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. 2024 Oct 28;25(21):11572. doi: 10.3390/ijms252111572

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© 2024 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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HAO1 mRNA expression and its association with clinicopathological parameters and molecular subtypes in the METABRIC cohort was analysed using the one-way analysis of variance (ANOVA) with the post hoc Tukey test and using bc-GenExMiner, according to (A,B) ER, (C,D) PR, (E,F) ER/PR, (G,H) PAM50 subtype, (I) Size, (J) Grade, (K) Lymph Node Stage, and (L) Integrative Cluster. METABRIC cohort was analysed using the one-way analysis of variance (ANOVA) with the post hoc Tukey test. Statistically significant p-values shown in bold. *** p < 0.0001; ** p < 0.001; * p < 0.01.

HAO1 mRNA expression and its association with clinicopathological parameters and molecular subtypes in the METABRIC cohort was analysed using the one-way analysis of variance (ANOVA) with the post hoc Tukey test and using bc-GenExMiner, according to (A,B) ER, (C,D) PR, (E,F) ER/PR, (G,H) PAM50 subtype, (I) Size, (J) Grade, (K) Lymph Node Stage, and (L) Integrative Cluster. METABRIC cohort was analysed using the one-way analysis of variance (ANOVA) with the post hoc Tukey test. Statistically significant p-values shown in bold. *** p < 0.0001; ** p < 0.001; * p < 0.01.