SR-BI deficiency inhibits melanogenesis by attenuating the PKA/CREB signaling axis: Implications for vitiligo

Genes and Diseases · Published 2026-07-01 · DOI 10.1016/j.gendis.2026.102350

Free full text

Authors (5)

Linli Liu, Daopei Zou, Yihuan Pu, Xinyi Shao, Jin Chen

Abstract

PubPorta does not have an abstract for this article yet.

Read the article at the publisher →

Publication details

Year

2026

Citation

Liu, L., Zou, D., Pu, Y., et al. (2026). SR-BI deficiency inhibits melanogenesis by attenuating the PKA/CREB signaling axis: Implications for vitiligo. Genes and Diseases. https://doi.org/10.1016/j.gendis.2026.102350

Related articles

• Charting the landscape of microbiota in bladder cancer: Molecular mechanisms and therapeutic implications · Genes and Diseases · 2026 · Same journal
• Mitochondrial DNA mutation associations with ERK/MAPK inhibitor sensitivity in cancer · Genes and Diseases · 2026 · Same journal
• Role of post-translational modifications in cancer metabolic reprogramming · Genes and Diseases · 2026 · Same journal
• SASH3 mutations cause monogenic inflammatory bowel diseases by disrupting NF-κB and mTORC1 pathways · Genes and Diseases · 2026 · Same journal
• Xbp1s regulates cardiac fibrosis by transcriptionally activating Stat3 in mice · Genes and Diseases · 2026 · Same journal
• Loss of CCDC3 alleviates MAFLD and metabolic aging of mice through enhanced AGXT-associated hepatocyte glycine metabolism · Genes and Diseases · 2026 · Same journal
• Enhancer/HMGCS1 axis-mediated lipid metabolism remodeling promotes TAM resistance in ER+ breast cancer · Genes and Diseases · 2026 · Same journal
• Integrative genetic and transcriptomic analyses reveal alternative carcinogenetic pathways in basal cell carcinoma · Genes and Diseases · 2026 · Same journal
• Immune cell-derived exosomes in autoimmune diseases: From pathogenic mechanisms to innovative therapeutics · Genes and Diseases · 2026 · Same journal
• Activation of the cGAS–STING pathway mediated by IRGM1 contributes to the development of restrictive cardiomyopathy induced by cTnIR193H mutation · Genes and Diseases · 2026 · Same journal