논문KCI 등재
어퍼트 및 크루즌 증후군을 유발하는 골조직 특이성 FGFR2 돌연변이에 의한 두개안면 형태의 변화
Craniofacial morphologic alteration induced by bone-targeted mutants of FGFR2 causing Apert and Crouzon syndrome
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-어퍼트 및 크루즌 증후군을 유발하는 골조직 특이성 FGFR2 돌연변이에 의한 두개안면 형태의 변화
참고문헌 (41)
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- "Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2", 8, pp.275~279 (1994)
- "Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome", 8, pp.98~103 (1994)
- "Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome", 9, pp.165~172 (1995)
- "Activating (P253R, C278F) and dominant negative mutations of FGFR2: differential effects on calvarial bone cell proliferation, differentiation, and mineralization", 44, pp.292~297 (2003)
- "Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault", 126, pp.5611~5620 (1999)
- "The IIIc alternative of FGFR2 is a positive regulator of bone formation", 129, pp.3783~3793 (2002)
- "Craniosynostosis: genes and mechanisms", 6, pp.1647~1656 (1997)
- "Transforming growth factor beta s and fibroblast growth factors and their receptors: role in sutural biology and craniosynostosis", 12, pp.322~331 (1997)
- "Comparative study of normal, Crouzon, and Apert craniofacial morphology using finite element scaling analysis", 74, pp.473~493 (1987)
- "Generation of transgenic mouse model to study cranial suture developement: Apert syndrome", 33, pp.485~497 (2003)
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- "Effect of fibroblast growth factor on cultured fetal rat calvaria", 29, pp.108~114 (1980)
- "The interaction of heparin and basic fibroblast growth factor on collagen synthesis in 21-day fetal rat calvariae", 130, pp.2675~2682 (1992)
- "A Ser250Trp substitution in mouse fibroblast growth factor receptor 2(Fgfr2) results in craniosynostosis", 33, pp.169~178 (2003)
- "Is the mandible intrinsically different in Apert and Crouzon syndromes?", 85, pp.475~487 (1984)
- "Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation", 24, pp.391~395 (2000)
- "Fibroblast growth factors lead to increased Msx2 expression and fusion in calvarial sutures", 18, pp.751~759 (2003)
- "Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice", 217, pp.137~145 (2000)
- "Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes", 21, pp.181~188 (1993)
- "Cephalometric study of the Apert syndrome in adolesconce and adulthood", 19, pp.1~11 (1999)
- "Crouzon syndrome: cephalometric analysis and evaluation of pathogenesis", 31, pp.201~209 (1994)
- "The pathogenesis of premature craniosynostosis in acrocephalosyndactyly (Apert's syndrome). A reconsideration", 59, pp.699~707 (1977)
- "Cranial base deformity in Apert's syndrome", 69, pp.254~263 (1982)
- "The role of the cranial base in facial growth: experimental craniofacial synsostosis in the rabbit", 99, pp.1396~1407 (1997)
- "The cranial base angle and maxillary hypoplasia in unoperated Crouzon patients", 7, pp.69~70 (1996)
- "Apert's syndrome: cephalometric evaluation and considerations on pathogenesis", 7, pp.23~31 (1996)
- "Age changes in the human frontozygomatic suture from 20 to 95 years", 69, pp.411~430 (1976)
- "Genotype-phenotype analysis in Apert syndrome suggests opposite effects of the two recurrent mutations on syndactyly and outcome of craniofacial surgery", 57, pp.137~139 (2000)
- "Receptor specificity of the fibroblast growth factor family", 271, pp.15292~15297 (1996)
- "Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome", 97, pp.14536~14541 (2000)
- "Maxillary growth following LeFort III advancement surgery in Crouzon, Apert, and Pfeiffer syndromes", 90, pp.420~430 (1986)
관련 논문AI추천
두개봉합 발육 연구를 위한 형질변환 쥐의 개발 : 어퍼트 신드롬나현덕, 박광균, 박영철, 백형선, 이기준, RatisoontornC대한치과교정학회 · 대한치과교정학회지2003 · 제33권 제6호Crouzon 증후군 환자의 증례보고김영재, 김정욱, 김종철, 이상훈, 이수진, 장기택, 한세현대한소아치과학회 · 대한소아치과학회지2009 · 제36권 제1호Apert 증후군과 Pfeiffer 증후군: 2례 보고윤선영, 윤신원, 정희정대한소아신경학회 · 대한소아신경학회지2013 · 제21권 제3호Apert syndrome : 증례보고박광선, 박호원, 서현우, 이주현대한소아치과학회 · 대한소아치과학회지2008 · 제35권 제3호한국인 비증후군성 구순구계열 환자의 OFC1 유전자의 서열 분석김성식, 손우성대한치과교정학회 · 대한치과교정학회지2003 · 제33권 제3호구순구개열 태아의 비정상적인 상악골 성장형태에 대한 연구김성민, 김정환, 김지혁, 박영욱, 이석근, 이종호대한구강악안면외과학회 · 대한구강악안면외과학회지2007 · 제33권 제3호
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