| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| J P J M de Munter, J Mey, T Strekalova, B W Kramer, E Ch Wolter. Why do anti-inflammatory signals of bone marrow-derived stromal cells improve neurodegenerative conditions where anti-inflammatory drugs fail? Journal of neural transmission (Vienna, Austria : 1996). vol 127. issue 5. 2021-06-14. PMID:32253536. |
the benefit of bm-scs was demonstrated in rats with an acute (traumatic spinal cord injury, tsci) and in mice with a chronic [amyotrophic lateral sclerosis (als)-like fus 1-358 or sod1-g93-a mutation] neurodegenerative process. |
2021-06-14 |
2023-08-13 |
mouse |
| Svitlana Garbuzova-Davis, Robert Shell, Hilmi Mustafa, Surafuale Hailu, Alison E Willing, Paul R Sanberg, Cesario V Borlonga. Advancing Stem Cell Therapy for Repair of Damaged Lung Microvasculature in Amyotrophic Lateral Sclerosis. Cell transplantation. vol 29. 2021-06-08. PMID:32207340. |
amyotrophic lateral sclerosis (als) is a fatal disease of motor neuron degeneration in the brain and spinal cord. |
2021-06-08 |
2023-08-13 |
mouse |
| Xia-Wei Liu, Ying Yan, Yi-Fan Hei, Chen-Jun Zhu, Qing Tian, Wen-Jun Su. [Effect of electroacupuncture on expression of heat shock protein 70 in mice with amyotrophic lateral sclerosis]. Zhen ci yan jiu = Acupuncture research. vol 46. issue 5. 2021-06-07. PMID:34085462. |
to observe the effects of electroacupuncture (ea) on the body weight, disease progression and the expression of heat shock protein 70 (hsp70) in lumbar spinal cord of amyotrophic lateral sclerosis (als) mice, so as to explore the mechanism of ea on treating als. |
2021-06-07 |
2023-08-13 |
mouse |
| J M Gregory, E Elliott, K McDade, T Bak, S Pal, S Chandran, S Abrahams, C Smit. Neuronal clusterin expression is associated with cognitive protection in amyotrophic lateral sclerosis. Neuropathology and applied neurobiology. vol 46. issue 3. 2021-06-04. PMID:31386770. |
clusterin has been shown to be upregulated in the spinal cord of patients with amyotrophic lateral sclerosis (als) and has been shown to protect against tdp-43 protein misfolding in animal and cell models. |
2021-06-04 |
2023-08-13 |
Not clear |
| Fabiola De Marchi, Claudia Carrarini, Antonio De Martino, Luca Diamanti, Antonio Fasano, Antonino Lupica, Mirella Russo, Simone Salemme, Edoardo Gioele Spinelli, Alessandro Bombac. Cognitive dysfunction in amyotrophic lateral sclerosis: can we predict it? Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 42. issue 6. 2021-05-31. PMID:33772353. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disorder characterized by the degeneration of both upper and lower motoneurons in the brain and spinal cord leading to motor and extra-motor symptoms. |
2021-05-31 |
2023-08-13 |
Not clear |
| Regine Sitruk-Ware, Brooke Bonsack, Roberta Brinton, Michael Schumacher, Narender Kumar, Jea-Young Lee, Vanessa Castelli, Sydney Corey, Alexandreya Coats, Nadia Sadanandan, Bella Gonzales-Portillo, Matt Heyck, Alex Shear, Cozene Blaise, Henry Zhang, Michael Sheyner, Julián García-Sánchez, Lisset Navarro, Martine El-Etr, Alejandro F De Nicola, Cesar V Borlonga. Progress in progestin-based therapies for neurological disorders. Neuroscience and biobehavioral reviews. vol 122. 2021-05-27. PMID:33359391. |
that cns disorders, including multiple sclerosis (ms), amyotrophic lateral sclerosis (als), spinal cord injury (sci), and stroke, develop via demyelinating, cell death, and/or inflammatory pathological pathways advances nestorone as an auspicious candidate for these disorders. |
2021-05-27 |
2023-08-13 |
Not clear |
