![IJMS | Free Full-Text | Therapeutic Treatment of Superoxide Dismutase 1 ( G93A) Amyotrophic Lateral Sclerosis Model Mice with Medical Ozone Decelerates Trigeminal Motor Neuron Degeneration, Attenuates Microglial Proliferation, and Preserves Monocyte Levels IJMS | Free Full-Text | Therapeutic Treatment of Superoxide Dismutase 1 ( G93A) Amyotrophic Lateral Sclerosis Model Mice with Medical Ozone Decelerates Trigeminal Motor Neuron Degeneration, Attenuates Microglial Proliferation, and Preserves Monocyte Levels](https://pub.mdpi-res.com/ijms/ijms-23-03403/article_deploy/html/images/ijms-23-03403-g001.png?1647933352)
IJMS | Free Full-Text | Therapeutic Treatment of Superoxide Dismutase 1 ( G93A) Amyotrophic Lateral Sclerosis Model Mice with Medical Ozone Decelerates Trigeminal Motor Neuron Degeneration, Attenuates Microglial Proliferation, and Preserves Monocyte Levels
![Neuroprotective effects of siRNAp11 in the SOD1-G93A mouse model of... | Download Scientific Diagram Neuroprotective effects of siRNAp11 in the SOD1-G93A mouse model of... | Download Scientific Diagram](https://www.researchgate.net/publication/335321624/figure/fig4/AS:958965122863115@1605646510407/Neuroprotective-effects-of-siRNAp11-in-the-SOD1-G93A-mouse-model-of-ALS-a-In-situ.png)
Neuroprotective effects of siRNAp11 in the SOD1-G93A mouse model of... | Download Scientific Diagram
Optimised and Rapid Pre-clinical Screening in the SOD1G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis (ALS) | PLOS ONE
![Targeting autotaxin impacts disease advance in the SOD1‐G93A mouse model of amyotrophic lateral sclerosis - Gento‐Caro - 2022 - Brain Pathology - Wiley Online Library Targeting autotaxin impacts disease advance in the SOD1‐G93A mouse model of amyotrophic lateral sclerosis - Gento‐Caro - 2022 - Brain Pathology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/20d3e233-bb72-42cd-ba86-9067d33d1efb/bpa13022-fig-0004-m.jpg)
Targeting autotaxin impacts disease advance in the SOD1‐G93A mouse model of amyotrophic lateral sclerosis - Gento‐Caro - 2022 - Brain Pathology - Wiley Online Library
![Amelioration of Amyotrophic Lateral Sclerosis in SOD1G93A Mice by M2 Microglia from Transplanted Marrow | In Vivo Amelioration of Amyotrophic Lateral Sclerosis in SOD1G93A Mice by M2 Microglia from Transplanted Marrow | In Vivo](https://iv.iiarjournals.org/content/invivo/33/3/675/F2.large.jpg?width=800&height=600&carousel=1)
Amelioration of Amyotrophic Lateral Sclerosis in SOD1G93A Mice by M2 Microglia from Transplanted Marrow | In Vivo
![Delayed Disease Onset and Extended Survival in the SOD1G93A Rat Model of Amyotrophic Lateral Sclerosis after Suppression of Mutant SOD1 in the Motor Cortex | Journal of Neuroscience Delayed Disease Onset and Extended Survival in the SOD1G93A Rat Model of Amyotrophic Lateral Sclerosis after Suppression of Mutant SOD1 in the Motor Cortex | Journal of Neuroscience](https://www.jneurosci.org/content/jneuro/34/47/15587/F4.large.jpg)
Delayed Disease Onset and Extended Survival in the SOD1G93A Rat Model of Amyotrophic Lateral Sclerosis after Suppression of Mutant SOD1 in the Motor Cortex | Journal of Neuroscience
![Frontiers | Neuroprotective Effects of Shenqi Fuzheng Injection in a Transgenic SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis Frontiers | Neuroprotective Effects of Shenqi Fuzheng Injection in a Transgenic SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis](https://www.frontiersin.org/files/Articles/701886/fphar-12-701886-HTML/image_m/fphar-12-701886-g001.jpg)
Frontiers | Neuroprotective Effects of Shenqi Fuzheng Injection in a Transgenic SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis
![Microglia and motor neurons during disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis: changes in arginase1 and inducible nitric oxide synthase | Journal of Neuroinflammation | Full Text Microglia and motor neurons during disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis: changes in arginase1 and inducible nitric oxide synthase | Journal of Neuroinflammation | Full Text](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2F1742-2094-11-55/MediaObjects/12974_2013_Article_984_Fig7_HTML.jpg)
Microglia and motor neurons during disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis: changes in arginase1 and inducible nitric oxide synthase | Journal of Neuroinflammation | Full Text
![Neuroprotective Effects of Genistein in a SOD1-G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis | Journal of Neuroimmune Pharmacology Neuroprotective Effects of Genistein in a SOD1-G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis | Journal of Neuroimmune Pharmacology](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs11481-019-09866-x/MediaObjects/11481_2019_9866_Fig5_HTML.png)
