Tti2-KO 基因敲除小鼠

1. Senko, Anna N, Overall, Rupert W, Silhavy, Jan, Pravenec, Michal, Kempermann, Gerd. 2022. Systems genetics in the rat HXB/BXH family identifies Tti2 as a pleiotropic quantitative trait gene for adult hippocampal neurogenesis and serum glucose. In PLoS genetics, 18, e1009638. doi:10.1371/journal.pgen.1009638. https://pubmed.ncbi.nlm.nih.gov/35377872/

2. Garcia, Nelson, Li, Yubin, Dooner, Hugo K, Messing, Joachim. 2017. Maize defective kernel mutant generated by insertion of a Ds element in a gene encoding a highly conserved TTI2 cochaperone. In Proceedings of the National Academy of Sciences of the United States of America, 114, 5165-5170. doi:10.1073/pnas.1703498114. https://pubmed.ncbi.nlm.nih.gov/28461460/

3. Serey-Gaut, Margaux, Cortes, Marisol, Makrythanasis, Periklis, Dawson, Ted M, Antonarakis, Stylianos E. 2023. Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly. In American journal of human genetics, 110, 499-515. doi:10.1016/j.ajhg.2023.01.006. https://pubmed.ncbi.nlm.nih.gov/36724785/

4. Ziegler, Alban, Bader, Patricia, McWalter, Kirsty, Colin, Estelle, Bonneau, Dominique. 2019. Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disability. In Clinical genetics, 96, 354-358. doi:10.1111/cge.13603. https://pubmed.ncbi.nlm.nih.gov/31290144/

5. Hoffman, Kyle S, Duennwald, Martin L, Karagiannis, Jim, McCarton, Alexander S, Brandl, Christopher J. 2016. Saccharomyces cerevisiae Tti2 Regulates PIKK Proteins and Stress Response. In G3 (Bethesda, Md.), 6, 1649-59. doi:10.1534/g3.116.029520. https://pubmed.ncbi.nlm.nih.gov/27172216/

6. Qarnain, Zul, Khan, Fatima, Akbar, Fizza, Kirmani, Salman. 2022. Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report). In Case reports in genetics, 2022, 2766957. doi:10.1155/2022/2766957. https://pubmed.ncbi.nlm.nih.gov/35990009/

7. Picher-Martel, Vincent, Labrie, Yvan, Rivest, Serge, Lace, Baiba, Chrestian, Nicolas. 2020. Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report. In BMC neurology, 20, 58. doi:10.1186/s12883-020-01643-1. https://pubmed.ncbi.nlm.nih.gov/32061250/

8. Langouët, Maéva, Saadi, Abdelkrim, Rieunier, Guillaume, Chaouch, Malika, Colleaux, Laurence. 2013. Mutation in TTI2 reveals a role for triple T complex in human brain development. In Human mutation, 34, 1472-6. doi:10.1002/humu.22399. https://pubmed.ncbi.nlm.nih.gov/23956177/

9. Genereaux, Julie, Kvas, Stephanie, Dobransky, Dominik, Gloor, Gregory B, Brandl, Christopher J. 2012. Genetic evidence links the ASTRA protein chaperone component Tti2 to the SAGA transcription factor Tra1. In Genetics, 191, 765-80. doi:10.1534/genetics.112.140459. https://pubmed.ncbi.nlm.nih.gov/22505622/

10. Inoue, Haruna, Sugimoto, Shizuka, Takeshita, Yumiko, Yanagida, Mitsuhiro, Kanoh, Junko. 2016. CK2 phospho-independent assembly of the Tel2-associated stress-signaling complexes in Schizosaccharomyces pombe. In Genes to cells : devoted to molecular & cellular mechanisms, 22, 59-70. doi:10.1111/gtc.12454. https://pubmed.ncbi.nlm.nih.gov/27935167/