26437028Guimier A, Gabriel GC, Bajolle F, Tsang M, Liu H, Noll A, Schwartz M, El Malti R, Smith LD, Klena NT, Jimenez G, Miller NA, Oufadem M, Moreau de Bellaing A, Yagi H, Saunders CJ, Baker CN, Di Filippo S, Peterson KA, Thiffault I, Bole-Feysot C, Cooley LD, Farrow EG, Masson C, Schoen P, Deleuze JF, Nitschk? P, Lyonnet S, de Pontual L, Murray SA, Bonnet D, Kingsmore SF, Amiel J, Bouvagnet P, Lo CW, Gordon CTNature geneticsBody Patterning; Heterotaxy Syndrome; Matrix Metalloproteinases, Secreted; Point Mutation; VertebratesAnimals; Embryo, Nonmammalian; Family Health; Female; Gene Expression Regulation, Developmental; Genes, Recessive; Heart; Heart Defects, Congenital; Humans; In Situ Hybridization; Male; Mice; Pedigree; Sequence Analysis, DNA; Zebrafish; Zebrafish ProteinsGuimier A, Gabriel GC, Bajolle F, Tsang M, Liu H, Noll A, Schwartz M, El Malti R, Smith LD, Klena NT, Jimenez G, Miller NA, Oufadem M, Moreau de Bellaing A, Yagi H, Saunders CJ, Baker CN, Di Filippo S, Peterson KA, Thiffault I, Bole-Feysot C, Cooley LD, Farrow EG, Masson C, Schoen P, Deleuze JF, Nitschk? P, Lyonnet S, de Pontual L, Murray SA, Bonnet D, Kingsmore SF, Amiel J, Bouvagnet P, Lo CW, Gordon CT. MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates. Nat Genet. 2015 Nov; 47(11):1260-3.Nat Genet2015-10-05T00:00:002015MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates.cmhprofilesont:personsuffixperson suffixprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:hasSubjectAreaMajorTopicListhas major subject area listprns:hasSubjectAreaMinorTopicListhas minor subject area listprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:positionInDepartmentposition in departmentprns:positionInDivisionposition in divisionprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed Identifiervivo:authorRankauthor rank in publicationAuthorshipDepartmentDivisionvivo:hasSubjectAreahas subject areavivo:hrJobTitleHR job titleInformation Resourcevivo:informationResourceInAuthorshipauthorsvivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonD008297Physiology11633280.54802MaleD010375Concepts & Ideas22560.983861PedigreeD014714Living Beings110.999306VertebratesD015027Living Beings460.998753ZebrafishD017354Physiology440.998573Point MutationD017403Procedures580.999048In Situ HybridizationD017422Procedures301150.947191Sequence Analysis, DNAD018507Physiology13550.966672Gene Expression Regulation, DevelopmentalD019521Physiology110.999306Body PatterningD029961Chemicals & Drugs110.999826Zebrafish ProteinsPhD, CGCEmilyFarrowEmily G. Farrow0.000000000000000.00000000000000124Farrow, EmilyDirector of Lab OperationsAuthorship 3742230.2779520.1389762authors10.2521has subject areaD051379Living Beings513120.910614MiceD053505Chemicals & Drugs110.999306Matrix Metalloproteinases, SecretedD059446Disorders110.999306Heterotaxy SyndromePediatricsClinicalChildren's Mercy Kansas CityAuthorship 6551D000818Living Beings726640.834746Animalstrue1Director of Lab OperationsDirector of Lab OperationsD004625Anatomy110.999826Embryo, NonmammalianD005192Concepts & Ideas9140.992713Family HealthD005260Physiology11835990.534568FemaleD005808Genes & Molecular SequencesPhenomena260.99461Genes, RecessiveD006321Anatomy11170.981788HeartD006330Disorders25820.906648Heart Defects, CongenitalD006801Living Beings12067970.397999Humans