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searching for WNT10A 5 found (15 total)

alternate case: wNT10A

KRT84 (67 words) [view diff] exact match in snippet view article find links to article

Horrell J, Snitow M, Cui J, Gochnauer H, Syrett CM, et al. (June 2017). "WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation

Taurodontism (1,011 words) [view diff] case mismatch in snippet view article find links to article

(2015). "Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds". Molecular Genetics & Genomic Medicine. 3

DNAJB2 (680 words) [view diff] exact match in snippet view article find links to article

PMC 1430359. PMID 16604191. Adaimy L, Chouery E, Megarbane H (2007). "Mutation in WNT10A Is Associated with an Autosomal Recessive Ectodermal Dysplasia: The Odonto-onycho-dermal

Anodontia (1,970 words) [view diff] exact match in snippet view article find links to article

MSX1, PAX9, IRF6, GREM2, AXIN2, LRP6, SMOC2, LTBP3, PITX2, and WNT10B. The WNT10A gene is considered to be the major gene involved in hypodontia and oligodontia

Hypodontia (7,611 words) [view diff] exact match in snippet view article find links to article

MSX1 4p16 STHAG2 602639 ? 16q12 STHAG3 604625 PAX9 14q12 STHAG4 150400 WNT10A 2q35 STHAG5 610926 ? 10q11 STHAG6 613097 LTBP3 11q12 STHAGX1 313500 EDA