Cabp2-flox 基因敲除小鼠

1. Koohiyan, Mahbobeh, Noori-Daloii, Mohammad Reza, Hashemzadeh-Chaleshtori, Morteza, Abtahi, Hamidreza, Tabatabaiefar, Mohammad Amin. 2019. A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family. In Audiology & neuro-otology, 24, 258-263. doi:10.1159/000502251. https://pubmed.ncbi.nlm.nih.gov/31661684/

2. Bharadwaj, Thashi, Schrauwen, Isabelle, Acharya, Anushree, Kotimäki, Jouko, Leal, Suzanne M. 2022. Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant. In Molecular genetics & genomic medicine, 10, e1866. doi:10.1002/mgg3.1866. https://pubmed.ncbi.nlm.nih.gov/35150090/

3. Oestreicher, David, Chepurwar, Shashank, Kusch, Kathrin, Strenzke, Nicola, Pangrsic, Tina. 2024. CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells. In eLife, 13, . doi:10.7554/eLife.93646. https://pubmed.ncbi.nlm.nih.gov/39718549/

4. Safka Brozkova, Dana, Poisson Marková, Simona, Mészárosová, Anna Uhrová, Rašková, Dagmar, Seeman, Pavel. 2020. Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing. In Clinical genetics, 98, 548-554. doi:10.1111/cge.13839. https://pubmed.ncbi.nlm.nih.gov/32860223/