日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A new dystrophin-deficient rat model mirroring exon skipping in patients with DMD exon 45 deletions

一种新的肌营养不良蛋白缺陷大鼠模型,模拟了DMD患者45号外显子缺失中的外显子跳跃现象

Wang, Tao; Daoud, Cynthia; Dubois, Auriane; Corre, Guillaume; Bellec, Jessica; Bovolenta, Matteo; Philidet, Louise; Dorval, Alan; Bourg, Nathalie; Roudaut, Carinne; Albini, Sonia; Warthi, Ganesh; Jaber, Abbass; Richard, Isabelle

Correction of exon 2, exon 2-9 and exons 8-9 duplications in DMD patient myogenic cells by a single CRISPR/Cas9 system

通过单个 CRISPR/Cas9 系统纠正 DMD 患者成肌细胞中的外显子 2、外显子 2-9 和外显子 8-9 重复

Juliette Lemoine, Auriane Dubois, Alan Dorval, Abbass Jaber, Ganesh Warthi, Kamel Mamchaoui, Tao Wang, Guillaume Corre, Matteo Bovolenta #, Isabelle Richard #

INKILN is a Novel Long Noncoding RNA Promoting Vascular Smooth Muscle Inflammation via Scaffolding MKL1 and USP10

INKILN是一种新型长链非编码RNA,可通过支架蛋白MKL1和USP10促进血管平滑肌炎症。

Zhang, Wei; Zhao, Jinjing; Deng, Lin; Ishimwe, Nestor; Pauli, Jessica; Wu, Wen; Shan, Shengshuai; Kempf, Wolfgang; Ballantyne, Margaret D; Kim, David; Lyu, Qing; Bennett, Matthew; Rodor, Julie; Turner, Adam W; Lu, Yao Wei; Gao, Ping; Choi, Mihyun; Warthi, Ganesh; Kim, Ha Won; Barroso, Margarida M; Bryant, William B; Miller, Clint L; Weintraub, Neal L; Maegdefessel, Lars; Miano, Joseph M; Baker, Andrew H; Long, Xiaochun

Generation and Comparative Analysis of an Itga8-CreER T2 Mouse with Preferential Activity in Vascular Smooth Muscle Cells

具有血管平滑肌细胞优先活性的 Itga8-CreER T2 小鼠的生成和比较分析

Ganesh Warthi, Jessica L Faulkner, Jaser Doja, Amr R Ghanam, Pan Gao, Allison C Yang, Orazio J Slivano, Candee T Barris, Taylor C Kress, Scott D Zawieja, Susan H Griffin, Xiaoling Xie, Alan Ashworth, Christine K Christie, William B Bryant, Ajay Kumar, Michael J Davis, Xiaochun Long, Lin Gan, Eric J

Systematic Nucleotide Exchange Analysis of ESTs From the Human Cancer Genome Project Report: Origins of 347 Unknown ESTs Indicate Putative Transcription of Non-Coding Genomic Regions

人类癌症基因组计划报告中EST的系统性核苷酸交换分析:347个未知EST的起源表明非编码基因组区域可能存在转录

Warthi, Ganesh; Fournier, Pierre-Edouard; Seligmann, Hervé

Chimeric Translation for Mitochondrial Peptides: Regular and Expanded Codons

线粒体肽的嵌合翻译:常规和扩展密码子

Hervé Seligmann, Ganesh Warthi

Transcripts with systematic nucleotide deletion of 1-12 nucleotide in human mitochondrion suggest potential non-canonical transcription

人类线粒体中系统性缺失1-12个核苷酸的转录本提示可能存在非经典转录途径。

Warthi, Ganesh; Seligmann, Hervé

Genetic Code Optimization for Cotranslational Protein Folding: Codon Directional Asymmetry Correlates with Antiparallel Betasheets, tRNA Synthetase Classes

共翻译蛋白质折叠的遗传密码优化:密码子方向不对称性与反平行β折叠、tRNA合成酶类别相关

Seligmann, Hervé; Warthi, Ganesh