MOL THER-METH CLIN D 润色咨询

Molecular Therapy-Methods & Clinical Development

出版年份:暂无数据 年文章数:1026 投稿命中率: 开通期刊会员,数据随心看

出版周期:Irregular 自引率:5.4% 审稿周期: 开通期刊会员,数据随心看

前往期刊查询

投稿信息

投稿信息
审稿费用
暂无数据
版面费用
暂无数据
中国人发表比例
2023年中国人文章占该期刊总数量暂无数据 (2022年为100.00%)
自引率
5.4 %
年文章数
1026
期刊官网
点击查看 (点击次数:2929)
点击查看 (点击次数:1269次)
作者需知
点击查看 (点击次数:810次)
偏重的研究方向
暂无数据
期刊简介
稿件收录要求

Molecular Therapy

Molecular Therapy is the leading journal for research in the areas of gene transfer, vector development and design, stem cell manipulation, development of gene-, peptide-, protein-, oligonucleotide-, and cell-based therapeutics to correct genetic and acquired diseases, vaccine development, pre-clinical target validation, safety/efficacy studies, and clinical trials. Molecular Therapy is dedicated to promoting the sciences in genetics, medicine, and biotechnology. Publishing important peer-reviewed research and cutting-edge reviews and commentaries, the journal continues to attract the best material in the field. Molecular Therapy''s 2015 impact factor is 6.938.

Molecular Therapy — Methods & Clinical Developments

The aim of Molecular Therapy—Methods & Clinical Development is to build upon the success of Molecular Therapy in publishing important peer-reviewed methods and procedures, as well as translational advances in the broad array of fields under the molecular therapy umbrella.

Topics of particular interest within the journal''s scope include:

  • Gene vector engineering and production
  • Methods for targeted genome editing and engineering
  • Methods and technology development for cell reprogramming and directed differentiation of pluripotent cells
  • Methods for gene and cell vector delivery
  • Development of biomaterials and nanoparticles for applications in gene and cell therapy and regenerative medicine
  • Analysis of gene and cell vector biodistribution and tracking
  • Pharmacology/toxicology studies of new and next-generation vectors
  • Methods for cell isolation, engineering, culture, expansion, and transplantation
  • Cell processing, storage, and banking for therapeutic application
  • Preclinical and QC/QA assay development
  • Translational and clinical scale-up and Good Manufacturing procedures and process development
  • Clinical protocol development
  • Computational and bioinformatic methods for analysis, modeling, or visualization of biological data
  • Negotiating the regulatory approval process and obtaining such approval for clinical trials