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

sgRNA amount is a limiting factor in adenine base editing using RNA LNPs

sgRNA 的量是利用 RNA LNP 进行腺嘌呤碱基编辑的限制因素。

Birkenshaw, Alexandra; Thomson, Tyler; Truong, Mai P; Komaki, Yui; Ramsden, Nadine; Timpano, Ana; Huang, Cassie; Blakney, Anna K; Kurek, Daniel Z; Kulkarni, Jayesh; Ross, Colin J D

Pathway-Informed Machine Learning Identifies Genetic Predictors of High-Dose Methotrexate-Induced Mucositis in Pediatric Acute Lymphoblastic Leukemia

基于通路信息的机器学习识别高剂量甲氨蝶呤诱导的儿童急性淋巴细胞白血病黏膜炎的遗传预测因子

Zhang, Xiao Yu Cindy; Scott, Erika N; Maagdenberg, Hedy; Man, Alice; Li, Kathy H; Rassekh, S Rod; Carleton, Bruce C; Ross, Colin J D; Wasserman, Wyeth W; Loucks, Catrina M

Development and Validation of a Novel Prediction Model for Hearing Loss From Cisplatin Chemotherapy

顺铂化疗引起听力损失的新型预测模型的开发与验证

Millstein, Joshua; Rassekh, Shahrad R; Brown, Austin L; Nie, Qi; Esbenshade, Adam J; Knight, Kristin R; Scheurer, Michael E; Sung, Lillian; Brooks, Beth; Moke, Diana J; Ross, Colin J D; Wright, Michael; Mena, Victoria; Rushing, Teresa; Carleton, Bruce C; Orgel, Etan

Transfection Potency of Lipid Nanoparticles Containing mRNA Depends on Relative Loading Levels

含mRNA脂质纳米粒子的转染效率取决于相对载量水平

Liao, Suiyang; Wang, Shuangyu; Wadhwa, Abishek; Birkenshaw, Alexandra; Fox, Kevin; Cheng, Miffy Hok Yan; Casmil, Irafasha C; Magana, Armando Alcazar; Bathula, Nuthan Vikas; Ho, Chia Hao; Cheng, Jin-Yu; Foster, Leonard J; Harder, Kenneth W; Ross, Colin J D; Cullis, Pieter R; Blakney, Anna K

SCN3A-related neurodevelopmental disorder: Clinical case reports and biophysical characterization

SCN3A相关神经发育障碍:临床病例报告和生物物理特征

Ghovanloo, Mohammad-Reza; Gershome, Cynthia; van der Lee, Robin; Drogemoller, Britt; Zhang, Linhua; Matthews, Allison; Blydt-Hansen, Ingrid; Nikkel, Sarah M; Demos, Michelle; Wasserman, Wyeth W; Ross, Colin J; van Karnebeek, Clara D; Ruben, Peter C

Four Pharmacogenomic Variants Strongly Linked to Corticosteroid-Induced Avascular Necrosis in Children with Cancer

四种药物基因组学变异与儿童癌症患者皮质类固醇诱导的无血管性坏死密切相关

Cordova-Delgado, Miguel; Scott, Erika N; Rassekh, Shahrad R; Loucks, Catrina M; Chang, Wan-Chun; Raack, Edward J; Trueman, Jessica N; Ross, Colin J D; Carleton, Bruce C

Human germline biallelic loss-of-function OSMR variants cause severe allergic disease

人类生殖系双等位基因功能缺失的OSMR变异会导致严重的过敏性疾病

Sharma, Mehul; Samra, Simran; Liu, Yihui; James, Alyssa; Michalski, Christina; Yousefi, Pariya; Del Bel, Kate L; Lu, Henry Y; Sharma, Ashish A; Tarailo-Graovac, Maja; Dalmann, Joshua; Buder, Lily; Modi, Bhavi; Drogemoller, Britt; Blanchard Rohner, Géraldine; Senger, Christof; Rehmus, Wingfield; Prendiville, Julie S; Mangino, Massimo; Ross, Colin J; van Karnebeek, Clara Dm; Wasserman, Wyeth W; Lavoie, Pascal M; Prathibha, P M; Biggs, Catherine M; Boehnke, Michael; Kinnunen, Leena; Koistinen, Heikki A; McKinnon, Margaret L; Patil, Siddaramappa Jagdish; Bayer, Diana K; Lyons, Jonathan J; Turvey, Stuart E

CIAO1 and MMS19 deficiency: A lethal neurodegenerative phenotype caused by cytosolic Fe-S cluster protein assembly disorders

CIAO1 和 MMS19 缺陷:由胞质铁硫簇蛋白组装障碍引起的致命性神经退行性表型

van Karnebeek, Clara D M; Tarailo-Graovac, Maja; Leen, René; Meinsma, Rutger; Correard, Solenne; Jansen-Meijer, Judith; Prykhozhij, Sergey V; Pena, Izabella A; Ban, Kevin; Schock, Sarah; Saxena, Vishal; Pras-Raves, Mia L; Drögemöller, Britt I; Grootemaat, Anita E; van der Wel, Nicole N; Dobritzsch, Doreen; Roseboom, Winfried; Schomakers, Bauke V; Jaspers, Yorrick R J; Zoetekouw, Lida; Roelofsen, Jeroen; Ferreira, Carlos R; van der Lee, Robin; Ross, Colin J; Kochan, Jakub; McIntyre, Rebecca L; van Klinken, Jan B; van Weeghel, Michel; Kramer, Gertjan; Weschke, Bernhard; Labrune, Philippe; Willemsen, Michèl A; Riva, Daria; Garavaglia, Barbara; Moeschler, John B; Filiano, James J; Ekker, Marc; Berman, Jason N; Dyment, David; Vaz, Frédéric M; Wasserman, Wyeth W; Houtkooper, Riekelt H; van Kuilenburg, André B P

Genomic variations associated with risk and protection against vincristine-induced peripheral neuropathy in pediatric cancer patients

儿童癌症患者中与长春新碱诱导周围神经病变风险和保护作用相关的基因组变异

Mufti, Kheireddin; Cordova, Miguel; Scott, Erika N; Trueman, Jessica N; Lovnicki, Jessica M; Loucks, Catrina M; Rassekh, Shahrad R; Ross, Colin J D; Carleton, Bruce C

Empowerment in Adolescent Patients with a Disability/Chronic Condition: A Scoping Review

赋能残疾/慢性病青少年患者:范围界定综述

Austin, Kennedy; Pistawka, Carly; Ross, Colin J D; Selby, Kathryn A; Virani, Alice; Kitchin, Vanessa; Elliott, Alison M