Generation of a Col9A3 exon 3 skipping mouse as a novel model to phenocopy multiple epiphyseal dysplasia patients

Lecci S.; Briggs M. D.; Rowan A. D.; Young D. A.

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Generation of a Col9A3 exon 3 skipping mouse as a novel model to phenocopy multiple epiphyseal dysplasia patients

机译：生成COL9A3外显子3跳过鼠标作为一种新型模型，以缺陷多种骨骺发育不良患者

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来源
《International Journal of Experimental Pathology》 |2017年第3期|共1页
作者
Lecci S.; Briggs M. D.; Rowan A. D.; Young D. A.;
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Newcastle Univ Int Ctr Life Inst Genet Med Skeletal Res Grp Newcastle Upon Tyne NE1 3BZ Tyne &

Newcastle Univ Int Ctr Life Inst Genet Med Skeletal Res Grp Newcastle Upon Tyne NE1 3BZ Tyne &

Newcastle Univ Int Ctr Life Inst Genet Med Skeletal Res Grp Newcastle Upon Tyne NE1 3BZ Tyne &

Newcastle Univ Int Ctr Life Inst Genet Med Skeletal Res Grp Newcastle Upon Tyne NE1 3BZ Tyne &

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正文语种 eng
中图分类病理学;
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1. Five patients in a Chinese family with multiple epiphyseal dysplasia [J] . LIU Feng-xia, YU Meng-xue, LI Yong-zhe, 中华医学杂志（英文版） . 2009,第017期
2. Diagnosis with Multiple Epiphyseal Dysplasia Using Whole-exome Sequencing in a Chinese Family [J] . Hong-Yan Liu, Ji-Fang Xiao, Jia Huang, 中华医学杂志（英文版） . 2017,第001期
3. EDM1: a novel point mutation in cartilage oligomeric matrix protein gene in a Chinese family with multiple epiphyseal dysplasia [J] . LIU Feng-xia, LI Yan-xiang, ZHANG Xu-de, 中华医学杂志（英文版） . 2013,第006期
4. Generation of a Col9A3 exon 3 skipping mouse as a novel model to phenocopy multiple epiphyseal dysplasia patients [J] . Lecci S., Briggs M. D., Rowan A. D., International Journal of Experimental Pathology . 2017,第3期

机译：生成COL9A3外显子3跳过鼠标作为一种新型模型，以缺陷多种骨骺发育不良患者
5. A Col9a3 exon 3 skipping mouse as a novel model for multiple epiphyseal dysplasia [J] . Lecci S., Miles C., Cairns P., International Journal of Experimental Pathology . 2019,第4期

机译：COL9A3外显子3跳过鼠标作为多种骨骺发育不良的新模型
6. A COL9A3 EXON 3 SKIPPING MOUSE AS NOVEL MODEL FOR MULTIPLE EPIPHYSEAL DYSPLASIA AND EARLY-ONSET OSTEOARTHRITIS [J] . Lecci S., Miles C. G., Briggs M. D., Osteoarthritis and cartilage . 2018,第Suppla1期

机译：COL9A3 EXON 3跳过鼠标作为多种骨骺发育不良和早期骨关节炎的新型模型
7. Development of pharmacodynamic biomarkers for Duchenne muscular dystrophy using exon skipping treatment and mdx mouse model. [C] . Haeri Seol, Meng H Han, Aiping Zhang, ASMS Conference on Mass Spectrometry and Allied Topics . 2015

机译：外显子跳跃治疗和MDX小鼠模型的Duchenne肌营养不良药物动力学生物标志物的发展。
8. Characterizing the effect of mutations within exon 7 of the murine survival motor neuron gene to model spinal muscular atrophy in the mouse. [D] . Hammond, Suzan Michelle. 2010

机译：表征小鼠存活运动神经元基因外显子7内突变对小鼠脊髓性肌萎缩模型的影响。
9. An unfolded protein response is the initial cellular response to the expression of mutant matrilin-3 in a mouse model of multiple epiphyseal dysplasia [O] . Seema Nundlall, M. Helen Rajpar, Peter A. Bell, 2010

机译：展开的蛋白质反应是在多发性骨发育不良的小鼠模型中对突变体matrilin-3表达的初始细胞反应
10. Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation [O] . Bell, Peter A., Pirõg, Katarzyna A., Fresquet, Maryline, 2012

机译：matrilin 1的丢失不会加剧由matn3 V194D突变引起的多发性骨骺发育不良的小鼠模型中的骨骼表型
11. Developing a Mouse Model of Sensory and Cognitive Deficits for Multiple Sclerosis. [R] . Gow, A., Diamond, B. 2012

机译：开发多发性硬化症的感觉和认知缺陷的小鼠模型。

Generation of a Col9A3 exon 3 skipping mouse as a novel model to phenocopy multiple epiphyseal dysplasia patients

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