| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Ramona Meanti, Martina Licata, Laura Rizzi, Elena Bresciani, Laura Molteni, Silvia Coco, Vittorio Locatelli, Robert J Omeljaniuk, Antonio Torsell. Protective Effects of Hexarelin and JMV2894 in a Human Neuroblastoma Cell Line Expressing the SOD1-G93A Mutated Protein. International journal of molecular sciences. vol 24. issue 2. 2023-01-21. PMID:36674509. |
amyotrophic lateral sclerosis (als) is an incurable motor neuron disease whose etiology remains unresolved; nonetheless, mutations of superoxide dismutase 1 (sod1) have been associated with several variants of als. |
2023-01-21 |
2023-08-14 |
human |
| H Li, L Yuan, H Yang, Y Guo, W Zheng, K Fan, S Deng, L Gong, H Xu, Z Yang, J Cheng, M Kang, H Den. Analysis of SOD1 Variants in Chinese Patients with Familial Amyotrophic Lateral Sclerosis. QJM : monthly journal of the Association of Physicians. 2023-01-20. PMID:36661322. |
analysis of sod1 variants in chinese patients with familial amyotrophic lateral sclerosis. |
2023-01-20 |
2023-08-14 |
Not clear |
| Siyu Gu, Ming Xu, Long Chen, Xiangyan Shi, Shi-Zhong Lu. A liquid-to-solid phase transition of Cu/Zn superoxide dismutase 1(SOD1)initiated by oxidation and disease mutation. The Journal of biological chemistry. 2023-01-02. PMID:36592929. |
cu/zn superoxide dismutase 1 (sod1) has a high propensity to misfold and form abnormal aggregates when it is subjected to oxidative stress or carries mutations associated with amyotrophic lateral sclerosis. |
2023-01-02 |
2023-08-14 |
Not clear |
| 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 |
| Yingzhen Zhang, Lin Chen, Zhongzhong Li, Dongxiao Li, Yue Wu, Yansu Gu. Endothelin-1, over-expressed in SOD1 Frontiers in cellular neuroscience. vol 16. 2022-12-19. PMID:36531135. |
endothelin-1, over-expressed in sod1 endothelin-1 (et-1), a secreted signaling peptide, is suggested to be involved in multiple actions in various tissues including the brain, but its role in amyotrophic lateral sclerosis (als) remains unknown. |
2022-12-19 |
2023-08-14 |
mouse |
| Shan Jin, Zhengzhe Sun, Xiang Fang, Huaizhen Chen, Wenming Yan. A patient carrying a heterozygous p.Asn267Ser TARDBP missense mutation diagnosed as ALS and only involving lower motor neurons. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2022-12-17. PMID:36527522. |
amyotrophic lateral sclerosis (als) is a rare neurodegenerative disease involving upper motor neurons (umn) and lower motor neurons (lmn), which can be caused by mutations of pathogenic genes such as superoxide dismutase 1 (sod1), sarcoma fusion (fus), and tar-dna binding protein (tarbdp/tdp-43). |
2022-12-17 |
2023-08-14 |
Not clear |
| Siyue Qin, Pan You, Hui Yu, Bo S. REEP1 Preserves Motor Function in SOD1 Neuroscience bulletin. 2022-12-15. PMID:36520405. |
reep1 preserves motor function in sod1 a decline in the activities of oxidative phosphorylation (oxphos) complexes has been consistently reported in amyotrophic lateral sclerosis (als) patients and animal models of als, although the underlying molecular mechanisms are still elusive. |
2022-12-15 |
2023-08-14 |
Not clear |
| C F Cavarsan, P R Steele, L T Genry, E J Reedich, L M McCane, K J LaPre, A C Puritz, M Manuel, N Katenka, K A Quinla. Inhibitory interneurons show early dysfunction in a SOD1 mouse model of amyotrophic lateral sclerosis. The Journal of physiology. 2022-12-14. PMID:36515374. |
