International audienceA variety of missense mutations and a stop mutation in the gene coding for transmembrane protein 240 (TMEM240) have been reported to be the causative mutations of spinocerebellar ataxia 21 (SCA21). We aimed to investigate the expression of TMEM240 protein in mouse brain at the tissue, cellular, and subcellular levels. Immunofluorescence labeling showed TMEM240 to be expressed in various areas of the brain, with the highest levels in the hippocampus, isocortex, and cerebellum. In the cerebellum, TMEM240 was detected in the deep nuclei and the cerebellar cortex. The protein was expressed in all three layers of the cortex and various cerebellar neurons. TMEM240 was localized to climbing, mossy, and parallel fiber afferent...
Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotemporal dement...
The structural microtubule-associated proteins (MAPs) are critical for the organization of neuronal ...
Abstract Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotempor...
International audienceA variety of missense mutations and a stop mutation in the gene coding for tra...
International audienceA variety of missense mutations and a stop mutation in the gene coding for tra...
International audienceAutosomal dominant cerebellar ataxia corresponds to a clinically and genetical...
Abstract Phospholipids are asymmetrically distributed across mammalian plasma membrane with phosphat...
The cerebellum (Latin for “little brain”) is a region of the brain that plays an important role in r...
Parkinson's disease is the second most common neurodegenerative disorder without effective treatment...
Abstract Background p23 belongs to the highly conserved p24 family of type I transmembrane proteins,...
To elucidate the novel molecular cause in families with a new autosomal recessive neurodevelopmental...
REPORT TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitiv...
Spinocerebellar ataxia type 6 (SCA6) is linked to poly-glutamine (polyQ) within the C terminus (CT) ...
Transmembrane protein 50b, Tmem50b, previously referred to as C21orf4, encodes a predicted transmemb...
Purkinje neurons are a sensitive and specialised cell type important for fine motor movement and coo...
Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotemporal dement...
The structural microtubule-associated proteins (MAPs) are critical for the organization of neuronal ...
Abstract Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotempor...
International audienceA variety of missense mutations and a stop mutation in the gene coding for tra...
International audienceA variety of missense mutations and a stop mutation in the gene coding for tra...
International audienceAutosomal dominant cerebellar ataxia corresponds to a clinically and genetical...
Abstract Phospholipids are asymmetrically distributed across mammalian plasma membrane with phosphat...
The cerebellum (Latin for “little brain”) is a region of the brain that plays an important role in r...
Parkinson's disease is the second most common neurodegenerative disorder without effective treatment...
Abstract Background p23 belongs to the highly conserved p24 family of type I transmembrane proteins,...
To elucidate the novel molecular cause in families with a new autosomal recessive neurodevelopmental...
REPORT TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitiv...
Spinocerebellar ataxia type 6 (SCA6) is linked to poly-glutamine (polyQ) within the C terminus (CT) ...
Transmembrane protein 50b, Tmem50b, previously referred to as C21orf4, encodes a predicted transmemb...
Purkinje neurons are a sensitive and specialised cell type important for fine motor movement and coo...
Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotemporal dement...
The structural microtubule-associated proteins (MAPs) are critical for the organization of neuronal ...
Abstract Hexanucleotide repeat expansion in C9orf72 is the most common genetic cause of frontotempor...