1. Rondou, Pieter, Skieterska, Kamila, Packeu, Ann, Haegeman, Guy, Van Craenenbroeck, Kathleen. 2010. KLHL12-mediated ubiquitination of the dopamine D4 receptor does not target the receptor for degradation. In Cellular signalling, 22, 900-13. doi:10.1016/j.cellsig.2010.01.014. https://pubmed.ncbi.nlm.nih.gov/20100572/
2. Patalano, Susan, Rodríguez-Nieves, José, Colaneri, Cory, Riley, Todd, Macoska, Jill. 2018. CXCL12/CXCR4-Mediated Procollagen Secretion Is Coupled To Cullin-RING Ubiquitin Ligase Activation. In Scientific reports, 8, 3499. doi:10.1038/s41598-018-21506-7. https://pubmed.ncbi.nlm.nih.gov/29472636/
3. Rondou, Pieter, Haegeman, Guy, Vanhoenacker, Peter, Van Craenenbroeck, Kathleen. 2008. BTB Protein KLHL12 targets the dopamine D4 receptor for ubiquitination by a Cul3-based E3 ligase. In The Journal of biological chemistry, 283, 11083-96. doi:10.1074/jbc.M708473200. https://pubmed.ncbi.nlm.nih.gov/18303015/
4. Santangelo, Alessandra, Rossato, Marzia, Lombardi, Giuseppe, Zagonel, Vittorina, Cabrini, Giulio. . A molecular signature associated with prolonged survival in glioblastoma patients treated with regorafenib. In Neuro-oncology, 23, 264-276. doi:10.1093/neuonc/noaa156. https://pubmed.ncbi.nlm.nih.gov/32661549/
5. Funato, Yosuke, Terabayashi, Takeshi, Sakamoto, Reiko, Yoshida, Nobuaki, Miki, Hiroaki. 2010. Nucleoredoxin sustains Wnt/β-catenin signaling by retaining a pool of inactive dishevelled protein. In Current biology : CB, 20, 1945-52. doi:10.1016/j.cub.2010.09.065. https://pubmed.ncbi.nlm.nih.gov/20970343/
6. Uchida, Kazuo, Akita, Yoichi, Matsuo, Keitaro, Shimozato, Kazuo, Kozaki, Ken-Ichi. . Identification of specific autoantigens in Sjögren's syndrome by SEREX. In Immunology, 116, 53-63. doi:. https://pubmed.ncbi.nlm.nih.gov/16108817/
7. Miolo, Gianmaria, Giuffrida, Maria Grazia, Corona, Giuseppe, Tessitori, Giovanni, Bernardini, Laura. 2018. A novel mosaic 1q32.1 microduplication identified through Chromosome Microarray Analysis: narrowing the smallest critical region including KDM5B gene found associated with neurodevelopmetal disorders. In European journal of medical genetics, 62, 103558. doi:10.1016/j.ejmg.2018.10.010. https://pubmed.ncbi.nlm.nih.gov/31405577/
8. Ma, Dexuan, Yang, Jingyun, Wang, Ying, Du, Guhong, Zhou, Liangfu. 2017. Whole exome sequencing identified genetic variations in Chinese hemangioblastoma patients. In American journal of medical genetics. Part A, 173, 2605-2613. doi:10.1002/ajmg.a.38350. https://pubmed.ncbi.nlm.nih.gov/28742274/
智鼠故事 