inhibitory interneurons show early dysfunction in a sod1 mouse model of amyotrophic lateral sclerosis. |
2022-12-14 |
2023-08-14 |
mouse |
| Jimena Jaramillo, Juan M Solano, Alejandra Aristizábal, Juliana Martíne. Analysis of SOD1 and C9orf72 mutations in patients with amyotrophic lateral sclerosis in Antioquia, Colombia. Biomedica : revista del Instituto Nacional de Salud. vol 42. issue 4. 2022-12-13. PMID:36511680. |
analysis of sod1 and c9orf72 mutations in patients with amyotrophic lateral sclerosis in antioquia, colombia. |
2022-12-13 |
2023-08-14 |
Not clear |
| Feng Gao, Jingyi Sun, Minmin Yao, Yanan Song, Hui Yi, Mingfeng Yang, Qingbin Ni, Jiming Kong, Hui Yuan, Baoliang Sun, Ying Wan. SERS "hot spot" enhance-array assay for misfolded SOD1 correlated with white matter lesions and aging. Analytica chimica acta. vol 1238. 2022-12-04. PMID:36464456. |
misfolding of superoxide dismutase-1 (sod1) has been correlated with many neurodegenerative diseases, such as amyotrophic lateral sclerosis's and alzheimer's among others. |
2022-12-04 |
2023-08-14 |
Not clear |
| Shaherin Basith, Balachandran Manavalan, Gwang Le. Amyotrophic lateral sclerosis disease-related mutations disrupt the dimerization of superoxide dismutase 1 - A comparative molecular dynamics simulation study. Computers in biology and medicine. vol 151. issue Pt B. 2022-11-29. PMID:36446187. |
more than 150 genes are involved in amyotrophic lateral sclerosis (als), with superoxide dismutase 1 (sod1) being one of the most studied. |
2022-11-29 |
2023-08-14 |
Not clear |
| Anastasia Sarikidi, Ekaterini Kefalakes, Christine S Falk, Ruth Esser, Arnold Ganser, Nadine Thau-Habermann, Susanne Petr. Altered Immunomodulatory Responses in the CX3CL1/CX3CR1 Axis Mediated by hMSCs in an Early In Vitro SOD1 Biomedicines. vol 10. issue 11. 2022-11-26. PMID:36428484. |
altered immunomodulatory responses in the cx3cl1/cx3cr1 axis mediated by hmscs in an early in vitro sod1 amyotrophic lateral sclerosis (als) is a fatal motor neuron (mn) disease characterized by progressive mn loss and muscular atrophy resulting in rapidly progressive paralysis and respiratory failure. |
2022-11-26 |
2023-08-14 |
human |
| Bidisha Das, Sumangal Roychowdhury, Priyesh Mohanty, Azamat Rizuan, Joy Chakraborty, Jeetain Mittal, Krishnananda Chattopadhya. A Zn-dependent structural transition of SOD1 modulates its ability to undergo phase separation. The EMBO journal. 2022-11-23. PMID:36416085. |
the misfolding and mutation of cu/zn superoxide dismutase (sod1) is commonly associated with amyotrophic lateral sclerosis (als). |
2022-11-23 |
2023-08-14 |
Not clear |
| Xiawei Dang, Lihong Zhang, Antonietta Franco, Gerald W Dor. Activating mitofusins interrupts mitochondrial degeneration and delays disease progression in SOD1 mutant amyotrophic lateral sclerosis. Human molecular genetics. 2022-11-23. PMID:36416308. |
activating mitofusins interrupts mitochondrial degeneration and delays disease progression in sod1 mutant amyotrophic lateral sclerosis. |
2022-11-23 |
2023-08-14 |
mouse |
| Xiawei Dang, Lihong Zhang, Antonietta Franco, Gerald W Dor. Activating mitofusins interrupts mitochondrial degeneration and delays disease progression in SOD1 mutant amyotrophic lateral sclerosis. Human molecular genetics. 2022-11-23. PMID:36416308. |
