Cargando…
Bioinformatics Data Mining Approach Suggests Coexpression of AGTPBP1 with an ALS-linked Gene C9orf72
BACKGROUND: Expanded GGGGCC hexanucleotide repeats located in the noncoding region of the chromosome 9 open reading frame 72 (C9orf72) gene represent the most common genetic abnormality for familial and sporadic amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Formation of nucl...
Autores principales: | Kitano, Shouta, Kino, Yoshihiro, Yamamoto, Yoji, Takitani, Mika, Miyoshi, Junko, Ishida, Tsuyoshi, Saito, Yuko, Arima, Kunimasa, Satoh, Jun-ichi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467204/ https://www.ncbi.nlm.nih.gov/pubmed/26106267 http://dx.doi.org/10.4137/JCNSD.S24317 |
Ejemplares similares
-
Molecular Network Analysis Suggests a Logical Hypothesis for the Pathological Role of C9orf72 in Amyotrophic Lateral Sclerosis/Frontotemporal Dementia
por: Satoh, Jun-ichi, et al.
Publicado: (2014) -
Dystrophic neurites express C9orf72 in Alzheimer's disease brains
por: Satoh, Jun-ichi, et al.
Publicado: (2012) -
TMEM106B expression is reduced in Alzheimer’s disease brains
por: Satoh, Jun-ichi, et al.
Publicado: (2014) -
PLD3 is accumulated on neuritic plaques in Alzheimer’s disease brains
por: Satoh, Jun-ichi, et al.
Publicado: (2014) -
A Comprehensive Profile of ChIP-Seq-Based Olig2 Target Genes in Motor Neuron Progenitor Cells Suggests the Possible Involvement of Olig2 in the Pathogenesis of Amyotrophic Lateral Sclerosis
por: Satoh, Jun-ichi, et al.
Publicado: (2015)