...PAX2, and CTNNB1 as hub genes (Pearson r = 0.868 between module scores, P < 0.001). The developmental module showed the ...
...Pax2 may have subsumed the role of Pax6 in eye fate specification in chelicerates. However, no functional data are avail...
...PAX2, WT1 variants, and 17q12 deletion as the most prevalent pathogenic variations. This study reveals distinct clinical...
...PAX2, TSC2, and UMOD, while 39% remained genetically unresolved. Patients with non-ADPKD diagnoses typically showed mult...
...pax2a-/- mutants. Misexpression of cdh1/Ecad in pax2a-/- mutants partially rescues pax2a-/- mutants. Elevating β-catenin...
...PAX2. One of 5 cases (20%) of endometriosis with atypia was marker-aberrant (both PAX2 and PTEN), supporting prior findi...
...PAX2 genes, which play critical roles in eye development. MGS is often linked with other ocular and systemic anomalies, ...
...PAX2 ( P G×Age =4.22×10 -8 ), MAP and language with LOC105371656 ( P G×Age =1.75×10 -8 ), and DBP and language with SUFU...
...pax2, pax6a, and pax6b), apoptosis (tp53, casp3, bax, and bcl2a), and antioxidant defense (sod1, cat, and gpx1a). VitE c...
...PAX2 pathogenic variants c.685C>T and c.250G>A, highlighting the diverse phenotypic expression of PAX2-related disorders...
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