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Publications by Kwang-Hwi Cho
The Boston-Type Craniosynostosis Mutation MSX2 (P148H) Results in Enhanced Susceptibility of MSX2 to Ubiquitin-Dependent Degradation
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Parietal Foramina With Cleidocranial Dysplasia Is Caused by Mutation in MSX2
European Journal of Human Genetics
Genetics
Msx2 and Foxn1 Regulate Nail Homeostasis
Genesis
Medicine
Endocrinology
Genetics
Cell Biology
Moleculer Analysis of Fgfr1-3, Twist1, Msx2, Por, Frem1 and Rab23 Genes in Syndromic and Non-Syndromic Craniosynostosis Cases
İstanbul Tıp Fakültesi Dergisi
Accelerated Closure of Skin Wounds in Mice Deficient in the Homeobox Gene Msx2
Wound Repair and Regeneration
Dermatology
Surgery
Functional and Prognostic Relevance of the Homeobox Protein MSX2 in Malignant Melanoma
British Journal of Cancer
Cancer Research
Oncology
Reciprocal Roles of Msx2 in Regulation of Osteoblast and Adipocyte Differentiation
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Msx2 Promotes Cardiovascular Calcification by Activating Paracrine WNT Signals
Journal of Clinical Investigation
Medicine
Msx2 Supports Epidermal Competency During Wound Induced Hair Follicle Neogenesis
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
MINT, the Msx2 Interacting Nuclear Matrix Target, Enhances Runx2-Dependent Activation of the Osteocalcin Fibroblast Growth Factor Response Element
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology