Erc2-KO 基因敲除小鼠

1. Cheng, Peng, Chen, Kun, Zhang, Shu, Liang, Shuang, Zhang, Ying. 2021. IDH1 R132C and ERC2 L309I Mutations Contribute to the Development of Maffucci's Syndrome. In Frontiers in endocrinology, 12, 763349. doi:10.3389/fendo.2021.763349. https://pubmed.ncbi.nlm.nih.gov/34790172/

2. Seki, Shoji, Iwasaki, Mami, Makino, Hiroto, Tsuji, Mamiko, Kawaguchi, Yoshiharu. 2022. Association of Ligamentum Flavum Hypertrophy with Adolescent Idiopathic Scoliosis Progression-Comparative Microarray Gene Expression Analysis. In International journal of molecular sciences, 23, . doi:10.3390/ijms23095038. https://pubmed.ncbi.nlm.nih.gov/35563428/

3. Lam, Matti, Lee, Dylan, Kosater, Ivy, De Jager, Philip, Menon, Vilas. 2023. Human disease-specific cell signatures in non-lesional tissue in Multiple Sclerosis detected by single-cell and spatial transcriptomics. In bioRxiv : the preprint server for biology, , . doi:10.1101/2023.12.20.572491. https://pubmed.ncbi.nlm.nih.gov/38187779/

4. Jama, Maymun, Zhang, Min, Poile, Charlotte, Fennell, Dean A, Hollox, Edward J. 2023. Gene fusions during the early evolution of mesothelioma correlate with impaired DNA repair and Hippo pathways. In Genes, chromosomes & cancer, 63, e23189. doi:10.1002/gcc.23189. https://pubmed.ncbi.nlm.nih.gov/37421230/

5. Chen, Xiaotong, Liu, Lintao, Chen, Mengping, Jiang, Jinxing, Hou, Jian. 2021. A Five-Gene Risk Score Model for Predicting the Prognosis of Multiple Myeloma Patients Based on Gene Expression Profiles. In Frontiers in genetics, 12, 785330. doi:10.3389/fgene.2021.785330. https://pubmed.ncbi.nlm.nih.gov/34917133/