| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Anna Nigri, Eleonora Dalla Bella, Stefania Ferraro, Jean Paul Medina Carrion, Greta Demichelis, Enrica Bersano, Monica Consonni, Antje Bischof, Mario Stanziano, Sara Palermo, Giuseppe Lauria, Maria Grazia Bruzzone, Nico Papinutt. Cervical spinal cord atrophy in amyotrophic lateral sclerosis across disease stages. Annals of clinical and translational neurology. 2023-01-04. PMID:36599092. |
cervical spinal cord atrophy in amyotrophic lateral sclerosis across disease stages. |
2023-01-04 |
2023-08-14 |
Not clear |
| Anna Nigri, Eleonora Dalla Bella, Stefania Ferraro, Jean Paul Medina Carrion, Greta Demichelis, Enrica Bersano, Monica Consonni, Antje Bischof, Mario Stanziano, Sara Palermo, Giuseppe Lauria, Maria Grazia Bruzzone, Nico Papinutt. Cervical spinal cord atrophy in amyotrophic lateral sclerosis across disease stages. Annals of clinical and translational neurology. 2023-01-04. PMID:36599092. |
spinal cord degeneration is a hallmark of amyotrophic lateral sclerosis. |
2023-01-04 |
2023-08-14 |
Not clear |
| Anna Nigri, Eleonora Dalla Bella, Stefania Ferraro, Jean Paul Medina Carrion, Greta Demichelis, Enrica Bersano, Monica Consonni, Antje Bischof, Mario Stanziano, Sara Palermo, Giuseppe Lauria, Maria Grazia Bruzzone, Nico Papinutt. Cervical spinal cord atrophy in amyotrophic lateral sclerosis across disease stages. Annals of clinical and translational neurology. 2023-01-04. PMID:36599092. |
the assessment of gray matter and white matter cervical spinal cord atrophy across clinical stages defined using the king's staging system could advance the understanding of amyotrophic lateral sclerosis progression. |
2023-01-04 |
2023-08-14 |
Not clear |
| Prasamsa Pudasaini, Shashank Neupane, Bishal Dhakal, Abilasha Rana, Bishnu Deep Pathak, Sagun Dawad. Bulbar onset amyotrophic lateral sclerosis: A case report. Annals of medicine and surgery (2012). vol 84. 2022-12-30. PMID:36582871. |
amyotrophic lateral sclerosis is a rare progressive neurodegenerative disease that affects the brain and spinal cord nerve cells. |
2022-12-30 |
2023-08-14 |
Not clear |
| Long-Fang Tu, Tian-Ze Zhang, Yang-Fan Zhou, Qing-Qing Zhou, Hai-Biao Gong, Lei Liang, Lin-Na Hai, Nan-Xin You, Yang Su, Yong-Jun Chen, Xu-Kai Mo, Chang-Zheng Shi, Liang-Ping Luo, Wan-Yang Sun, Wen-Jun Duan, Hiroshi Kurihara, Yi-Fang Li, Rong-Rong H. GPX4 deficiency-dependent phospholipid peroxidation drives motor deficits of ALS. Journal of advanced research. vol 43. 2022-12-30. PMID:36585109. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease characterized by oxidative stress that triggers motor neurons loss in the brain and spinal cord. |
2022-12-30 |
2023-08-14 |
mouse |
| Fang Yang, Wen-Zhi Chen, Shi-Shi Jiang, Xiao-Hua Wang, Ren-Shi X. A candidate protective factor in amyotrophic lateral sclerosis: heterogenous nuclear ribonucleoprotein G. Neural regeneration research. vol 18. issue 7. 2022-12-26. PMID:36571358. |
a candidate protective factor in amyotrophic lateral sclerosis: heterogenous nuclear ribonucleoprotein g. heterogenous nuclear ribonucleoprotein g is down-regulated in the spinal cord of the tg(sod1*g93a)1gur (tg) amyotrophic lateral sclerosis mouse model. |
2022-12-26 |
2023-08-14 |
mouse |
| Fang Yang, Wen-Zhi Chen, Shi-Shi Jiang, Xiao-Hua Wang, Ren-Shi X. A candidate protective factor in amyotrophic lateral sclerosis: heterogenous nuclear ribonucleoprotein G. Neural regeneration research. vol 18. issue 7. 2022-12-26. PMID:36571358. |
