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Frontiers | Human Motor Neurons With SOD1-G93A Mutation Generated From  CRISPR/Cas9 Gene-Edited iPSCs Develop Pathological Features of Amyotrophic  Lateral Sclerosis
Frontiers | Human Motor Neurons With SOD1-G93A Mutation Generated From CRISPR/Cas9 Gene-Edited iPSCs Develop Pathological Features of Amyotrophic Lateral Sclerosis

SOD1/Rag2 Mice with Low Copy Number of SOD1 Gene as a New Long-Living  Immunodeficient Model of ALS | Scientific Reports
SOD1/Rag2 Mice with Low Copy Number of SOD1 Gene as a New Long-Living Immunodeficient Model of ALS | Scientific Reports

Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological  deficits with severe mitochondrial pathology | PNAS
Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology | PNAS

ALS-Linked SOD1 Mutant G85R Mediates Damage to Astrocytes and Promotes  Rapidly Progressive Disease with SOD1-Containing Inclusions: Neuron
ALS-Linked SOD1 Mutant G85R Mediates Damage to Astrocytes and Promotes Rapidly Progressive Disease with SOD1-Containing Inclusions: Neuron

Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in  ALS Mice | Science
Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice | Science

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

Characterization of somatosensory neuron involvement in the SOD1G93A mouse  model | Scientific Reports
Characterization of somatosensory neuron involvement in the SOD1G93A mouse model | Scientific Reports

Transgenic mice expressing H46R/H48Q/H63G/H120G (Quad) mutant SOD1... |  Download Scientific Diagram
Transgenic mice expressing H46R/H48Q/H63G/H120G (Quad) mutant SOD1... | Download Scientific Diagram

Generation and analysis of innovative genomically humanized knockin SOD1,  TARDBP (TDP-43), and FUS mouse models - ScienceDirect
Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models - ScienceDirect

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

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

Preliminary Observation about Alteration of Proteins and Their Potential  Functions in Spinal Cord of SOD1 G93A Transgenic Mice
Preliminary Observation about Alteration of Proteins and Their Potential Functions in Spinal Cord of SOD1 G93A Transgenic Mice

SOD1-G93A Mouse Model - QPS Neuropharmacology
SOD1-G93A Mouse Model - QPS Neuropharmacology

Figure 3.1 from The neuromuscular transmission of the SOD 1 ( G 93 A ) mouse  model of Amyotrophic Lateral Sclerosis | Semantic Scholar
Figure 3.1 from The neuromuscular transmission of the SOD 1 ( G 93 A ) mouse model of Amyotrophic Lateral Sclerosis | Semantic Scholar

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

PDF] Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1  mouse. | Semantic Scholar
PDF] Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouse. | Semantic Scholar

ALS-Linked SOD1 Mutants Enhance Neurite Outgrowth and Branching in Adult  Motor Neurons
ALS-Linked SOD1 Mutants Enhance Neurite Outgrowth and Branching in Adult Motor Neurons

Frontiers | Skeletal Muscle-Restricted Expression of Human SOD1 in  Transgenic Mice Causes a Fatal ALS-Like Syndrome
Frontiers | Skeletal Muscle-Restricted Expression of Human SOD1 in Transgenic Mice Causes a Fatal ALS-Like Syndrome

004435 - SOD1-G93A Strain Details
004435 - SOD1-G93A Strain Details

Optimised and Rapid Pre-clinical Screening in the SOD1G93A Transgenic Mouse  Model of Amyotrophic Lateral Sclerosis (ALS) | PLOS ONE
Optimised and Rapid Pre-clinical Screening in the SOD1G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis (ALS) | PLOS ONE

Novel chemical inhibitor against SOD1 misfolding and aggregation protects  neuron-loss and ameliorates disease symptoms in ALS mouse model |  Communications Biology
Novel chemical inhibitor against SOD1 misfolding and aggregation protects neuron-loss and ameliorates disease symptoms in ALS mouse model | Communications Biology

The Loss of TBK1 Kinase Activity in Motor Neurons or in All Cell Types  Differentially Impacts ALS Disease Progression in SOD1 Mice - ScienceDirect
The Loss of TBK1 Kinase Activity in Motor Neurons or in All Cell Types Differentially Impacts ALS Disease Progression in SOD1 Mice - ScienceDirect

General behavior of SOD1 G93A mice. (A) Body weight variations in... |  Download Scientific Diagram
General behavior of SOD1 G93A mice. (A) Body weight variations in... | Download Scientific Diagram

Parkin is a disease modifier in the mutant SOD1 mouse model of ALS | EMBO  Molecular Medicine
Parkin is a disease modifier in the mutant SOD1 mouse model of ALS | EMBO Molecular Medicine

Decreasing SOD1 in muscle does not improve grip strength in SOD1 G93A... |  Download Scientific Diagram
Decreasing SOD1 in muscle does not improve grip strength in SOD1 G93A... | Download Scientific Diagram