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Titlebook: Recent Trends in Electronics and Communication; Select Proceedings o Amit Dhawan,Vijay Shanker Tripathi,Kshirasagar Nai Conference proceedi

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11#
發(fā)表于 2025-3-23 11:58:01 | 只看該作者
12#
發(fā)表于 2025-3-23 15:59:53 | 只看該作者
Akash Gaikwad,Sukwinder Singhny?mutations that potentially lead to exon skipping. To functionally test these?a lot can be achieved with a limited set of protocols, while for the intentional induction of exon skipping different tools and target genes are involved and the translational path from .in vitro. splicing to .in vivo. t
13#
發(fā)表于 2025-3-23 20:11:00 | 只看該作者
Ritesh Kumar Kushwaha,P. Karuppanan,Nand Kishoreny?mutations that potentially lead to exon skipping. To functionally test these?a lot can be achieved with a limited set of protocols, while for the intentional induction of exon skipping different tools and target genes are involved and the translational path from .in vitro. splicing to .in vivo. t
14#
發(fā)表于 2025-3-23 23:03:28 | 只看該作者
15#
發(fā)表于 2025-3-24 02:24:12 | 只看該作者
Monica Khanore,Srija Unnikrishnanmentation advice from the experts.Includes supplementary mat.“Next generation” sequencing techniques allow for more detailed analysis of exons and introns in multiple genes at the same time. This will reveal many?mutations that potentially lead to exon skipping. To functionally test these?a lot can
16#
發(fā)表于 2025-3-24 09:10:25 | 只看該作者
Vipin Verma,Sarika Pal,Narendra Pal,Dharmendra Kumarny?mutations that potentially lead to exon skipping. To functionally test these?a lot can be achieved with a limited set of protocols, while for the intentional induction of exon skipping different tools and target genes are involved and the translational path from .in vitro. splicing to .in vivo. t
17#
發(fā)表于 2025-3-24 12:57:20 | 只看該作者
18#
發(fā)表于 2025-3-24 17:10:05 | 只看該作者
19#
發(fā)表于 2025-3-24 19:09:08 | 只看該作者
20#
發(fā)表于 2025-3-24 23:26:40 | 只看該作者
Abhinav Gupta,Vikrant Varshney,Adarsh Vishwakarma,Arunabh Kishore,Atul Pal,Piyush Mishra,Varnika Patcular dystrophy patients, it has been established that AONs sharing similar chemistry have clear clinical potential. Genetic diseases, such as facioscapulohumeral dystrophy (FSHD), can be the result of gain-of-function mutations. Since mRNA processing in terms of termination of transcription, its tr
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