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MSX2 protein

mutation in the homeodomain of the human MSX2 gene occurs in a family affected with autosomal dominant craniosynostosis, Boston type; aa sequence given in first source
Also Known As:
MSX-2 protein; MSX2 protein, human; Msx2 protein, mouse; Msx2 protein, rat; homeo box, msh-like 2 protein, mouse; msh homeo box homolog 2 (Drosophila) protein, rat; msh homeo box homolog 2 (Drosophila), human
Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Aleksic, Branko: 1 article (01/2020)
2. Hirose, Shinichi: 1 article (01/2020)
3. Inoue, Yushi: 1 article (01/2020)
4. Iwayama, Yoshimi: 1 article (01/2020)
5. Kaneko, Sunao: 1 article (01/2020)
6. Kano, Masanobu: 1 article (01/2020)
7. Kushima, Itaru: 1 article (01/2020)
8. Matsumoto, Naomichi: 1 article (01/2020)
9. Mazaki, Emi: 1 article (01/2020)
10. Miyake, Noriko: 1 article (01/2020)

Related Diseases

1. Prostatic Neoplasms (Prostate Cancer)
2. Partial Epilepsies (Epilepsy, Partial)
3. Craniosynostoses (Craniosynostosis)

Related Drugs and Biologics

1. Ubiquitin-Protein Ligases (Ubiquitin-Protein Ligase)