| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Qin Kang, Shishi Jiang, Jun Min, Fan Hu, Renshi X. Parvalbumin interneurons dysfunction is potentially associated with FαMNs decrease and NRG1-ErbB4 signaling inhibition in spinal cord in amyotrophic lateral sclerosis. Aging. vol 15. 2023-12-29. PMID:38157256. |
parvalbumin interneurons dysfunction is potentially associated with fαmns decrease and nrg1-erbb4 signaling inhibition in spinal cord in amyotrophic lateral sclerosis. |
2023-12-29 |
2024-01-05 |
Not clear |
| Saadat Ullah Khan, Muhammad Majid, Marius George Linguraru, Syed Muhammad Anwa. Upper Limb Movement Execution Classification using Electroencephalography for Brain Computer Interface. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference. vol 2023. 2023-12-12. PMID:38082727. |
decoding eeg-based upper limb movements can be of great help to people with spinal cord injury (sci) or other neuro-muscular diseases such as amyotrophic lateral sclerosis (als), primary lateral sclerosis, and periodic paralysis. |
2023-12-12 |
2023-12-17 |
human |
| Haiyang Ma, Jia Huo, Cheng Xin, Jing Yang, Qi Liu, Hui Dong, Rui Li, Yaling Li. RABGGTB plays a critical role in ALS pathogenesis. Brain research bulletin. 2023-12-02. PMID:38042502. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease with unknown causes, which mainly affects motor neurons in the anterior horn of the spinal cord, brain stem, and cerebral cortex, also known as motor neuron disease. |
2023-12-02 |
2023-12-10 |
Not clear |
| Alexander Fröhlich, Abigail L Pfaff, Vivien J Bubb, John P Quinn, Sulev Kok. Transcriptomic profiling of cerebrospinal fluid identifies ALS pathway enrichment and RNA biomarkers in MND individuals. Experimental biology and medicine (Maywood, N.J.). 2023-11-25. PMID:38001563. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disorder and the most common form of motor neurone disease (mnd) which is characterized by the damage and death of motor neurons in the brain and spinal cord of affected individuals. |
2023-11-25 |
2023-11-28 |
Not clear |
| Elisa Duranti, Chiara Vill. Muscle Involvement in Amyotrophic Lateral Sclerosis: Understanding the Pathogenesis and Advancing Therapeutics. Biomolecules. vol 13. issue 11. 2023-11-25. PMID:38002264. |
amyotrophic lateral sclerosis (als) is a fatal condition characterized by the selective loss of motor neurons in the motor cortex, brainstem, and spinal cord. |
2023-11-25 |
2023-11-28 |
Not clear |
| Chung-Min Wu, Yeou-Jiunn Chen, Shih-Chung Chen, Sheng-Feng Zhen. Creating an AI-Enhanced Morse Code Translation System Based on Images for People with Severe Disabilities. Bioengineering (Basel, Switzerland). vol 10. issue 11. 2023-11-25. PMID:38002405. |
(1) background: patients with severe physical impairments (spinal cord injury, cerebral palsy, amyotrophic lateral sclerosis) often have limited mobility due to physical limitations, and may even be bedridden all day long, losing the ability to take care of themselves. |
2023-11-25 |
2023-11-28 |
Not clear |
| Shaherin Basith, Balachandran Manavalan, Gwang Le. Unveiling local and global conformational changes and allosteric communications in SOD1 systems using molecular dynamics simulation and network analyses. Computers in biology and medicine. vol 168. 2023-11-21. PMID:37988788. |
amyotrophic lateral sclerosis (als) is a serious neurodegenerative disorder affecting nerve cells in the brain and spinal cord that is caused by mutations in the superoxide dismutase 1 (sod1) enzyme. |
2023-11-21 |
2023-11-29 |
Not clear |
| Aniket Saini, Pooja A Chawl. Breaking barriers with tofersen: Enhancing therapeutic opportunities in amyotrophic lateral sclerosis. European journal of neurology. 2023-11-17. PMID:37975798. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease that primarily affects adults, characterized by muscle weakness resulting from the specific death of motor neurons in the spinal cord and brain. |
2023-11-17 |
2023-11-20 |
Not clear |
| Dipnarine Maharaj, Kawaljit Kaur, Adrian Saltese, Jacqueline Gouve. Personalized Precision Immunotherapy for Amyotrophic Lateral Sclerosis (ALS). Critical reviews in immunology. vol 43. issue 2. 2023-11-08. PMID:37938192. |
neurological syndrome amyotrophic lateral sclerosis (als) affects motor neurons and is characterized by progressive motor neuron loss in the brain and spinal cord. |
2023-11-08 |
2023-11-20 |
Not clear |
| Julie J Ahn, Robert H Miller, Yusra Isla. Isolation of Pure Astrocytes and Microglia from the Adult Mouse Spinal Cord For In Vitro Assays and Transcriptomic Studies. Journal of visualized experiments : JoVE. issue 200. 2023-11-06. PMID:37930016. |
furthermore, focusing on spinal cord-specific isolation, excluding brain involvement, enables research into spinal cord pathologies, including experimental autoimmune encephalomyelitis, spinal cord injury, and amyotrophic lateral sclerosis. |
2023-11-06 |
2023-11-08 |
mouse |
| Anca Moțățăianu, Georgiana Șerban, Sebastian Andon. The Role of Short-Chain Fatty Acids in Microbiota-Gut-Brain Cross-Talk with a Focus on Amyotrophic Lateral Sclerosis: A Systematic Review. International journal of molecular sciences. vol 24. issue 20. 2023-10-30. PMID:37894774. |
