D003412Living BeingsB01.050.150.900.649.313.992.635.075.250.250651260.976802Cricetulusprns: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 textPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forURLLinkvivo:webpagewebpagerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson0.4561180.0038629965research area of0.230760.0116476139subject area for32810216Déri S, Borbás J, Hartai T, Hategan L, Csányi B, Visnyovszki Á, Madácsy T, Maléth J, Hegedus Z, Nagy I, Arora R, Labro AJ, Környei L, Varró A, Sepp R, Ördög BCardiovascular researchImpaired cytoplasmic domain interactions cause co-assembly defect and loss of function in the p.Glu293Lys KNCJ2 variant isolated from an Andersen-Tawil syndrome patient. Cardiovasc Res. 2021 07 07; 117(8):1923-1934.Cardiovasc Res2021-07-07T00:00:002021Impaired cytoplasmic domain interactions cause co-assembly defect and loss of function in the p.Glu293Lys KNCJ2 variant isolated from an Andersen-Tawil syndrome patient.Radiation & Cellular OncologyComm: NeurobiologySteveGoldsteinSteve A.n. Goldstein0.000000000000000.000000000000003032Goldstein, StevePROFESSOR Ben May Department of Cancer Research34090922Gallo E, Kelil A, Haughey M, Cazares-Olivera M, Yates BP, Zhang M, Wang NY, Blazer L, Carderelli L, Adams JJ, Kossiakoff AA, Wells JA, Xie W, Sidhu SSJournal of molecular biologyInhibition of Cancer Cell Adhesion, Migration and Proliferation by a Bispecific Antibody that Targets two Distinct Epitopes on av Integrins. J Mol Biol. 2021 07 23; 433(15):167090.J Mol Biol2021-06-04T00:00:002021Inhibition of Cancer Cell Adhesion, Migration and Proliferation by a Bispecific Antibody that Targets two Distinct Epitopes on av Integrins.34438094Simons E, Labro A, Saenen J, Nijak A, Sieliwonczyk E, Vandendriessche B, Dabrowska M, Van Craenenbroeck EM, Schepers D, Van Laer L, Loeys BL, Alaerts MEuropean journal of medical geneticsMolecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death. Eur J Med Genet. 2021 Nov; 64(11):104322.Eur J Med Genet2021-08-23T00:00:002021Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death.35583973Wei AD, Wakenight P, Zwingman TA, Bard AM, Sahai N, Willemsen MH, Schelhaas HJ, Stegmann APA, Verhoeven JS, de Man SA, Wessels MW, Kleefstra T, Shinde DN, Helbig KL, Basinger A, Wagner VF, Rodriguez-Buritica D, Bryant E, Millichap JJ, Millen KJ, Dobyns WB, Ramirez JM, Kalume FKJournal of neurophysiologyHuman KCNQ5 de novo mutations underlie epilepsy and intellectual disability. J Neurophysiol. 2022 07 01; 128(1):40-61.J Neurophysiol2022-05-18T00:00:002022Human KCNQ5 de novo mutations underlie epilepsy and intellectual disability.36721196Sieliwonczyk E, Alaerts M, Simons E, Snyders D, Nijak A, Vandendriessche B, Schepers D, Akdeniz D, Van Craenenbroeck E, Knaepen K, Rabaut L, Heidbuchel H, Van Laer L, Saenen J, Labro AJ, Loeys BOrphanet journal of rare diseasesClinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population. Orphanet J Rare Dis. 2023 01 31; 18(1):23.Orphanet J Rare Dis2023-01-31T00:00:002023Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.http://voices.uchicago.edu/wtang-lab/Wei-Jen Tang laboratory siteUniversity of ChicagoAlainLabroAlain J. Labro41.78927490000000-87.601250000000001296Labro, AlainAkitoNatsumeAkito Natsume41.78927490000000-87.601250000000002454Natsume, AkitoDavidGrdinaDavid Grdina41.78927490000000-87.60125000000000255Grdina, DavidProfessorWei-JenTangWei-Jen Tang41.78927490000000-87.60125000000000957Tang, Wei-JenProfessortrue1true1true1ProfessorProfessortrue1PROFESSOR PROFESSOR true1ProfessorProfessor