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期刊名:Plos genetics

缩写:PLOS GENET

ISSN:1553-7404

e-ISSN:1553-7404

IF/分区:3.7/Q2

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共收录本刊相关文章索引10991
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
Allison T Mezzell,Yu Zhang,Alexandra M Perez et al. Allison T Mezzell et al.
Oculopharyngeal muscular dystrophy (OPMD) is a late-onset disease caused by modest alanine expansion at the amino terminus of the nuclear polyadenosine RNA binding protein PABPN1. PABPN1 is expressed ubiquitously and is involved in multiple...
Chi Zhang,Geyu Zhou,Tianqi Chen et al. Chi Zhang et al.
Recent years have witnessed a surge in the development of innovative polygenic score (PGS) methods, driving their extensive application in disease prevention, monitoring, and treatment. However, the accuracy of genetic risk prediction remai...
Liling Lin,Yankai Li,Fengtao Ji et al. Liling Lin et al.
Background: Fibromyalgia, insomnia, depression, and anxiety share common clinical comorbidities, but their underlying genetic architecture and mechanism remain unclear. ...
Bhagaban Mallik,Shikha Kushwaha,Anjali Bisht et al. Bhagaban Mallik et al.
Calcium release from intracellular stores influences synaptic response timing and magnitude. Despite the critical role of inositol trisphosphate (IP3)- and ryanodine receptor (RyR)-dependent calcium release in regulating synaptic strength, ...
Sudhir Kumar,Xueping Fan,Harshita Pattam et al. Sudhir Kumar et al.
Mowat-Wilson Syndrome (MWS) is an autosomal dominant genetic disorder caused by heterozygous mutations or deletions in the Zinc finger E-box-binding homeobox 2 (ZEB2) gene. Congenital anomalies of the kidney and urinary tract (CAKUT), inclu...
Yang Fu,Xu Bai,Lei Chun et al. Yang Fu et al.
Copper is an essential micronutrient for all living organisms. Mutations in the copper-importing transporter CTR1/CHCA-1 are associated with a severe copper deficiency disorder in humans, for which no effective cures are currently available...
Vikas Shukla,Elin Axelsson,Tetsuya Hisanaga et al. Vikas Shukla et al.
The complexity of varied modifications of chromatin composition is integrated in archetypal combinations called chromatin states that predict the local potential for transcription. The degree of conservation of chromatin states has not been...
Alice Gadau,Sasha Mills,Xin Yu Zhu Jiang et al. Alice Gadau et al.
Organisms evolve behavioral and morphological traits to adapt to their ecological niches, yet the genetic basis of adaptation remains largely unknown. Drosophila suzukii has evolved a distinctive oviposition preference for ripe fruit, unlik...
Can Tian,Pei-Yao Feng,Lin Wang et al. Can Tian et al.
Matrix metalloproteinases (MMPs) play crucial roles in both physiological and pathological conditions by degrading the extracellular matrix; however, the roles and regulatory mechanisms of MMPs in brain development remain insufficiently und...
Shruti Thapliyal,Amruta Vasudevan,Yongming Dong et al. Shruti Thapliyal et al.
[This corrects the article DOI: 10.1371/journal.pgen.1007263.]. Copyright: © 2026 Thapliyal et al. This is an open access article distributed under the ...