D003181Chemicals & DrugsD12.776.124.486.274.3509100.994387Complement C4prns:emailEncryptedemail addressFaculty Rankprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasFacultyRankhas faculty rankprns: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 ResourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonMichaelCharltonMichael Charlton0.000000000000000.000000000000003423Charlton, MichaelProfessor0.5151050.00877779research area of0.5180130.0088272612subject area forMedicine-GastroenterologyPediatrics-Allergy & Immunology22886582Chen W, Xu Z, Nishitani M, Van Ryzin C, McDonnell NB, Merke DPHuman geneticsComplement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Genet. 2012 Dec; 131(12):1889-94.Hum Genet2012-08-12T00:00:002012Complement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.9461092Quigg RJ, Lim A, Haas M, Alexander JJ, He C, Carroll MCKidney internationalImmune complex glomerulonephritis in C4- and C3-deficient mice. Kidney Int. 1998 Feb; 53(2):320-30.Kidney Int1998-02-01T00:00:001998Immune complex glomerulonephritis in C4- and C3-deficient mice.Radiology-Thoracic ImagingMedicinePathologyUniversity of ChicagoPeterPytelx3JwH6QZOfnamXNnYUHhvWD+6g==Peter Pytel41.78927490000000-87.601250000000001091Pytel, PeterProfessorRichardQuiggRichard Quigg41.78927490000000-87.60125000000000527Quigg, RichardEmeritus/Emerita, ProfessorFurkanUfukFurkan Ufuk41.7886000000000087.598699999999994519Ufuk, FurkanAssistant Professor26458084Ufuk F, Herek D, Karabulut NJournal of gastroenterology and hepatologyEducation and Imaging: Gastroenterology: A rare cause of acute abdomen, hereditery angioedema. J Gastroenterol Hepatol. 2015 Nov; 30(11):1561.J Gastroenterol Hepatol2015-11-01T00:00:002015Education and Imaging: Gastroenterology: A rare cause of acute abdomen, hereditery angioedema.true1Emeritus/Emerita, ProfessorEmeritus/Emerita, Professortrue1ProfessorProfessortrue1ProfessorProfessortrue1Associate ProfessorAssociate Professortrue1Assistant ProfessorAssistant Professor24897075Pytel PApplied immunohistochemistry & molecular morphology : AIMMC4d staining as immunohistochemical marker in inflammatory myopathies. Appl Immunohistochem Mol Morphol. 2014 Oct; 22(9):696-704.Appl Immunohistochem Mol Morphol2014-10-01T00:00:002014C4d staining as immunohistochemical marker in inflammatory myopathies.1010ChristinaCiaccioChristina Ciaccio0.000000000000000.000000000000003181Ciaccio, ChristinaAssociate Professor22073494Ciaccio CEMissouri medicineAngioedema: an overview and update. Mo Med. 2011 Sep-Oct; 108(5):354-7.Mo Med2011-09-01T00:00:002011Angioedema: an overview and update.