Hadhb-KO 基因敲除小鼠

1. Dagher, Robin, Massie, Rami, Gentil, Benoit J. 2021. MTP deficiency caused by HADHB mutations: Pathophysiology and clinical manifestations. In Molecular genetics and metabolism, 133, 1-7. doi:10.1016/j.ymgme.2021.03.010. https://pubmed.ncbi.nlm.nih.gov/33744096/

2. Wang, Wan-Li, Jiang, Hong-Jie, Shen, Ze-Liang, Jiang, Jian, Liang, Xin-Hua. 2024. Identification of ACAA1 and HADHB as potential prognostic biomarkers based on a novel fatty acid oxidation-related gene model in head and neck squamous cell carcinoma: A retrospective study. In Archives of oral biology, 163, 105982. doi:10.1016/j.archoralbio.2024.105982. https://pubmed.ncbi.nlm.nih.gov/38678878/

3. Diebold, Isabel, Schön, Ulrike, Horvath, Rita, Kölbel, Heike, Abicht, Angela. 2019. HADHA and HADHB gene associated phenotypes - Identification of rare variants in a patient cohort by Next Generation Sequencing. In Molecular and cellular probes, 44, 14-20. doi:10.1016/j.mcp.2019.01.003. https://pubmed.ncbi.nlm.nih.gov/30682426/

4. Lu, Minjun, Li, Wenxin, Zhou, Jiamin, Liu, Yueqin, Zhu, Xiaolan. 2024. Integrative bioinformatics analysis for identifying the mitochondrial-related gene signature associated with immune infiltration in premature ovarian insufficiency. In BMC medicine, 22, 444. doi:10.1186/s12916-024-03675-7. https://pubmed.ncbi.nlm.nih.gov/39379953/