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Keyword [Cleidocranial Dysplasia]
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1. Mutation Analysis Of RUNX2 Gene In Chinese Patients With Cleidocranial Dysplasia And Related Function Analysis
2. Genetic Analysis For Two Cleidocranial Dysplasia Families
3. The Research On Biological Behaviors Of BMMSCs And DPSCs Derived From A Patient With Cleidocranial Dysplasia
4. Role Of Core Binding Factor Beta In Bone And Cartilage Development
5. Possible Mechanism Of Crosstalk Between MicroRNA And RUNX2gene In Human Dental Follicle Cells
6. Clinical And Basic Studies On Cleidocranial Dysplasia
7. Orthodontic Treatment In A Patient With Congenita Cleidocranial Dysplasia Syndrome
8. Cleidocranial Dysplasia:a Review Of Literature And Five Case Reports
9. Study Of Tooth Eruption Via RUNX2-MiR-31-SATB2 Loop In Dental Follicle Cells
10. Research On The Clinical Characteristics And Disease-causing Mechanisms In A Chinese Family With Cleidocranial Dysplasia
11. Study Of The Role Of MicroRNA-31 In The Biological Characteristics Of Bone Marrow Stromal Cells From Cleidocranial Dysplasia
12. Orthodontic Treatment Of Impacted Teeth In Patients With Cleidocranial Dysplasia Syndrome
13. MTOR/Raptor-S6k1 Signaling Pathway Promote Skeletogenesis And Bone Development Via Runx2 In Mice
14. A Research On The Pathogenic Mechanism Of A Family With Cleidocranial Dysplasia
15. Generation And Identification Of Induced Pluripotent Stem Cells From Cord Blood Of Two Kinds Of Skeletal Dysplasia Fetuses
16. Orthodontic Treatment And Genetic Analysis In Patients With Cleidocranial Dysplasia Of A Family
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