1. Yu, Tian-Jian, Liu, Ying-Ying, Li, Xiao-Guang, Di, Gen-Hong, Jiang, Yi-Zhou. 2021. PDSS1-Mediated Activation of CAMK2A-STAT3 Signaling Promotes Metastasis in Triple-Negative Breast Cancer. In Cancer research, 81, 5491-5505. doi:10.1158/0008-5472.CAN-21-0747. https://pubmed.ncbi.nlm.nih.gov/34408002/
2. Münch, Juliane, Prasuhn, Jannik, Laugwitz, Lucia, Klee, Dirk, Distelmaier, Felix. 2023. Neuroimaging in Primary Coenzyme-Q10-Deficiency Disorders. In Antioxidants (Basel, Switzerland), 12, . doi:10.3390/antiox12030718. https://pubmed.ncbi.nlm.nih.gov/36978966/
3. Yang, Yuping, Li, Jinying, Tang, Ming, Nie, Biao, Huang, Wei. 2022. Decaprenyl Diphosphate Synthase Subunit 1 (PDSS1): A Potential Prognostic Biomarker and Immunotherapy-Target for Hepatocellular Carcinoma. In Cancer management and research, 14, 1627-1639. doi:10.2147/CMAR.S364346. https://pubmed.ncbi.nlm.nih.gov/35535267/
4. Habib, Clair, Tal, Galit, Weiss, Karin, Magen, Daniella, Pollack, Shirley. 2024. PDSS1 mutations-associated steroid-resistant nephrotic syndrome: case report and review of literature. In Pediatric nephrology (Berlin, Germany), , . doi:10.1007/s00467-024-06596-y. https://pubmed.ncbi.nlm.nih.gov/39656276/
5. Nardecchia, Francesca, De Giorgi, Agnese, Palombo, Flavia, Caporali, Leonardo, Leuzzi, Vincenzo. 2020. Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafness. In Annals of clinical and translational neurology, 8, 247-251. doi:10.1002/acn3.51232. https://pubmed.ncbi.nlm.nih.gov/33285023/
6. Lin, Kainan, Cai, Jingwei, Pan, Siyuan, Li, Qinglin, Jin, Renan. 2024. Screening of PDSS1 as a Potential Biomarker for Hepatocellular Carcinoma Based on a Copper-Related Prognostic Signature through Bulk and Single-cell RNA-sequencing Analysis. In Journal of Cancer, 15, 5028-5045. doi:10.7150/jca.96867. https://pubmed.ncbi.nlm.nih.gov/39132167/
7. Bellusci, Marcello, García-Silva, Maria Teresa, Martínez de Aragón, Ana, Martín, Miguel Angel. 2021. Distal phalangeal erythema in an infant with biallelic PDSS1 mutations: Expanding the phenotype of primary Coenzyme Q10 deficiency. In JIMD reports, 62, 3-5. doi:10.1002/jmd2.12216. https://pubmed.ncbi.nlm.nih.gov/34765390/
8. Jurkute, Neringa, Cancellieri, Francesca, Pohl, Lisa, Webster, Andrew R, Arno, Gavin. 2022. Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype. In NPJ genomic medicine, 7, 60. doi:10.1038/s41525-022-00330-z. https://pubmed.ncbi.nlm.nih.gov/36266294/
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