Pub. Date : 2013
PMID : 24455732
5 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Presymptomatic treatment with acetylcholinesterase antisense oligonucleotides prolongs survival in ALS (G93A-SOD1) mice. | Oligonucleotides | acetylcholinesterase | Mus musculus |
2 | AChE enzyme inhibitors can upregulate AChE transcription which in certain contexts can have deleterious (noncatalytic) effects, making them theoretically harmful in ALS, whilst AChE antisense-oligonucleotides (mEN101), which downregulate AChE may be beneficial. | Oligonucleotides | acetylcholinesterase | Mus musculus |
3 | AChE enzyme inhibitors can upregulate AChE transcription which in certain contexts can have deleterious (noncatalytic) effects, making them theoretically harmful in ALS, whilst AChE antisense-oligonucleotides (mEN101), which downregulate AChE may be beneficial. | Oligonucleotides | acetylcholinesterase | Mus musculus |
4 | AChE enzyme inhibitors can upregulate AChE transcription which in certain contexts can have deleterious (noncatalytic) effects, making them theoretically harmful in ALS, whilst AChE antisense-oligonucleotides (mEN101), which downregulate AChE may be beneficial. | Oligonucleotides | acetylcholinesterase | Mus musculus |
5 | AChE enzyme inhibitors can upregulate AChE transcription which in certain contexts can have deleterious (noncatalytic) effects, making them theoretically harmful in ALS, whilst AChE antisense-oligonucleotides (mEN101), which downregulate AChE may be beneficial. | Oligonucleotides | acetylcholinesterase | Mus musculus |