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Plasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patients

dc.creatorParsopoulou F., Charignon D., Tengo M., Psarros F., Maas C., Gonzalez-Quevedo T., Drouet C., Germenis A.E., Ghannam A.en
dc.date.accessioned2023-01-31T09:46:00Z
dc.date.available2023-01-31T09:46:00Z
dc.date.issued2020
dc.identifier10.1111/all.14280
dc.identifier.issn01054538
dc.identifier.urihttp://hdl.handle.net/11615/77956
dc.description.abstract[No abstract available]en
dc.language.isoenen
dc.sourceAllergy: European Journal of Allergy and Clinical Immunologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85082958102&doi=10.1111%2fall.14280&partnerID=40&md5=91905cdef7050e0c9d71974eff8ebe09
dc.subjectaminopeptidase Pen
dc.subjectbiological markeren
dc.subjectcitric aciden
dc.subjectenzyme precursoren
dc.subjectglutamic aciden
dc.subjecthigh molecular weight kininogenen
dc.subjectlysineen
dc.subjectplasminen
dc.subjectplasminogenen
dc.subjectreceptoren
dc.subjects100a10 receptoren
dc.subjectstreptokinaseen
dc.subjecttissue plasminogen activatoren
dc.subjecttranexamic aciden
dc.subjectunclassified drugen
dc.subjecturokinaseen
dc.subjectplasminogenen
dc.subjectangioneurotic edemaen
dc.subjectcell componenten
dc.subjectconformational transitionen
dc.subjectgene frequencyen
dc.subjectgenetic polymorphismen
dc.subjectgenetic variabilityen
dc.subjectheterozygoteen
dc.subjecthomozygosityen
dc.subjecthumanen
dc.subjectimmunoblottingen
dc.subjectLetteren
dc.subjectmissense mutationen
dc.subjectmolecular weighten
dc.subjectpedigreeen
dc.subjectpenetranceen
dc.subjectplasminogen activationen
dc.subjectpriority journalen
dc.subjectprotein glycosylationen
dc.subjectangioneurotic edemaen
dc.subjectgeneticsen
dc.subjectmissense mutationen
dc.subjectAngioedemas, Hereditaryen
dc.subjectHumansen
dc.subjectMutation, Missenseen
dc.subjectPlasminogenen
dc.subjectBlackwell Publishing Ltden
dc.titlePlasminogen glycoforms alteration and activation susceptibility associated with the missense variant p.Lys330Glu in HAE-PLG patientsen
dc.typeotheren


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