Frontiers in molecular neuroscience

· 7 papers in corpus
lab-animal 2024
doi:10.3389/fnmol.2024.1160435 ·PMID:38783903

The function of peripheral nociceptors, the neurons that relay pain signals to the brain, are frequently tuned by local and systemic modulator substances. In this context, neurohormonal effects are emerging as an important modulatory mechan…

lab-animal 2024
doi:10.3389/fnmol.2024.1335404 ·PMID:38361743

INTRODUCTION: Menstrual blood-derived stem cells (MenSCs) are vital in treating many degenerative and traumatic disorders. However, the underlying molecular mechanisms remain obscure in MenSCs-treating spinal cord injury (SCI) rats. METHOD…

review 2023
doi:10.3389/fnmol.2023.1237429 ·PMID:38025263

Since the middle of the 20th century, synthetic sex hormones (estrogens and progestins) have been administered to millions of pregnant or not women worldwide, mainly to avoid miscarriage or for comfort, although their mode of action and the…

review 2022
doi:10.3389/fnmol.2022.931704 ·PMID:35782387

Central nervous system (CNS) disorders, such as ischemic stroke, Alzheimer's disease, Parkinson's disease, spinal cord injury, glioma, and epilepsy, involve oxidative stress and neuronal apoptosis, often leading to long-term disability or d…

other 2022
doi:10.3389/fnmol.2022.1022463 ·PMID:36683850

BACKGROUND: Visceral pain is a complex and heterogeneous disorder that is considered more prominent compared to somatic pain, due to its multiple and complex causes and accompanying emotional and mood disorders. Research has become increasi…

lab-animal 2018
doi:10.3389/fnmol.2018.00259 ·PMID:30154697

To obtain a thorough understanding of chronic pain, large-scale molecular mapping of the pain axis at the protein level is necessary, but has not yet been achieved. We applied quantitative proteome profiling to build a comprehensive protein…

review 2017
doi:10.3389/fnmol.2017.00290 ·PMID:28955201

Fragile X syndrome (FXS), is caused by a loss-of-function mutation in the FMR1 gene located on the X-chromosome, which leads to the most common cause of inherited intellectual disability in males and the leading single-gene defect associate…