Dock6-flox 基因敲除小鼠

1. Nieto-Benito, Lula Maria, Suárez-Fernández, Ricardo, Campos-Domínguez, Minia. 2023. A novel pathogenic variation of DOCK6 gene: the genotype-phenotype correlation in Adams-Oliver syndrome. In Molecular biology reports, 50, 5519-5521. doi:10.1007/s11033-023-08430-4. https://pubmed.ncbi.nlm.nih.gov/37133614/

2. Alzahem, Tariq, Alsalamah, Abrar K, Mura, Marco, Alsulaiman, Sulaiman M. 2020. A novel variant in DOCK6 gene associated with Adams-Oliver syndrome type 2. In Ophthalmic genetics, 41, 377-380. doi:10.1080/13816810.2020.1776339. https://pubmed.ncbi.nlm.nih.gov/32498638/

3. Dessay, Mariam, Couture, Emile, Maaroufi, Halim, Brown, Jacques P, Michou, Laëtitia. 2022. Attenuated clinical and osteoclastic phenotypes of Paget's disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 gene. In BMC medical genomics, 15, 41. doi:10.1186/s12920-022-01198-9. https://pubmed.ncbi.nlm.nih.gov/35241069/

4. Hong, Kai, Cen, Kenan, Chen, Qiaoqiao, Mai, Yifeng, Guo, Yangyang. 2023. Identification and validation of a novel senescence-related biomarker for thyroid cancer to predict the prognosis and immunotherapy. In Frontiers in immunology, 14, 1128390. doi:10.3389/fimmu.2023.1128390. https://pubmed.ncbi.nlm.nih.gov/36761753/

5. Saygin, Didem, Tabib, Tracy, Bittar, Humberto E T, Rojas, Mauricio, Lafyatis, Robert. 2020. Transcriptional profiling of lung cell populations in idiopathic pulmonary arterial hypertension. In Pulmonary circulation, 10, . doi:10.1177/2045894020908782. https://pubmed.ncbi.nlm.nih.gov/32166015/

6. Cerikan, Berati, Schiebel, Elmar. 2017. Mechanism of cell-intrinsic adaptation to Adams-Oliver Syndrome gene DOCK6 disruption highlights ubiquitin-like modifier ISG15 as a regulator of RHO GTPases. In Small GTPases, 10, 210-217. doi:10.1080/21541248.2017.1297882. https://pubmed.ncbi.nlm.nih.gov/28287327/

7. Zhang, Kaihui, Gao, Zaifen, Jin, Ruifeng, Gai, Zhongtao, Liu, Yi. . [Analysis of DOCK6 gene mutation in a child affected with Adams-Oliver syndrome type 2]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 36, 348-351. doi:10.3760/cma.j.issn.1003-9406.2019.04.014. https://pubmed.ncbi.nlm.nih.gov/30950023/

8. Wang, Zhaokun, Wang, Xin, Tang, Xia. 2019. Novel compound heterozygous mutations of the DOCK6 gene in a familial case of Adams-Oliver syndrome 2. In Gene, 700, 65-69. doi:10.1016/j.gene.2019.03.023. https://pubmed.ncbi.nlm.nih.gov/30898718/

9. Sukalo, Maja, Tilsen, Felix, Kayserili, Hülya, Southgate, Laura, Zenker, Martin. 2015. DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies. In Human mutation, 36, 593-8. doi:10.1002/humu.22795. https://pubmed.ncbi.nlm.nih.gov/25824905/