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Integrative analysis of SEPN1 in glioma: Prognostic roles, functional implications, and potential therapeutic interventions.
Wang Z, Wang D, Wang X, Xu Y, Yuan Y, Chen Y, Li Z, Liu X. Wang Z, et al. PLoS One. 2025 Feb 7;20(2):e0318501. doi: 10.1371/journal.pone.0318501. eCollection 2025. PLoS One. 2025. PMID: 39919065 Free PMC article.
We developed an SEPN1-related risk score (SRS) based on SEPN1-related long non-coding RNAs and validated its prognostic value. ...Enrichment analysis indicated the involvement of SEPN1 in immune-related processes and signaling pathways. Suppressing SEPN1 …
We developed an SEPN1-related risk score (SRS) based on SEPN1-related long non-coding RNAs and validated its prognostic value. …
Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from India.
Chawla T, Nashi S, Baskar D, Polavarapu K, Vengalil S, Bardhan M, Preethish-Kumar V, Sukrutha R, Unnikrishnan G, Huddar A, Padmanabha H, Anjanappa RM, Bevinahalli N, Nittur V, Rajanna M, Arunachal Udupi G, Nalini A. Chawla T, et al. Neurogenetics. 2024 Oct;25(4):435-469. doi: 10.1007/s10048-024-00776-6. Epub 2024 Aug 5. Neurogenetics. 2024. PMID: 39103709
Other CMDs identified were LAMA2-RD (26%), alpha-dystroglycan-RD (19%), LMNA-RD (8%), CHKB-RD (7%) and SEPN1-RD (3%). Similar to previous cohorts, overall, missense variants were common in COL-6 RD. ...
Other CMDs identified were LAMA2-RD (26%), alpha-dystroglycan-RD (19%), LMNA-RD (8%), CHKB-RD (7%) and SEPN1-RD (3%). Similar to prev …