Searching journal content for articles similar to Wang et al. 27 (12): 2061.

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  1. ...Corrigendum: Cre-dependent Cas9-expressing pigs enable efficient in vivo editing Kepin Wang, Qin Jin, Degong Ruan, Yi Yang, Qishuai Liu, Han Wu, Zhiwei Zhou, Zhen Ouyang, Zhaoming Liu, Yu Zhao, Bentian Zhao, Quanjun Zhang, Jiangyun Peng, Chengdan Lai, Nana Fan, Yanhui Liang, Ting Lan, Nan Li...
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  2. ...these markers with green fluorescent protein (GFP) in 238 the sgRNA–Cas9 expression constructs (Supplemental Fig. S4A–C). The detection of 239 transient GFP expression enabled the rapid and non-toxic isolation of transfected cells 240 by FACS, which allows for precision gating based on fluorescence intensity...
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  3. ...editing efficiency. This approach led to the successful generation of xenotransplantation pigs with multiple homozygously edited genes in a much shorter time frame than previously achievable.ResultsSurrogate reporters for genomic targetingEfficient selection methods are essential for enhancing multiplex...
  4. ...).PCRs on genomic DNA from the cells that completed MAC development were used to check whether the ICOP KDs affect IES excision (Fig. 4C). Longer fragments containing IESs (IES+) were amplified in all KD permutations, suggesting ICOPs are essential during editing.Next, we investigated the -wide effect of ICOP KDs...
  5. ...To comprehensively profile alternative polyadenylation across pig tissues, we analyzed 10x Genomics single-nucleus RNA sequencing (10x snRNA-seq) data from our previous study as a preprint on bioRxiv (Chen et al. 2023), which identified 261 cell subtypes spanning 19 distinct pig tissues (Supplemental Table S1...
  6. .... Science (1979) 309: 1564–1566. doi:10.1126/science.1112009 Katrekar D, Yen J, Xiang Y, Saha A, Meluzzi D, Savva Y, Mali P. 2022. Efficient in vitro and in vivo RNA editing via recruitment of endogenous ADARs using circular guide RNAs. Nat Biotechnol 40: 938–945. doi:10 .1038/s41587-021-01171-4 Kim DDY...
  7. ...consumption, while41 reducing the sensitivity of decomposition results to parameter settings. These improvements enable more robust,42 accurate, and efficient analysis of TR reads and assemblies.43 1 1 1 1 AA A T T A A A Input Output AA A T T A A A Tandem Repeat Sequence: R AA A TT T STRs LTRs Template...
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  8. ...six different genomic deletions spanning RE1–3 (Supplemental Fig. S48B) or sgRNAs for mCherry or EGFP as controls. The Cas9 protein was equally expressed from all vectors in C1 cells compared with GAPDH (Supplemental Fig. S48C). After 2 days of puromycin selection for Cas9-expressing C1 cells, we...
  9. ...the transcriptome (Eisenberg and Levanon 2018; Duan 2025). Editing events taking place in coding sequences (CDSs)might alter the genomically encoded amino acid and lead to nonsynonymous changes, namely, “recoding” (Alon et al. 2015). Genome-wide profiling of RNA editing sites has been performed in several metazoans...
  10. ...for graphs. Bioinformatics 37: i460–i467. doi:10.1093/bioinformatics/btab302 ↵Letcher B, Hunt M, Iqbal Z. 2021. Gramtools enables multiscale variation analysis with graphs. Genome Biol 22: 259. doi:10.1186/s13059-021-02474-0 ↵Li H. 2022. Sample graphs and sequences for testing sequence-to-graph alignment...
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