Selective C9orf72 G-Quadruplex-Binding Small Molecules Ameliorate Pathological Signatures of ALS/FTD Models

A Cheng, C Liu, W Ye, D Huang, W She… - Journal of Medicinal …, 2022 - ACS Publications
The G-quadruplex (G4) forming C9orf72 GGGGCC (G4C2) expanded hexanucleotide repeat
(EHR) is the predominant genetic cause of amyotrophic lateral sclerosis (ALS) and …

[PDF][PDF] Selective C9orf 72 G‑Quadruplex-Binding Small Molecules Ameliorate Pathological Signatures of ALS/FTD Models

researchgate.net
The G-quadruplex (G4) forming C9orf 72 GGGGCC (G4C2) expanded hexanucleotide
repeat (EHR) is the predominant genetic cause of amyotrophic lateral sclerosis (ALS) and …

[HTML][HTML] Selective C9orf72 G-Quadruplex-Binding Small Molecules Ameliorate Pathological Signatures of ALS/FTD Models

A Cheng, C Liu, W Ye, D Huang, W She… - Journal of Medicinal …, 2022 - ncbi.nlm.nih.gov
The G-quadruplex (G4) forming C9orf 72 GGGGCC (G4C2) expanded hexanucleotide
repeat (EHR) is the predominant genetic cause of amyotrophic lateral sclerosis (ALS) and …

Selective C9orf72 G-Quadruplex-Binding Small Molecules Ameliorate Pathological Signatures of ALS/FTD Models.

A Cheng, C Liu, W Ye, D Huang, W She… - Journal of Medicinal …, 2022 - europepmc.org
The G-quadruplex (G4) forming C9orf 72 GGGGCC (G4C2) expanded hexanucleotide
repeat (EHR) is the predominant genetic cause of amyotrophic lateral sclerosis (ALS) and …

Selective C9orf72 G-Quadruplex-Binding Small Molecules Ameliorate Pathological Signatures of ALS/FTD Models

A Cheng, C Liu, W Ye, D Huang… - Journal of …, 2022 - pubmed.ncbi.nlm.nih.gov
The G-quadruplex (G4) forming C9orf72 GGGGCC (G4C2) expanded hexanucleotide repeat
(EHR) is the predominant genetic cause of amyotrophic lateral sclerosis (ALS) and …

Selective C9orf72 G-Quadruplex-Binding Small Molecules Ameliorate Pathological Signatures of ALS/FTD Models.

A Cheng, C Liu, W Ye, D Huang, W She… - Journal of Medicinal …, 2022 - europepmc.org
The G-quadruplex (G4) forming C9orf72 GGGGCC (G4C2) expanded hexanucleotide repeat
(EHR) is the predominant genetic cause of amyotrophic lateral sclerosis (ALS) and …