Quantitative analysis on developmental morphologic changes on mandibles of Apert syndrome mice
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Quantitative analysis on developmental morphologic changes on mandibles of Apert syndrome mice
Journal of Army Medical UniversityVol. 31, Issue 17, Pages: 1625-1628(2009)
作者机构:
1. 第三军医大学大坪医院野战外科研究所全军战创伤中心,创伤、烧伤与复合伤国家重点实验室
2. 四川省绵阳市疾病预防控制中心微生物所
作者简介:
基金信息:
DOI:
CLC:R782.23;R195.2;R323.1
Published:2009,
Published Online:15 September 2009,
稿件说明:
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DU XIAO-LAN, CHEN ZHI, YIN LIANG-JUN, et al. Quantitative analysis on developmental morphologic changes on mandibles of Apert syndrome mice. [J]. Journal of army medical university, 2009, 31(17): 1625-1628.
DOI:
DU XIAO-LAN, CHEN ZHI, YIN LIANG-JUN, et al. Quantitative analysis on developmental morphologic changes on mandibles of Apert syndrome mice. [J]. Journal of army medical university, 2009, 31(17): 1625-1628.DOI:
Quantitative analysis on developmental morphologic changes on mandibles of Apert syndrome mice
Objective To compare and analyze the morphologic and growth difference between the mandibles of the mouse carrying Ser252Trp mutation in fibroblast growth factor receptor (FGFR2) which was regarded as a model for human Apert syndrome
and of their wild type controls. Methods The 3-D coordinate data of 11 landmarks of the mandible were collected by a 3-D coordinate measuring machine. Data were analyzed using Euclidean distance matrix analysis (EDMA) to quantitatively compare the morphologic and growth difference between the mandibles of mutants and their controls. Results At 4 weeks old
the mutants’ mandible was smaller than their wild
type control
and there was no statistical difference between them (
P
>0.05). The mandible was much smaller in the mutants than their wild type controls
with a statistical difference when they were 8 weeks old (
P
<
0.05). The major abnormality in the mutants was the anteriorly displaced coronoid process and mandibular angle along anterio-posterior axis
which becomes more severe with age. Conclusion The reducing of the mutants’ mandibles becomes more severe with age.
Skull morphology of mice carrying gain-of-function mutation of FGFR2 Ser252Trp by Euclidean distance matrix analysis
Establishment of mouse model of immune tolerance of asthma through subcutaneous injection of high dose of ovalbumin
Construction of intrahepatic transplantation model of hepatic progenitors cells expressing hepatitis B virus X in mice
Construction and otological phenotypic characterization of a mouse model harboring orthologous human Waardenburg syndrome mutation SOX10 p.R106W
Related Author
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FENG Tao
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Related Institution
State Key Laboratory of Trauma, Burns and Combined Injury, Trauma Center, Institute of Surgery Research, Daping Hospital, Third Military Medical University
Molecular Medicine and Cancer Research Centre, Center for Biochemistry and Molecular Biology, College of Basic Medical Sciences, Chongqing Medical University
Department of Pediatrics, Laboratory of Cardiothoracic Surgery, Southwest Hospital, Third Military Medical University
Research Center of Molecular Medicine and Cancer, Center of Biochemistry and Molecular Biology, Department of Pathophysiology, College of Basic Medical Sciences, Chongqing Medical University
Department of Laboratory Animal Science, College of Basic Medical Sciences, Army Medical University (Third Military Medical University)