Articles with "sca1" as a keyword



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Polarization-sensitive optical coherence tomography reveals gray matter and white matter atrophy in SCA1 mouse models

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Published in 2018 at "Neurobiology of Disease"

DOI: 10.1016/j.nbd.2018.05.003

Abstract: Spinocerebellar ataxia type 1 (SCA1) is a fatal inherited neurodegenerative disease. In this study, we demonstrate the label-free optical imaging methodology that can detect, with a high degree of sensitivity, discrete areas of degeneration in… read more here.

Keywords: sca1; matter; gray matter; matter atrophy ... See more keywords

P14.102 Cerebellar atrophy patterns in paraneoplastic cerebellar degeneraiton and spinocerebellar ataxia 1 (SCA1)

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Published in 2019 at "Neuro-Oncology"

DOI: 10.1093/neuonc/noz126.337

Abstract: Brain and more specifically cerebellar atrophy is a major radiological finding in both Paraneoplastic Cerebellar Degeneration (PCD) with anti-Yo antibodies and Spinocerebellar Ataxia type 1 (SCA1).We sought to analyze the different brain volumetric patterns of… read more here.

Keywords: paraneoplastic cerebellar; spinocerebellar ataxia; sca1; pcd ... See more keywords
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Adventitial Sca1+ Cells Transduced With ETV2 Are Committed to the Endothelial Fate and Improve Vascular Remodeling After Injury

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Published in 2018 at "Arteriosclerosis, Thrombosis, and Vascular Biology"

DOI: 10.1161/atvbaha.117.309853

Abstract: Objective— Vascular adventitial Sca1+ (stem cell antigen-1) progenitor cells preferentially differentiate into smooth muscle cells, which contribute to vascular remodeling and neointima formation in vessel grafts. Therefore, directing the differentiation of Sca1+ cells toward the… read more here.

Keywords: endothelial fate; sca1; sca1 cells; adventitial sca1 ... See more keywords
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Therapeutic Strategies for Spinocerebellar Ataxia Type 1

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Published in 2023 at "Biomolecules"

DOI: 10.3390/biom13050788

Abstract: Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disorder that affects one or two individuals per 100,000. The disease is caused by an extended CAG repeat in exon 8 of the ATXN1 gene… read more here.

Keywords: therapeutic strategies; sca1; ataxia type; strategies spinocerebellar ... See more keywords
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Genetic Modeling of the Neurodegenerative Disease Spinocerebellar Ataxia Type 1 in Zebrafish

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Published in 2021 at "International Journal of Molecular Sciences"

DOI: 10.3390/ijms22147351

Abstract: Dominant spinocerebellar ataxias (SCAs) are progredient neurodegenerative diseases commonly affecting the survival of Purkinje cells (PCs) in the human cerebellum. Spinocerebellar ataxia type 1 (SCA1) is caused by the mutated ataxin1 (Atx1) gene product, in… read more here.

Keywords: ataxia type; spinocerebellar ataxia; sca1; disease ... See more keywords