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Functional Charaterization of a Novel FGFR2 Mutation, E731K, in Craniosynostosis : 두개골 조기 유합증에서 FGFR2의 Novel Mutation인 E731K의 역할 규명

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dc.contributor.advisor류현모-
dc.contributor.author박정현-
dc.date.accessioned2009-12-31T07:46:47Z-
dc.date.available2009-12-31T07:46:47Z-
dc.date.copyright2009.-
dc.date.issued2009-
dc.identifier.urihttp://dcollection.snu.ac.kr:80/jsp/common/DcLoOrgPer.jsp?sItemId=000000037626eng
dc.identifier.urihttps://hdl.handle.net/10371/24627-
dc.descriptionThesis(masters) --서울대학교 대학원 :치의학과 (구개악안면세포 및 발생생물학전공),2009.2.en
dc.format.extent31 leavesen
dc.language.isoenen
dc.publisher서울대학교 대학원en
dc.subject두개골 조기 유합증en
dc.subjectCraniosynostosisen
dc.subjectApert syndromeen
dc.subjectApert syndromeen
dc.subjectFGFR2en
dc.subjectFGFR2en
dc.subjectPhosphorylationen
dc.subjectphosphorylationen
dc.subjectRunx2en
dc.subjectERK pathwayen
dc.subjectRunx2en
dc.titleFunctional Charaterization of a Novel FGFR2 Mutation, E731K, in Craniosynostosisen
dc.title.alternative두개골 조기 유합증에서 FGFR2의 Novel Mutation인 E731K의 역할 규명en
dc.typeThesis-
dc.contributor.department치의학과 (구개악안면세포 및 발생생물학전공)-
dc.description.degreeMasteren
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