S100B, S100 calcium binding protein B, 6285

N. diseases: 599; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.070 Biomarker disease BEFREE This review addresses this novel scenario, presenting data indicating that S100B levels and/or distribution in the nervous tissue of patients and/or experimental models of different neural disorders, for which the protein is used as a biomarker, are directly related to the progress of the disease: acute brain injury (ischemic/hemorrhagic stroke, traumatic injury), neurodegenerative diseases (Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, multiple sclerosis), congenital/perinatal disorders (Down syndrome, spinocerebellar ataxia-1), psychiatric disorders (schizophrenia, mood disorders), inflammatory bowel disease. 30144068 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.070 Biomarker disease BEFREE Preclinical and clinical evidences have demonstrated that astroglial-derived S100B protein is a key element in neuroinflammation underlying the pathogenesis of Parkinson's disease (PD), so much as that S100B inhibitors have been proposed as promising candidates for PD targeted therapy. 30529726 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.070 Biomarker disease BEFREE The S100B SNPs tested were not associated with the risk of PD. 29529989 2018
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.070 Biomarker disease BEFREE Naturally occurring autoantibodies (NAbs) against a number of potentially disease-associated cellular proteins, including Amyloid-beta1-42 (Abeta1-42), Alpha-synuclein (Asyn), myelin basic protein (MBP), myelin oligodendrocyte glycoprotein (MOG), and S100 calcium binding protein B (S100B) have been suggested to be associated with neurodegenerative disorders, in particular Alzheimer's (AD) and Parkinson's disease (PD). 24586351 2014
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.070 GeneticVariation disease BEFREE Our results suggest that mutations in the coding region or intron/exon boundaries of the S100B gene play little or no role in the development of PD in Chinese population. 24076007 2013
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.070 Biomarker disease BEFREE Our results demonstrate a role of S100B in the pathophysiology of Parkinson's disease. 23169921 2012
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.070 Biomarker disease BEFREE We undertook this study to establish the brain-specific S100B gene transgenic mice and investigate the role of S100B in the development of PD. 21376255 2011