Papillorenal syndrome (PAPRS), or renal coloboma syndrome, is a rare autosomal dominant disorder caused by PAX2 mutation...
...PAX2, COQ8B or INF2, causing hereditary steroid-resistant nephrotic syndrome, led to significantly earlier ESKD onset (m...
...Pax2 knockdown mice via injection of AAV-shPax2 virus and comprehensively evaluated ASD-related behaviors, revealing aut...
...PAX2. Alcian blue-periodic acid-Schiff staining was positive. No KRAS mutations were detected.ConclusionCervical MGH is ...
...Pax2-positive mesenchymal population, suggesting an ancestral condition in Archelosauria that differs from the primarily...
...PAX2 loss (3/4), nuclear β-catenin (1/3), and decreased PTEN (2/3); molecular analysis on 2 cases revealed TP53 loss of ...
...PAX2, TSC2, and UMOD, while 39% remained genetically unresolved. Patients with non-ADPKD diagnoses typically showed mult...
...PAX2), otofaciocervical syndrome with immunodeficiency (PAX1), Waardenburg syndrome (PAX3), maturity-onset diabetes of t...
...PAX2-PAX7) levels. These findings establish PAX transcription factors as key modulators of breast cancer biology and sup...
...PAX2 and BCL6 transcription factors were significantly enriched. The identified clusters were validated across six indep...
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