Neuroprotective Effects of Genistein in a SOD1-G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis | Journal of Neuroimmune Pharmacology
![Motor neuronal protection by l-arginine prolongs survival of mutant SOD1 ( G93A) ALS mice - ScienceDirect Motor neuronal protection by l-arginine prolongs survival of mutant SOD1 ( G93A) ALS mice - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0006291X0900905X-gr3.jpg)
Motor neuronal protection by l-arginine prolongs survival of mutant SOD1 ( G93A) ALS mice - ScienceDirect
![Neuroprotective Effects of Genistein in a SOD1-G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis | Journal of Neuroimmune Pharmacology Neuroprotective Effects of Genistein in a SOD1-G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis | Journal of Neuroimmune Pharmacology](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs11481-019-09866-x/MediaObjects/11481_2019_9866_Fig1_HTML.png)
Neuroprotective Effects of Genistein in a SOD1-G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis | Journal of Neuroimmune Pharmacology
![Biomedicines | Free Full-Text | Intrathecal Injection of the Secretome from ALS Motor Neurons Regulated for miR-124 Expression Prevents Disease Outcomes in SOD1-G93A Mice Biomedicines | Free Full-Text | Intrathecal Injection of the Secretome from ALS Motor Neurons Regulated for miR-124 Expression Prevents Disease Outcomes in SOD1-G93A Mice](https://www.mdpi.com/biomedicines/biomedicines-10-02120/article_deploy/html/images/biomedicines-10-02120-g001.png)
Biomedicines | Free Full-Text | Intrathecal Injection of the Secretome from ALS Motor Neurons Regulated for miR-124 Expression Prevents Disease Outcomes in SOD1-G93A Mice
![CuATSM improves motor function and extends survival but is not tolerated at a high dose in SOD1G93A mice with a C57BL/6 background | Scientific Reports CuATSM improves motor function and extends survival but is not tolerated at a high dose in SOD1G93A mice with a C57BL/6 background | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-021-98317-w/MediaObjects/41598_2021_98317_Fig1_HTML.png)
CuATSM improves motor function and extends survival but is not tolerated at a high dose in SOD1G93A mice with a C57BL/6 background | Scientific Reports
Decreasing SOD1 in muscle does not improve grip strength in SOD1 G93A... | Download Scientific Diagram
![Frontiers | Evaluation of Neuropathological Features in the SOD1-G93A Low Copy Number Transgenic Mouse Model of Amyotrophic Lateral Sclerosis Frontiers | Evaluation of Neuropathological Features in the SOD1-G93A Low Copy Number Transgenic Mouse Model of Amyotrophic Lateral Sclerosis](https://www.frontiersin.org/files/MyHome%20Article%20Library/681868/681868_Thumb_400.jpg)
Frontiers | Evaluation of Neuropathological Features in the SOD1-G93A Low Copy Number Transgenic Mouse Model of Amyotrophic Lateral Sclerosis
![Neuron-Specific Expression of Mutant Superoxide Dismutase Is Sufficient to Induce Amyotrophic Lateral Sclerosis in Transgenic Mice | Journal of Neuroscience Neuron-Specific Expression of Mutant Superoxide Dismutase Is Sufficient to Induce Amyotrophic Lateral Sclerosis in Transgenic Mice | Journal of Neuroscience](https://www.jneurosci.org/content/jneuro/28/9/2075/F1.large.jpg?width=800&height=600&carousel=1)
Neuron-Specific Expression of Mutant Superoxide Dismutase Is Sufficient to Induce Amyotrophic Lateral Sclerosis in Transgenic Mice | Journal of Neuroscience
![Simvastatin accelerated motoneurons death in SOD1G93A mice through inhibiting Rab7-mediated maturation of late autophagic vacuoles | Cell Death & Disease Simvastatin accelerated motoneurons death in SOD1G93A mice through inhibiting Rab7-mediated maturation of late autophagic vacuoles | Cell Death & Disease](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41419-021-03669-w/MediaObjects/41419_2021_3669_Fig1_HTML.png)
Simvastatin accelerated motoneurons death in SOD1G93A mice through inhibiting Rab7-mediated maturation of late autophagic vacuoles | Cell Death & Disease
![Neuroprotective effects of the cannabigerol quinone derivative VCE-003.2 in SOD1G93A transgenic mice, an experimental model of amyotrophic lateral sclerosis - ScienceDirect Neuroprotective effects of the cannabigerol quinone derivative VCE-003.2 in SOD1G93A transgenic mice, an experimental model of amyotrophic lateral sclerosis - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0006295218303198-ga1.jpg)
Neuroprotective effects of the cannabigerol quinone derivative VCE-003.2 in SOD1G93A transgenic mice, an experimental model of amyotrophic lateral sclerosis - ScienceDirect
![A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis | Science Translational Medicine A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis | Science Translational Medicine](https://www.science.org/cms/10.1126/scitranslmed.aah3924/asset/28b80e18-c1a3-4fc9-a6dc-5be95f80d085/assets/graphic/aah3924-f2.jpeg)