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期刊名:Molecular therapy-nucleic acids

缩写:MOL THER-NUCL ACIDS

ISSN:2162-2531

e-ISSN:2162-2531

IF/分区:6.1/Q1

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共收录本刊相关文章索引3271
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Beilei Lei,Chaojian Wang,Kamie Snow et al. Beilei Lei et al.
Acute lung injury (ALI) is a syndrome of acute inflammation, barrier disruption, and hypoxemic respiratory failure associated with high morbidity and mortality. Diverse conditions lead to ALI, including inhalation of toxic substances, aspir...
Gayoung Jang,Ha Rim Shin,Hyo-Sang Do et al. Gayoung Jang et al.
Lesch-Nyhan syndrome (LNS) is inherited as an X-linked recessive genetic disorder caused by mutations in hypoxanthine-guanine phosphoribosyl transferase 1 (HPRT1). Patients with LNS show various clinical phenotypes, including hyperuricemia,...
Li Jinteng,Xu Peitao,Yu Wenhui et al. Li Jinteng et al.
During the aging process, the reduced osteogenic differentiation of bone marrow mesenchymal stem cells (BM-MSCs) results in decreased bone formation, which contributes to senile osteoporosis. Previous studies have confirmed that interrupted...
Huihui Fan,Jinze Li,Astrid M Manuel et al. Huihui Fan et al.
Prostate cancer is morphologically and molecularly heterogeneous, which poses obstacles for early diagnosis and treatment. Advancements in understanding the heterogeneity of prostate cancer will help navigate through these challenges and ul...
Melita Kaltak,Petra de Bruijn,Davide Piccolo et al. Melita Kaltak et al.
Stargardt disease type 1 (STGD1) is the most common hereditary form of maculopathy and remains untreatable. STGD1 is caused by biallelic variants in the ABCA4 gene, which encodes the ATP-binding cassette (type 4) protein (ABCA4) that clears...
Jing Su,Kaiqin She,Li Song et al. Jing Su et al.
Retinitis pigmentosa (RP) is a group of retinal diseases that cause the progressive death of retinal photoreceptor cells and eventually blindness. Mutations in the β-domain of the phosphodiesterase 6 (Pde6b) gene are the most identified ca...
Farkhad Maksudov,Evgenii Kliuchnikov,Daniel Pierson et al. Farkhad Maksudov et al.
Elucidating the structure-function relationships for therapeutic RNA mimicking phosphorodiamidate morpholino oligonucleotides (PMOs) is challenging due to the lack of information about their structures. While PMOs have been approved by the ...
Guiyang Zhang,Qiang Tang,Pengmian Feng et al. Guiyang Zhang et al.
The global pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has generated tremendous concern and poses a serious threat to international public health. Phosphorylation is a common post-translational modific...