Varaico: Literature-Extracted Genetic Variants

Gene:MSX2
Variant:p.F149F
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MSX2

NM_002449.5:p.F149F

Associated Papers

Overexpression of miR-1306-5p, miR-3195, and miR-3914 Inhibits Ameloblast Differentiation through Suppression of Genes Associated with Human Amelogenesis Imperfecta.

Yoshioka H et al.

International Journal of Molecular Sciences, 2021

33672174 (PubMed )
Supplement: ijms-22-02202-s001.zip › Supplementary_Table_S4-1_Final_021921.xlsx › Table_S3.1

Molecular genetics of ameloblast cell lineage.

Bei M

Journal of Experimental Zoology. Part B, Molecular and Developmental Evolution, 2009

A case of amelogenesis imperfecta, cleft lip and palate and polycystic kidney disease.

Suda N et al.

Orthodontics & Craniofacial Research, 2006

The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvement.

Bailleul-Forestier I et al.

European Journal of Medical Genetics, 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."