| Agnieszka Kulczyńska-Przybik, Piotr Mroczko, Maciej Dulewicz, Barbara Mroczk. The Implication of Reticulons (RTNs) in Neurodegenerative Diseases: From Molecular Mechanisms to Potential Diagnostic and Therapeutic Approaches. International journal of molecular sciences. vol 22. issue 9. 2021-05-26. PMID:33924890. |
the crucial role of rtns in the development of several neurodegenerative diseases, including alzheimer's disease (ad), multiple sclerosis (ms), amyotrophic lateral sclerosis (als), or other neurological conditions such as brain injury or spinal cord injury, has attracted scientific interest. |
2021-05-26 |
2023-08-13 |
Not clear |
| Yanran Li, Bo Sun, Zhanjun Wang, Zhengqing He, Fei Yang, Hongfen Wang, Fang Cui, Zhaohui Chen, Li Ling, Chaodong Wang, Xusheng Huan. Mutation Screening of the Frontiers in neuroscience. vol 15. 2021-05-26. PMID:34025336. |
mutation screening of the amyotrophic lateral sclerosis (als) is a fatal progressive neurodegenerative disease involving the upper and lower motor neurons of the spinal cord, brainstem, and cerebral cortex. |
2021-05-26 |
2023-08-13 |
Not clear |
| Eiichiro Nagata, Natsuko Fujii, Saori Kohara, Chisa Okada, Tadayuki Satoh, Susumu Takekoshi, Masaki Takao, Ban Mihara, Shunya Takizaw. Inositol hexakisphosphate kinase 2 promotes cell death of anterior horn cells in the spinal cord of patients with amyotrophic lateral sclerosis. Molecular biology reports. vol 47. issue 9. 2021-05-25. PMID:32929655. |
inositol hexakisphosphate kinase 2 promotes cell death of anterior horn cells in the spinal cord of patients with amyotrophic lateral sclerosis. |
2021-05-25 |
2023-08-13 |
Not clear |
| Carmen Hummel, Omid Leylamian, Anna Pösch, Joachim Weis, Eleonora Aronica, Cordian Beyer, Sonja Johan. Expression and Cell Type-specific Localization of Inflammasome Sensors in the Spinal Cord of SOD1 Neuroscience. vol 463. 2021-05-19. PMID:33781799. |
expression and cell type-specific localization of inflammasome sensors in the spinal cord of sod1 inflammasomes are key components of the innate immune system and activation of these multiprotein platforms is a crucial event in the etiopathology of amyotrophic lateral sclerosis (als). |
2021-05-19 |
2023-08-13 |
Not clear |
| Omar Deeb, Maisa Nabuls. Exploring Multiple Sclerosis (MS) and Amyotrophic Lateral Scler osis (ALS) as Neurodegenerative Diseases and their Treatments: A Review Study. Current topics in medicinal chemistry. vol 20. issue 26. 2021-05-17. PMID:32972341. |
amyotrophic lateral sclerosis (als) is another neurodegenerative disease that is characterized by the degeneration of motor neurons in the brain and spinal cord. |
2021-05-17 |
2023-08-13 |
Not clear |
| Chong Liu, Dongxiao Li, Cui Lv, Zhisong Gao, Yinkuang Qi, Hongran Wu, Yunyun Tian, Yansu Gu. Activation of the Notch Signaling Pathway and Cellular Localization of Notch Signaling Molecules in the Spinal Cord of SOD1-G93A ALS Model Mice. Neuroscience. vol 432. 2021-05-14. PMID:32114100. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disorder characterized by motor neuron loss and gliosis in the spinal cord, brain stem and cortex. |
2021-05-14 |
2023-08-13 |
mouse |
| Alina Salamatina, Jerry H Yang, Susan Brenner-Morton, Jay B Bikoff, Linjing Fang, Christopher R Kintner, Thomas M Jessell, Lora B Sweene. Differential Loss of Spinal Interneurons in a Mouse Model of ALS. Neuroscience. vol 450. 2021-05-14. PMID:32858144. |
amyotrophic lateral sclerosis (als) leads to a loss of specific motor neuron populations in the spinal cord and cortex. |
2021-05-14 |
2023-08-13 |
mouse |