we analyzed heterogenous nuclear ribonucleoprotein g distribution in spinal cord in the amyotrophic lateral sclerosis model at various time points and the expressions of apoptosis and proliferation-related proteins. |
2022-12-26 |
2023-08-14 |
mouse |
| Fang Yang, Wen-Zhi Chen, Shi-Shi Jiang, Xiao-Hua Wang, Ren-Shi X. A candidate protective factor in amyotrophic lateral sclerosis: heterogenous nuclear ribonucleoprotein G. Neural regeneration research. vol 18. issue 7. 2022-12-26. PMID:36571358. |
our study suggests that abnormal distribution and expression of heterogenous nuclear ribonucleoprotein g might play a protective effect in amyotrophic lateral sclerosis development via preventing neuronal death by reducing abnormal tar dna binding protein 43 generation in the spinal cord. |
2022-12-26 |
2023-08-14 |
mouse |
| Winanto Ng, Shi-Yan N. Remodeling of astrocyte secretome in amyotrophic lateral sclerosis: uncovering novel targets to combat astrocyte-mediated toxicity. Translational neurodegeneration. vol 11. issue 1. 2022-12-25. PMID:36567359. |
amyotrophic lateral sclerosis (als) is an adult-onset paralytic disease characterized by progressive degeneration of upper and lower motor neurons in the motor cortex, brainstem and spinal cord. |
2022-12-25 |
2023-08-14 |
Not clear |
| Yu Hashimoto, Ryo Yamasaki, Senri Ko, Eriko Matsuo, Yuko Kobayakawa, Katsuhisa Masaki, Dai Matsuse, Noriko Isob. Connexin 30 Deficiency Ameliorates Disease Progression at the Early Phase in a Mouse Model of Amyotrophic Lateral Sclerosis by Suppressing Glial Inflammation. International journal of molecular sciences. vol 23. issue 24. 2022-12-23. PMID:36555685. |
cx30 is upregulated on activated astroglia in central nervous system inflammatory lesions, including spinal cord lesions in mutant superoxide dismutase 1 (msod1) transgenic amyotrophic lateral sclerosis (als) model mice. |
2022-12-23 |
2023-08-14 |
mouse |
| Jennifer L Sippel, Jennifer E Daly, Linda Poggensee, Kim D Ristau, Adam C Eberhart, Katharine Tam, Charlesnika T Evans, Betsy Lancaster, I Manosha Wickremasinghe, Stephen P Burns, Barry Goldstein, Bridget M Smit. Modernization of a Large Spinal Cord Injuries and Disorders Registry: The Veterans Administration Experience. Archives of rehabilitation research and clinical translation. vol 4. issue 4. 2022-12-22. PMID:36545529. |
the vsr also comprises one of the only registries for individuals with non-traumatic sci/ds and holds potential to advance research and treatment for multiple sclerosis (ms), amyotrophic lateral sclerosis (als), and other motor neuron disorders with spinal cord involvement. |
2022-12-22 |
2023-08-14 |
Not clear |
| JingSi Jiang, Yan Wang, Min Den. New developments and opportunities in drugs being trialed for amyotrophic lateral sclerosis from 2020 to 2022. Frontiers in pharmacology. vol 13. 2022-12-15. PMID:36518658. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disorder that primarily affects motor neurons in the brain and spinal cord. |
2022-12-15 |
2023-08-14 |
Not clear |
| Jack Humphrey, Sanan Venkatesh, Rahat Hasan, Jake T Herb, Katia de Paiva Lopes, Fahri Küçükali, Marta Byrska-Bishop, Uday S Evani, Giuseppe Narzisi, Delphine Fagegaltier, Kristel Sleegers, Hemali Phatnani, David A Knowles, Pietro Fratta, Towfique Ra. Integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genes. Nature neuroscience. 2022-12-09. PMID:36482247. |
integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genes. |
2022-12-09 |
2023-08-14 |
Not clear |
