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

Selective AMPKβ1 activation induces fetal hemoglobin in human erythroid cells and sickle cell mice via the noncanonical NRF2 pathway

选择性激活AMPKβ1可通过非经典NRF2通路诱导人红细胞和镰状细胞小鼠产生胎儿血红蛋白。

Yannis Hara ,Viktor T Lemgart ,Samuel Lessard ,Courtney J Mercadante ,Jean-Antoine Ribeil ,Alexandra Hicks ,Pauline Rimmele ,David R Light

Zinc finger nuclease-mediated gene editing in hematopoietic stem cells results in reactivation of fetal hemoglobin in sickle cell disease

锌指核酸酶介导的造血干细胞基因编辑可导致镰状细胞病中胎儿血红蛋白的重新激活

Samuel Lessard #,Pauline Rimmelé #,Hui Ling,Kevin Moran,Benjamin Vieira,Yi-Dong Lin,Gaurav Manohar Rajani,Vu Hong,Andreas Reik,Richard Boismenu,Ben Hsu,Michael Chen,Bettina M Cockroft,Naoya Uchida,John Tisdale,Asif Alavi,Lakshmanan Krishnamurti,Mehrdad Abedi,Isobelle Galeon,David Reiner,Lin Wang,Anne Ramezi,Pablo Rendo,Mark C Walters,Dana Levasseur,Robert Peters,Timothy Harris,Alexandra Hicks

A new tool for assessing short debriefings after immersive simulation: validity of the SHORT scale

一种用于评估沉浸式模拟后简短汇报的新工具:SHORT 量表的有效性

Rivière, Etienne; Aubin, Etienne; Tremblay, Samuel-Lessard; Lortie, Gilles; Chiniara, Gilles

Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci

使用多个 Cas9 核酸酶进行变异感知饱和诱变,识别性状相关基因位点的调控元件

Matthew C Canver, Samuel Lessard, Luca Pinello, Yuxuan Wu, Yann Ilboudo, Emily N Stern, Austen J Needleman, Frédéric Galactéros, Carlo Brugnara, Abdullah Kutlar, Colin McKenzie, Marvin Reid, Diane D Chen, Partha Pratim Das, Mitchel A Cole, Jing Zeng, Ryo Kurita, Yukio Nakamura, Guo-Cheng Yuan, Guill

An erythroid-specific ATP2B4 enhancer mediates red blood cell hydration and malaria susceptibility

红细胞特异性 ATP2B4 增强子介导红细胞水化和疟疾易感性

Samuel Lessard, Emily Stern Gatof, Mélissa Beaudoin, Patrick G Schupp, Falak Sher, Adnan Ali, Sukhpal Prehar, Ryo Kurita, Yukio Nakamura, Esther Baena, Jonathan Ledoux, Delvac Oceandy, Daniel E Bauer, Guillaume Lettre

Frameshift indels introduced by genome editing can lead to in-frame exon skipping

基因组编辑引入的移码插入缺失突变可导致框内外显子跳跃。

Simon Lalonde ,Oliver A Stone ,Samuel Lessard ,Adam Lavertu ,Jessica Desjardins ,Mélissa Beaudoin ,Manuel Rivas ,Didier Y R Stainier ,Guillaume Lettre