D003553Chemicals & DrugsD01.248.497.158.874.390.369D01.875.350.850.150.369D02.886.030.230.369D02.886.520.150.087D12.125.095.369D12.125.119.369D12.125.166.230.369110.998837Cystineprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns: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 ResourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonBiochemistryWake Forest School of MedicineGennadiyMoiseyevGennadiy P. Moiseyev PhD3178Moiseyev, GennadiyAssociate Professor12590612Moiseyev G, Crouch RK, Goletz P, Oatis J, Redmond TM, Ma JXBiochemistryMoiseyev G, Crouch RK, Goletz P, Oatis J, Redmond TM, Ma JX. Retinyl esters are the substrate for isomerohydrolase. Biochemistry. 2003 Feb 25; 42(7):2229-38.Biochemistry2003-02-25T00:00:002003Retinyl esters are the substrate for isomerohydrolase.true1Associate ProfessorAssociate Professor15546211Mohs AM, Wang X, Goodrich KC, Zong Y, Parker DL, Lu ZRBioconjugate chemistryMohs AM, Wang X, Goodrich KC, Zong Y, Parker DL, Lu ZR. PEG-g-poly(GdDTPA-co-L-cystine): a biodegradable macromolecular blood pool contrast agent for MR imaging. Bioconjug Chem. 2004 Nov-Dec; 15(6):1424-30.Bioconjug Chem2004-11-01T00:00:002004PEG-g-poly(GdDTPA-co-L-cystine): a biodegradable macromolecular blood pool contrast agent for MR imaging.16004476Mohs AM, Zong Y, Guo J, Parker DL, Lu ZRBiomacromoleculesMohs AM, Zong Y, Guo J, Parker DL, Lu ZR. PEG-g-poly(GdDTPA-co-L-cystine): effect of PEG chain length on in vivo contrast enhancement in MRI. Biomacromolecules. 2005 Jul-Aug; 6(4):2305-11.Biomacromolecules2005-07-01T00:00:002005PEG-g-poly(GdDTPA-co-L-cystine): effect of PEG chain length on in vivo contrast enhancement in MRI.17659618Mohs AM, Nguyen T, Jeong EK, Feng Y, Emerson L, Zong Y, Parker DL, Lu ZRMagnetic resonance in medicineMohs AM, Nguyen T, Jeong EK, Feng Y, Emerson L, Zong Y, Parker DL, Lu ZR. Modification of Gd-DTPA cystine copolymers with PEG-1000 optimizes pharmacokinetics and tissue retention for magnetic resonance angiography. Magn Reson Med. 2007 Jul; 58(1):110-8.Magn Reson Med2007-07-01T00:00:002007Modification of Gd-DTPA cystine copolymers with PEG-1000 optimizes pharmacokinetics and tissue retention for magnetic resonance angiography.0.2328210.2328211research area of0.2742580.07875254subject area for