Scaper-flox 基因敲除小鼠

1. Kahrizi, Kimia, Huber, Mareike, Galetzka, Danuta, Najmabadi, Hossein, Winter, Jennifer. 2019. Homozygous variants in the gene SCAPER cause syndromic intellectual disability. In American journal of medical genetics. Part A, 179, 1214-1225. doi:10.1002/ajmg.a.61172. https://pubmed.ncbi.nlm.nih.gov/31069901/

2. Höpfler, Markus, Absmeier, Eva, Peak-Chew, Sew-Yeu, Gasic, Ivana, Hegde, Ramanujan S. 2023. Mechanism of ribosome-associated mRNA degradation during tubulin autoregulation. In Molecular cell, 83, 2290-2302.e13. doi:10.1016/j.molcel.2023.05.020. https://pubmed.ncbi.nlm.nih.gov/37295431/

3. Wormser, Ohad, Gradstein, Libe, Yogev, Yuval, Elia, Natalie, Birk, Ohad S. 2019. SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome. In European journal of human genetics : EJHG, 27, 928-940. doi:10.1038/s41431-019-0347-z. https://pubmed.ncbi.nlm.nih.gov/30723319/

4. Wormser, Ohad, Levy, Ygal, Bakhrat, Anna, Birk, Ohad S, Abdu, Uri. 2020. Absence of SCAPER causes male infertility in humans and Drosophila by modulating microtubule dynamics during meiosis. In Journal of medical genetics, 58, 254-263. doi:10.1136/jmedgenet-2020-106946. https://pubmed.ncbi.nlm.nih.gov/32527956/