Spinal-Fusion 发表于 2025-3-27 00:07:20
https://doi.org/10.1007/978-1-349-20987-3 gene function via tissue- or cell-specific mutagenesis remains challenging in zebrafish when the study of the function of certain loci might require tight spatiotemporal control of gene inactivation, which is particularly true in studying the function of a particular gene in post mitotic neurons, w终端 发表于 2025-3-27 01:51:11
https://doi.org/10.1007/978-3-8349-6807-4ogenic iPSC lines were created. We found that the disease phenotypes only manifested in the differentiated neural stem cell (NSC) stage, not in iPSCs. Transcriptomic analysis of HD iPSCs and HD NSCs compared to isogenic controls was utilized to understand the molecular basis for the CAG repeat expan或者发神韵 发表于 2025-3-27 08:05:04
http://reply.papertrans.cn/39/3829/382839/382839_33.pngSynovial-Fluid 发表于 2025-3-27 09:57:55
http://reply.papertrans.cn/39/3829/382839/382839_34.png男生戴手铐 发表于 2025-3-27 13:45:51
Determinanten der Bildungsungleichheitrated transgenic marmosets with germ line transmission, opening new avenues in primate research..In this chapter, we describe recent advances in neuroscience and disease research using common marmosets, and we outline potential uses of genome editing in non-human primates toward the development of knock-in/knock-out marmosets.剧本 发表于 2025-3-27 18:15:53
,Grundzüge der Kapitalstrukturtheorie,g or mutation-adjacent . exons are intentionally removed in order to restore protein reading frame, and thereby Dystrophin expression, in DMD patients (Beroud et al. Hum Mutat 28:196–202, 2007; Yokota et al. Expert Opin Biol Ther 7:831–842, 2007).Insensate 发表于 2025-3-28 01:36:58
Dissecting the Role of Synaptic Proteins with CRISPR,chnique in addition to previous genetic approaches vastly simplifies and accelerates the study of specific synaptic proteins. Here we illustrate different ways that CRISPR/Cas9 can be used in the study of synaptic properties.harmony 发表于 2025-3-28 05:55:34
http://reply.papertrans.cn/39/3829/382839/382839_38.pngAPEX 发表于 2025-3-28 08:15:31
Therapeutic Gene Editing in Muscles and Muscle Stem Cells,g or mutation-adjacent . exons are intentionally removed in order to restore protein reading frame, and thereby Dystrophin expression, in DMD patients (Beroud et al. Hum Mutat 28:196–202, 2007; Yokota et al. Expert Opin Biol Ther 7:831–842, 2007).追踪 发表于 2025-3-28 12:35:14
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