Au-catalyzed cyclialkylation of electron-rich arenes with epoxides to prepare 3-chromanols. J Am Chem Soc. 2004 May 19; 126(19):5964-5.J Am Chem Soc2004-05-19T00:00:002004An Au-catalyzed cyclialkylation of electron-rich arenes with epoxides to prepare 3-chromanols.