Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Na Young Yang"'
Publikováno v:
bchm. 394:807-818
Mutations in the gene encoding glucocerebrosidase (GBA1) cause Gaucher disease (GD), a lysosomal storage disease with recessive inheritance. Glucocerebrosidase (GCase) is a lysosomal lipid hydrolase that digests glycolipid substrates, such as glucosy
Autor:
Na-young Yang
Publikováno v:
Journal of Human Environmental Studies. 6:73-78
Autor:
Mi-Young Song, Seokjoong Kim, Seung-Jae Lee, Eliezer Masliah, Byung Chul Jung, Jun Sung Lee, Na Young Yang, He Jin Lee, Sergio Pablo Sardi, Eun Jin Bae, Cheol Soon Lee
Publikováno v:
NATURE COMMUNICATIONS(5)
Deposition of alpha-synuclein aggregates occurs widely in the central and peripheral nervous systems in Parkinson's disease (PD). Although recent evidence has suggested that cell-to-cell transmission of alpha-synuclein aggregates is associated with t
Autor:
He Jin Lee, Na Young Yang, Eun Bi Park, Eun Jin Bae, Edward Rockenstein, Eliezer Masliah, Paula Desplats, Seung-Jae Lee, Dong Hwan Ho
Abnormal deposition and intercellular propagation of α-synuclein plays a central role in the pathogenesis of disorders such as Parkinson's Disease (PD) and dementia with Lewy bodies (DLB). Previous studies demonstrated that immunization against α-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff2927b30f8424f654e5365390d4cc3d
https://europepmc.org/articles/PMC3752153/
https://europepmc.org/articles/PMC3752153/
Publikováno v:
Cell Death & Disease
CELL DEATH & DISEASE(6)
CELL DEATH & DISEASE(6)
Lysosomal dysfunction has been implicated both pathologically and genetically in neurodegenerative disorders, such as Alzheimer’s disease and Parkinson’s disease (PD). Lysosomal gene deficiencies cause lysosomal storage disorders, many of which i
Autor:
He Jin Lee, Seung-Jae Lee, Na Young Yang, Sergio Pablo Sardi, Eun Jin Bae, Seokjoong Kim, Cheol Soon Lee
Publikováno v:
Experimental & Molecular Medicine
Lysosomal dysfunction is a common pathological feature of neurodegenerative diseases. GTP-binding protein type A1 (GBA1) encodes β-glucocerebrosidase 1 (GCase 1), a lysosomal hydrolase. Homozygous mutations in GBA1 cause Gaucher disease, the most co
Antibody-Aided Clearance of Extracellular α:-Synuclein Prevents Cell-to-Cell Aggregate Transmission.
Autor:
Eun-Jin Bae, He-Jin Lee, Rockenstein, Edward, Dong-Hwan Ho, Eun-Bi Park, Na-Young Yang, Desplats, Paula, Masliah, Eliezer, Seung-Jae Lee
Publikováno v:
Journal of Neuroscience; 9/26/2012, Vol. 32 Issue 39, p13454-13469, 16p