amyotrophic lateral sclerosis is a devastating neurodegenerative disease characterized by the gradual loss of motor neurons in the brain and spinal cord, leading to progressive motor function decline. |
2023-10-30 |
2023-11-08 |
Not clear |
| Jun-Yang Liu, Yuan-Rong Lu, Jie Guo, Hua Li, Yuan Wang, Ying-Qian Zhao, Jie Li, Qiang Wan. Effect of electroacupuncture intervention on the spinal cord PPIA/NF-κB signaling pathway in mice with amyotrophic lateral sclerosis. Zhen ci yan jiu = Acupuncture research. vol 48. issue 10. 2023-10-25. PMID:37879951. |
effect of electroacupuncture intervention on the spinal cord ppia/nf-κb signaling pathway in mice with amyotrophic lateral sclerosis. |
2023-10-25 |
2023-11-08 |
mouse |
| Lijun Zhou, Wenzhi Chen, Shishi Jiang, Renshi X. In Vitro Models of Amyotrophic Lateral Sclerosis. Cellular and molecular neurobiology. 2023-10-23. PMID:37870685. |
amyotrophic lateral sclerosis (als) is one of the commonest neurodegenerative diseases of adult-onset, which is characterized by the progressive death of motor neurons in the cerebral cortex, brain stem and spinal cord. |
2023-10-23 |
2023-11-08 |
Not clear |
| Matthew W Holt, Eric C Robinson, Nathan A Shlobin, Jacob T Hanson, Ismail Bozkur. Intracortical brain-computer interfaces for improved motor function: a systematic review. Reviews in the neurosciences. 2023-10-17. PMID:37845811. |
the systems treated patients with various conditions: amyotrophic lateral sclerosis, stroke, spinocerebellar degeneration without cerebellar involvement, and spinal cord injury. |
2023-10-17 |
2023-11-08 |
human |
| Xinxin Wang, Yushu Hu, Renshi X. The pathogenic mechanism of TAR DNA-binding protein 43 (TDP-43) in amyotrophic lateral sclerosis. Neural regeneration research. vol 19. issue 4. 2023-10-16. PMID:37843214. |
the onset of amyotrophic lateral sclerosis is usually characterized by focal death of both upper and/or lower motor neurons occurring in the motor cortex, basal ganglia, brainstem, and spinal cord, and commonly involves the muscles of the upper and/or lower extremities, and the muscles of the bulbar and/or respiratory regions. |
2023-10-16 |
2023-11-08 |
Not clear |
| Soo Yeon Lee, Hye-Yeon Cho, Jung-Pyo Oh, Jiae Park, Sang-Hun Bae, Haesun Park, Eun Jung Kim, Ji-Hyun Le. Therapeutic Effects of Combination of Nebivolol and Donepezil: Targeting Multifactorial Mechanisms in ALS. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics. 2023-10-02. PMID:37782409. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disorder characterized by progressive loss of motor neurons in the spinal cord. |
2023-10-02 |
2023-10-07 |
Not clear |
| Di Chen, Hongyun Huang, Hooshang Saberi, Hari Shanker Sharm. Positive and negative cell therapy in randomized control trials for central nervous system diseases. International review of neurobiology. vol 171. 2023-10-02. PMID:37783557. |
in this review, we summarized randomized clinical trials of cell therapies for central nervous diseases, such as stroke, spinal cord injury, cerebral palsy (cp), parkinson's disease (pd), multiple sclerosis (ms), brain trauma, amyotrophic lateral sclerosis (als), etc. |
2023-10-02 |
2023-10-07 |
Not clear |
| Wanglin Dong, Qianwen Peng, Zhuoxin Liu, Zhenxing Xie, Xiajun Guo, Yuanyuan Li, Chaoran Che. Estrogen plays an important role by influencing the NLRP3 inflammasome. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. vol 167. 2023-09-22. PMID:37738797. |
estrogen can ameliorate some diseases (e. g, sepsis, mood disturbances, cerebral ischemia, some hepatopathy, parkinson's disease, amyotrophic lateral sclerosis, inflammatory bowel disease, spinal cord injury, multiple sclerosis, myocardial ischemia/reperfusion injury, osteoarthritis, and renal fibrosis) by inhibiting the nlrp3 inflammasome. |
2023-09-22 |
2023-10-07 |
Not clear |
| Serenella Anzilotti, Valeria Valente, Paola Brancaccio, Cristina Franco, Antonella Casamassa, Giovanna Lombardi, Alessandra Palazzi, Andrea Conte, Simona Paladino, Lorella Maria Teresa Canzoniero, Lucio Annunziato, Giovanna Maria Pierantoni, Giuseppe Pignatar. Chronic exposure to l-BMAA cyanotoxin induces cytoplasmic TDP-43 accumulation and glial activation, reproducing an amyotrophic lateral sclerosis-like phenotype in mice. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. vol 167. 2023-09-20. PMID:37729728. |
amyotrophic lateral sclerosis (als) is a progressive and often fatal neurodegenerative disease characterized by the loss of motor neurons (mns) in spinal cord, motor cortex and brainstem. |
2023-09-20 |
2023-10-07 |
mouse |
| Jin Gao, Mingchen Jiang, Danilo Erricolo, Richard L Magin, Gerardo Morfini, Thomas Royston, Andrew C Larson, Weiguo L. Identifying potential imaging markers for diffusion property changes in a mouse model of amyotrophic lateral sclerosis: Application of the continuous time random walk model to ultrahigh b-value diffusion-weighted MR images of spinal cord tissue. NMR in biomedicine. 2023-09-18. PMID:37721118. |
identifying potential imaging markers for diffusion property changes in a mouse model of amyotrophic lateral sclerosis: application of the continuous time random walk model to ultrahigh b-value diffusion-weighted mr images of spinal cord tissue. |
2023-09-18 |
2023-10-07 |
mouse |