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

Identification of new candidate drugs in myelodysplastic syndromes with splicing factor mutations by transcriptional profiling and connectivity map analysis

通过转录谱分析和连接图谱分析鉴定伴有剪接因子突变的骨髓增生异常综合征的新候选药物

期刊:British Journal of Haematology
影响因子:3.8
doi:10.1111/bjh.20026
Sun, Tianyu; Singh, Shalini; Wang, Hayson Chenyu; Lee, Juseong; Dolatshad, Hamid; Cheong, Pak Leng; Higgs, Douglas R; Boultwood, Jacqueline; Pellagatti, Andrea
发表日期：2025
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ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine

ASXL1 突变与导致对维奈克拉和氮杂胞苷敏感性的明显表观基因组改变有关

期刊:Blood Cancer Journal
影响因子:12.9
doi:10.1038/s41408-021-00541-0
Nora E Rahmani, Nandini Ramachandra, Srabani Sahu, Nadege Gitego, Andrea Lopez, Kith Pradhan, Tushar D Bhagat, Shanisha Gordon-Mitchell, Bianca Rivera Pena, Mohammad Kazemi, Keshav Rao, Orsi Giricz, Shahina Bano Maqbool, Raul Olea, Yongmei Zhao, Jinghang Zhang, Hamid Dolatshad, Vickram Tittrea, Dhar
信号转导
发表日期：2021
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Effects of prolactin on movement disorders and APOE, GFAP, and PRL receptor gene expression following intracerebral hemorrhage in rats

催乳素对大鼠脑出血后运动障碍及APOE、GFAP和PRL受体基因表达的影响

期刊:Iranian Journal of Basic Medical Sciences
影响因子:2.7
doi:10.22038/IJBMS.2021.58176.12927
Yousefvand, Shiba; Hadjzadeh, Mousa-Al-Reza; Keshavarzi, Zakieh; Dolatshad, Hamid; Vafaee, Farzaneh; Mahmoudabady, Maryam; Gholamzadeh Virany, Zahra
信号转导
Rat
神经科学
APOE
FAP
GFAP
发表日期：2021
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CRISPR/Cas9-mediated generation and analysis of N terminus polymorphic models of β2AR in isogenic hPSC-derived cardiomyocytes

CRISPR/Cas9 介导的同源 hPSC 衍生心肌细胞中 β2AR N 末端多态性模型的生成和分析

期刊:Molecular Therapy-Methods & Clinical Development
影响因子:
doi:10.1016/j.omtm.2020.10.019
Alexander Kondrashov, Nurul A N Mohd Yusof, Alveera Hasan, Joëlle Goulding, Thusharika Kodagoda, Duc M Hoang, Nguyen T N Vo, Tony Melarangi, Nazanin Dolatshad, Julia Gorelik, Stephen J Hill, Sian E Harding, Chris Denning
免疫
细胞生物学
其它细胞
发表日期：2020
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Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations

剪接体突变对骨髓增生异常中 RNA 剪接的影响：失调基因/通路和临床关联

期刊:Blood
影响因子:21
doi:10.1182/blood-2018-04-843771
Andrea Pellagatti, Richard N Armstrong, Violetta Steeples, Eshita Sharma, Emmanouela Repapi, Shalini Singh, Andrea Sanchi, Aleksandar Radujkovic, Patrick Horn, Hamid Dolatshad, Swagata Roy, John Broxholme, Helen Lockstone, Stephen Taylor, Aristoteles Giagounidis, Paresh Vyas, Anna Schuh, Angela Hamb
信号转导
发表日期：2018
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Clustered Regularly Interspaced Short Palindromic Repeats/Cas9 Gene Editing Technique in Xenotransplantation

异种移植中成簇规律间隔短回文重复序列/Cas9基因编辑技术

期刊:Frontiers in Immunology
影响因子:5.9
doi:10.3389/fimmu.2018.01711
Naeimi Kararoudi, Meisam; Hejazi, Seyyed S; Elmas, Ezgi; Hellström, Mats; Naeimi Kararoudi, Maryam; Padma, Arvind M; Lee, Dean; Dolatshad, Hamid
发表日期：2018
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Generation of Knock-out Primary and Expanded Human NK Cells Using Cas9 Ribonucleoproteins

利用Cas9核糖核蛋白生成基因敲除的原代和扩增的人类NK细胞

期刊:Jove-Journal of Visualized Experiments
影响因子:1
doi:10.3791/58237
Naeimi Kararoudi, Meisam; Dolatshad, Hamid; Trikha, Prashant; Hussain, Syed-Rehan A; Elmas, Ezgi; Foltz, Jennifer A; Moseman, Jena E; Thakkar, Aarohi; Nakkula, Robin J; Lamb, Margaret; Chakravarti, Nitin; McLaughlin, K John; Lee, Dean A
细胞生物学
Human
发表日期：2018
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The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes

U2AF1S34F突变导致骨髓增生异常综合征中谱系特异性剪接改变。

期刊:Journal of Clinical Investigation
影响因子:13.6
doi:10.1172/JCI96202
Yip, Bon Ham; Steeples, Violetta; Repapi, Emmanouela; Armstrong, Richard N; Llorian, Miriam; Roy, Swagata; Shaw, Jacqueline; Dolatshad, Hamid; Taylor, Stephen; Verma, Amit; Bartenstein, Matthias; Vyas, Paresh; Cross, Nicholas Cp; Malcovati, Luca; Cazzola, Mario; Hellström-Lindberg, Eva; Ogawa, Seishi; Smith, Christopher Wj; Pellagatti, Andrea; Boultwood, Jacqueline
U2AF1
发表日期：2017
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The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes

U2AF1S34F 突变可诱导骨髓增生异常综合征中的谱系特异性剪接改变

期刊:Journal of Clinical Investigation
影响因子:13.3
doi:10.1172/JCI91363
Bon Ham Yip, Violetta Steeples, Emmanouela Repapi, Richard N Armstrong, Miriam Llorian, Swagata Roy, Jacqueline Shaw, Hamid Dolatshad, Stephen Taylor, Amit Verma, Matthias Bartenstein, Paresh Vyas, Nicholas Cp Cross, Luca Malcovati, Mario Cazzola, Eva Hellström-Lindberg, Seishi Ogawa, Christopher Wj
U2AF1
发表日期：2017
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A versatile transgenic allele for mouse overexpression studies

用于小鼠过表达研究的多功能转基因等位基因

期刊:Mammalian Genome
影响因子:2.7
doi:10.1007/s00335-015-9602-y
Dolatshad, Hamid; Biggs, Daniel; Diaz, Rebeca; Hortin, Nicole; Preece, Christopher; Davies, Benjamin
发表日期：2015
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