can enhanced mitochondrial fusion and motility improve secondary mitochondrial pathology in sod1 mutant amyotrophic lateral sclerosis (als)? |
2022-11-23 |
2023-08-14 |
mouse |
| Karin M Forsberg, Karin S Graffmo, Erica Stenvall, Naima Tabikh, Stefan L Marklund, Thomas Brännström, Peter M Anderse. Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation. Acta neuropathologica. 2022-11-17. PMID:36385230. |
widespread cns pathology in amyotrophic lateral sclerosis homozygous for the d90a sod1 mutation. |
2022-11-17 |
2023-08-14 |
Not clear |
| Karin M Forsberg, Karin S Graffmo, Erica Stenvall, Naima Tabikh, Stefan L Marklund, Thomas Brännström, Peter M Anderse. Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation. Acta neuropathologica. 2022-11-17. PMID:36385230. |
mutations in the gene encoding the ubiquitously expressed free radical scavenging enzyme superoxide dismutase-1 (sod1) are found in 2-6% of amyotrophic lateral sclerosis patients. |
2022-11-17 |
2023-08-14 |
Not clear |
| Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, Olubunmi Abel, Keith Mayl, Puja R Mehta, Aleksey Shatunov, Isabella Fogh, Harry Bowles, Naomi Limbachiya, Thomas P Spargo, Ahmad Al-Khleifat, Kelly L Williams, Jennifer Jockel-Balsarotti, Taha Bali, Wade Self, Lyndal Henden, Garth A Nicholson, Nicola Ticozzi, Diane McKenna-Yasek, Lu Tang, Pamela J Shaw, Adriano Chio, Albert Ludolph, Jochen H Weishaupt, John E Landers, Jonathan D Glass, Jesus S Mora, Wim Robberecht, Philip Van Damme, Russell McLaughlin, Orla Hardiman, Leonard van den Berg, Jan H Veldink, Phillippe Corcia, Zorica Stevic, Nailah Siddique, Vincenzo Silani, Ian P Blair, Dong-Sheng Fan, Florence Esselin, Elisa de la Cruz, William Camu, Nazli A Basak, Teepu Siddique, Timothy Miller, Robert H Brown, Ammar Al-Chalabi, Christopher E Sha. The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration. Nature communications. vol 13. issue 1. 2022-11-13. PMID:36371497. |
superoxide dismutase (sod1) gene variants may cause amyotrophic lateral sclerosis, some of which are associated with a distinct phenotype. |
2022-11-13 |
2023-08-14 |
Not clear |
| Xinyu Bian, Xiaoyu Zhuang, Junpeng Xing, Shu Liu, Zhiqiang Liu, Fengrui Son. Native Mass Spectrometry Coupled to Spectroscopic Methods to Investigate the Effect of Soybean Isoflavones on Structural Stability and Aggregation of Zinc Deficient and Metal-Free Superoxide Dismutase. Molecules (Basel, Switzerland). vol 27. issue 21. 2022-11-11. PMID:36364128. |
the deficiency or wrong combination of metal ions in cu, zn-superoxide dismutase (sod1), is regarded as one of the main factors causing the aggregation of sod1 and then inducing amyotrophic lateral sclerosis (als). |
2022-11-11 |
2023-08-14 |
Not clear |
| Chad M Dashnaw, Ao Yun Zhang, Mayte Gonzalez, Jordan C Koone, Bryan F Sha. Metal migration and subunit swapping in ALS-linked SOD1: Zn The Journal of biological chemistry. 2022-10-20. PMID:36265587. |
metal migration and subunit swapping in als-linked sod1: zn the heterodimerization of wild-type (wt) cu, zn superoxide dismutase-1 (sod1) and mutant sod1 might be a critical step in the pathogenesis of sod1-linked amyotrophic lateral sclerosis (als). |
2022-10-20 |
2023-08-14 |
Not clear |