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期刊名:Journal of neurogenetics

缩写:J NEUROGENET

ISSN:0167-7063

e-ISSN:1563-5260

IF/分区:1.8/Q4

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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
Saikat Dey,Monojit Debnath,Ramchandra Yelamanchi et al. Saikat Dey et al.
Genes play an important role in the risk of Progressive Supranuclear Palsy (PSP). Some of the major risk genes identified for PSP include MAPT, STX6, MOBP, and EIF2AK3 in several ethnic groups. However, the interactions among these genes ha...
Xin Zhao,Xinyu Li,Hua Bai et al. Xin Zhao et al.
Forgetting behavior is a common phenomenon that has been widely studied in various model organisms, including Caenorhabditis elegans (C. elegans), Drosophila, and mammals such as mice and humans. Understanding the mechanisms underlying forg...
Aurelia Vania,Dewa Putu Gde Purwa Samatra,I Made Oka Adnyana et al. Aurelia Vania et al.
Painful diabetic neuropathy (PDN) is a common complication in patients with type 2 diabetes mellitus (T2DM) with disruption of vitamin D (VD) activity as one of the risk factors. Active VD exerts its biological functions through the vitamin...
Wei-Sheng Lin Wei-Sheng Lin
Leigh syndrome spectrum is the most common form of childhood-onset mitochondrial encephalopathy and is characterized by progressive neurodegeneration. Treatment options for this condition remain limited to date. Nonetheless, two lines of re...
Deepanshu N D Singh,Matthias Soller Deepanshu N D Singh
Males transfer many components in seminal fluid along with sperm during mating. While sex peptide is well established as a key regulator of female reproductive behaviour and success, the roles of other seminal fluid components remain less u...
Marek B Körner,Akhil Velluva,Linnaeus Bundalian et al. Marek B Körner et al.
Pathogenic variants in WDFY3, a gene encoding for an autophagy adaptor termed ALFY, are linked to neurodevelopmental delay and altered brain size in human probands. While the role of WDFY3 loss-of-function is extensively studied in neurons,...