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Search Results - c9orf72
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Mouse Model of
C9orf72
that Develops the Clinical and Neurodegenerative Features of Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD)
Recapitulates Features of ALS and FTD using a Patient Derived Human TransgeneExpansion of the number of repeats of a specific hexanucleotide sequence (GGGGCC, called G4C2) in the
C9orf72
gene is the most common known cause of Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD). This C9-500 mouse model contains a mutation with 500 G4C2...
Published: 6/27/2021
|
Inventor(s):
Laura Ranum
Keywords(s):
Amyotrophic lateral sclerosis (ALS)
,
C9ORF72
,
C9ORF72
BAC mouse model
,
Frontotemporal Dementia (FTD)
,
repeat associated non-ATG (RAN)-Translation
Category(s):
Technology Classifications > Research Tools > Others