Dchs1-flox 基因敲除小鼠

1. Miyasaka, Yuki, Kobayashi, Takeshi, Gotoh, Naoya, Kawabe, Tsutomu, Ohno, Tamio. 2022. Neonatal lethality of mouse A/J-7SM consomic strain is caused by an insertion mutation in the Dchs1 gene. In Mammalian genome : official journal of the International Mammalian Genome Society, 34, 32-43. doi:10.1007/s00335-022-09966-9. https://pubmed.ncbi.nlm.nih.gov/36434174/

2. Zhou, Nan, Zhao, Qianhao, Li, Rui, Cheng, Jianding, Chen, Yangxin. 2024. Mutation in mitral valve prolapse susceptible gene DCHS1 causes familial mitral annular disjunction. In Journal of medical genetics, 61, 125-131. doi:10.1136/jmg-2023-109278. https://pubmed.ncbi.nlm.nih.gov/37399314/

3. Durst, Ronen, Sauls, Kimberly, Peal, David S, Norris, Russell A, Slaugenhaupt, Susan A. 2015. Mutations in DCHS1 cause mitral valve prolapse. In Nature, 525, 109-13. doi:10.1038/nature14670. https://pubmed.ncbi.nlm.nih.gov/26258302/

4. Qureshi, Aslam H, Liang, Dong, Canas, Jorge, Schwaderer, Andrew L, Hains, David S. 2020. DCHS1 DNA copy number loss associated with pediatric urinary tract infection risk. In Innate immunity, 26, 473-481. doi:10.1177/1753425920917193. https://pubmed.ncbi.nlm.nih.gov/32295462/

5. Bressan, Cedric, Snapyan, Marta, Snapyan, Marina, Cappello, Silvia, Saghatelyan, Armen. 2023. Metformin rescues migratory deficits of cells derived from patients with periventricular heterotopia. In EMBO molecular medicine, 15, e16908. doi:10.15252/emmm.202216908. https://pubmed.ncbi.nlm.nih.gov/37609821/