| Jack Humphrey, Sanan Venkatesh, Rahat Hasan, Jake T Herb, Katia de Paiva Lopes, Fahri Küçükali, Marta Byrska-Bishop, Uday S Evani, Giuseppe Narzisi, Delphine Fagegaltier, Kristel Sleegers, Hemali Phatnani, David A Knowles, Pietro Fratta, Towfique Ra. Integrative transcriptomic analysis of the amyotrophic lateral sclerosis spinal cord implicates glial activation and suggests new risk genes. Nature neuroscience. 2022-12-09. PMID:36482247. |
amyotrophic lateral sclerosis (als) is a progressively fatal neurodegenerative disease affecting motor neurons in the brain and spinal cord. |
2022-12-09 |
2023-08-14 |
Not clear |
| Ryan A Milstead, Christopher D Link, Zuoshang Xu, Charles A Hoeffe. TDP-43 knockdown in mouse model of ALS leads to dsRNA deposition, gliosis, and neurodegeneration in the spinal cord. Cerebral cortex (New York, N.Y. : 1991). 2022-11-28. PMID:36443249. |
transactive response dna binding protein 43 kilodaltons (tdp-43) is a dna and rna binding protein associated with severe neurodegenerative diseases such as amyotrophic lateral sclerosis (als), primarily affecting motor neurons in the brain and spinal cord. |
2022-11-28 |
2023-08-14 |
mouse |
| Juan José Casañas, María Luz Montesino. Proteomic characterization of spinal cord synaptoneurosomes from Tg-SOD1/G93A mice supports a role for MNK1 and local translation in the early stages of amyotrophic lateral sclerosis. Molecular and cellular neurosciences. 2022-11-13. PMID:36372157. |
proteomic characterization of spinal cord synaptoneurosomes from tg-sod1/g93a mice supports a role for mnk1 and local translation in the early stages of amyotrophic lateral sclerosis. |
2022-11-13 |
2023-08-14 |
mouse |
| Juan José Casañas, María Luz Montesino. Proteomic characterization of spinal cord synaptoneurosomes from Tg-SOD1/G93A mice supports a role for MNK1 and local translation in the early stages of amyotrophic lateral sclerosis. Molecular and cellular neurosciences. 2022-11-13. PMID:36372157. |
to characterize synaptic failure in the spinal cord (sc) in the tg-sod1/g93a mouse model of amyotrophic lateral sclerosis (als), we applied a method we originally designed to isolate cortical and hippocampal sns to sc tissue. |
2022-11-13 |
2023-08-14 |
mouse |
| Shirong Li, Junyu Lin, Chunyu Li, Yongping Chen, Bei Cao, Tianmi Yang, Qianqian Wei, Bi Zhao, Xueping Chen, Huifang Shan. Clinical and genetic study of a Chinese family affected by both amyotrophic lateral sclerosis and autosomal dominant polycystic kidney disease. Frontiers in neurology. vol 13. 2022-11-07. PMID:36341123. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disorder characterized by loss of the upper and lower motor neurons from the motor cortex, brainstem, and spinal cord. |
2022-11-07 |
2023-08-14 |
Not clear |
| Giuseppe Schirò, Vincenzo Di Stefano, Salvatore Iacono, Antonino Lupica, Filippo Brighina, Roberto Monastero, Carmela Rita Balistrer. Advances on Cellular Clonotypic Immunity in Amyotrophic Lateral Sclerosis. Brain sciences. vol 12. issue 10. 2022-10-27. PMID:36291345. |
amyotrophic lateral sclerosis (als) is a fatal neuromuscular disease, characterized by the progressive degeneration of the upper and lower motor neurons in the cortex and spinal cord. |
2022-10-27 |
2023-08-14 |
human |
| Yoshitaka Tamaki, Makoto Urushitan. Molecular Dissection of TDP-43 as a Leading Cause of ALS/FTLD. International journal of molecular sciences. vol 23. issue 20. 2022-10-27. PMID:36293362. |
hyperphosphorylated and ubiquitinated tdp-43-positive neuronal cytoplasmic inclusions are identified in the brain and spinal cord in most cases of amyotrophic lateral sclerosis (als) and a substantial proportion of frontotemporal lobar degeneration (ftld) cases. |
2022-10-27 |
2023-08-14 |
Not clear |