| Lin Wang, Lijuan Zhan. MicroRNAs in amyotrophic lateral sclerosis: from pathogenetic involvement to diagnostic biomarker and therapeutic agent development. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 41. issue 12. 2021-05-14. PMID:33006054. |
amyotrophic lateral sclerosis (als) is a fatal neurodegenerative disease with an unclear etiology and is characterized by the selective invasion of motor neurons in the brain and spinal cord. |
2021-05-14 |
2023-08-13 |
Not clear |
| Julia Post, Vanessa Kogel, Anja Schaffrath, Philipp Lohmann, N Jon Shah, Karl-Josef Langen, Dieter Willbold, Antje Willuweit, Janine Kutzsch. A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model. Molecules (Basel, Switzerland). vol 26. issue 6. 2021-05-12. PMID:33805709. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease characterised by selective neuronal death in the brain stem and spinal cord. |
2021-05-12 |
2023-08-13 |
mouse |
| Luigi Montibeller, Li Yi Tan, Joo Kyung Kim, Praveen Paul, Jacqueline de Belleroch. Tissue-selective regulation of protein homeostasis and unfolded protein response signalling in sporadic ALS. Journal of cellular and molecular medicine. vol 24. issue 11. 2021-04-28. PMID:32324341. |
amyotrophic lateral sclerosis (als) is a disorder that affects motor neurons in motor cortex and spinal cord, and the degeneration of both neuronal populations is a critical feature of the disease. |
2021-04-28 |
2023-08-13 |
human |
| Edmund Charles Jenkins, Gabriella Casalena, Maria Gomez, Dazhi Zhao, Timothy C Kenny, Nagma Shah, Giovanni Manfredi, Doris Germai. Raloxifene is a Female-specific Proteostasis Therapeutic in the Spinal Cord. Endocrinology. vol 162. issue 2. 2021-04-28. PMID:33269387. |
in the sod1-g93a mouse model of amyotrophic lateral sclerosis, we found that even a low dose of raloxifene causes a significant decrease in mutant sod1 aggregates in the spinal cord, accompanied by a delay in the decline of muscle strength in females, but not in males. |
2021-04-28 |
2023-08-13 |
mouse |
| Kyriakos Dalamagkas, Magdalini Tsintou, Yogesh Rathi, Lauren J O'Donnell, Ofer Pasternak, Xue Gong, Anne Zhu, Peter Savadjiev, George M Papadimitriou, Marek Kubicki, Edward H Yeterian, Nikos Makri. Individual variations of the human corticospinal tract and its hand-related motor fibers using diffusion MRI tractography. Brain imaging and behavior. vol 14. issue 3. 2021-04-27. PMID:30617788. |
its clinical significance can be demonstrated in many notable traumatic conditions and diseases such as stroke, spinal cord injury (sci) or amyotrophic lateral sclerosis (als). |
2021-04-27 |
2023-08-13 |
human |
| Patcharin Phokasem, Salinee Jantrapirom, Jirarat Karinchai, Hideki Yoshida, Masamitsu Yamaguchi, Panuwan Chantawannaku. Honeybee products and edible insect powders improve locomotive and learning abilities of Ubiquilin-knockdown Drosophila. BMC complementary medicine and therapies. vol 20. issue 1. 2021-04-21. PMID:32867756. |
mutations in the human ubiquilin 2 gene are associated with neurodegenerative diseases such as amyotrophic lateral sclerosis (als) with or without frontotemporal dementia (ftd), the fatal neurodegenerative disease that progressively affected neuronal cells in both brain and spinal cord. |
2021-04-21 |
2023-08-13 |
human |
| Matt Keon, Benjamin Musrie, Marcel Dinger, Samuel E Brennan, Jerran Santos, Nitin K Saksen. Destination Amyotrophic Lateral Sclerosis. Frontiers in neurology. vol 12. 2021-04-16. PMID:33854469. |
amyotrophic lateral sclerosis (als) is a prototypical neurodegenerative disease characterized by progressive degeneration of motor neurons both in the brain and spinal cord. |
2021-04-16 |
2023-08-13 |
Not clear |