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期刊名:Neuromolecular medicine

缩写:NEUROMOL MED

ISSN:1535-1084

e-ISSN:1559-1174

IF/分区:3.9/Q2

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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
María Fernanda Serna-Rodríguez,Oscar Cienfuegos-Jiménez,Ricardo Martín Cerda-Flores et al. María Fernanda Serna-Rodríguez et al.
Suicide is a global public health issue, with a particularly high incidence in individuals suffering from Major Depressive Disorder (MDD). The role of cholesterol in suicide risk remains controversial, prompting investigations into genetic ...
Oak Z Chi,Xia Liu,Harvey Fortus et al. Oak Z Chi et al.
The manifestations of tuberous sclerosis complex (TSC) in humans include epilepsy, autism spectrum disorders (ASD) and intellectual disability. Previous studies suggested the linkage of TSC to altered cerebral blood flow and metabolic dysfu...
Baojian Guo,Chengyou Zheng,Jie Cao et al. Baojian Guo et al.
Aggregation of α-synuclein (α-syn) and α-syn cytotoxicity are hallmarks of sporadic and familial Parkinson's disease (PD). Nuclear factor (erythroid-derived 2)-like 2 (Nrf2)-dependent enhancement of the expression of the 20S proteasome c...
Ankit Patel,Ashutosh Dharap Ankit Patel
Noncoding DNA undergoes widespread context-dependent transcription to produce noncoding RNAs. In recent decades, tremendous advances in genomics and transcriptomics have revealed important regulatory roles for noncoding DNA elements and the...
V V Guzenko,S S Bachurin,V A Dzreyan et al. V V Guzenko et al.
This study focuses on understanding the role of c-Myc, a cancer-associated transcription factor, in the penumbra following ischemic stroke. While its involvement in cell death and survival is recognized, its post-translational modifications...
Limin Ma,Fengyu Wang,Shuai Chen et al. Limin Ma et al.
Familial Alzheimer's disease (AD) is a rare disease caused by autosomal-dominant mutations. APP (encoding amyloid precursor protein), PSEN1 (encoding presenilin 1), and PSEN2 (encoding presenilin 2) are the most common genes cause dominant ...
Antonio Musarò,Gabriella Dobrowolny,Chiara Cambieri et al. Antonio Musarò et al.
Amyotrophic lateral sclerosis (ALS) is a rare neuromuscular disease with a wide disease progression. Despite several efforts to develop efficient biomarkers, many concerns about the available ones still need to be addressed. MicroRNA (miR) ...
Esen Yilmaz,Gozde Acar,Ummugulsum Onal et al. Esen Yilmaz et al.
Background: Ischemic stroke is the leading cause of mortality and disability worldwide with more than half of survivors living with serious neurological sequelae; thus, it has recently attracted a lot of attention in the ...
Mydhili Radhakrishnan,Vincy Vijay,B Supraja Acharya et al. Mydhili Radhakrishnan et al.
Cerebral ischemic stroke is one of the foremost global causes of death and disability. Due to inadequate knowledge in its sequential disease mechanisms, therapeutic efforts to mitigate acute ischemia-induced brain injury are limited. Recent...
Roberto Federico Villa,Federica Ferrari,Antonella Gorini Roberto Federico Villa
In this study the subcellular modifications undergone by cerebral cortex mitochondrial metabolism in chronic hypertension during aging were evaluated. The catalytic properties of regulatory energy-linked enzymes of Tricarboxylic Acid Cycle ...