Results 11 to 20 of about 56,805 (280)

Anti-ganglioside M1 autoantibodies in Egyptian children with autism: a cross-sectional comparative study

open access: yesMiddle East Current Psychiatry, 2022
Background Autism may be one of the pediatric autoimmune neuropsychiatric disorders, and several studies investigated the frequency of serum anti-ganglioside M1 autoantibodies in children with autism, as possible indicators of autoimmunity to the brain ...
Reham Mohammad Raafat Hamed   +3 more
doaj   +1 more source

Simultaneous measurements of auto-immune and infectious disease specific antibodies using a high throughput multiplexing tool. [PDF]

open access: yesPLoS ONE, 2012
Considering importance of ganglioside antibodies as biomarkers in various immune-mediated neuropathies and neurological disorders, we developed a high throughput multiplexing tool for the assessment of gangliosides-specific antibodies based on Biolpex ...
Atul Asati   +2 more
doaj   +1 more source

GM1 Ganglioside Is A Key Factor in Maintaining the Mammalian Neuronal Functions Avoiding Neurodegeneration

open access: yesInternational Journal of Molecular Sciences, 2020
Many species of ganglioside GM1, differing for the sialic acid and ceramide content, have been characterized and their physico-chemical properties have been studied in detail since 1963.
E. Chiricozzi   +5 more
semanticscholar   +1 more source

Mechanism of Secondary Ganglioside and Lipid Accumulation in Lysosomal Disease

open access: yesInternational Journal of Molecular Sciences, 2020
Gangliosidoses are caused by monogenic defects of a specific hydrolase or an ancillary sphingolipid activator protein essential for a specific step in the catabolism of gangliosides.
Bernadette Breiden, K. Sandhoff
semanticscholar   +1 more source

Antibody recognition of cancer-related gangliosides and their mimics investigated using in silico site mapping. [PDF]

open access: yesPLoS ONE, 2012
Modified gangliosides may be overexpressed in certain types of cancer, thus, they are considered a valuable target in cancer immunotherapy. Structural knowledge of their interaction with antibodies is currently limited, due to the large size and high ...
Mark Agostino   +2 more
doaj   +1 more source

A Variant Guillain-Barré Syndrome with Anti-Ganglioside Complex Antibody [PDF]

open access: yesJournal of Neurocritical Care, 2018
Background Recently, anti-ganglioside complex (GSC) antibodies were discovered among the various subtypes of Guillain-Barré syndrome. GSC is the novel glycoepitopes formed by two individual ganglioside molecules.
So-Young Huh   +6 more
doaj   +1 more source

Deficiency of the frontotemporal dementia gene GRN results in gangliosidosis

open access: yesNature Communications, 2022
Progranulin-deficieny results in gangliosidosis due to reduced lysosomal lipids (BMP) required for ganglioside degradation. Lysosomal ganglioside accumulation may contribute to neuroinflammation and neurodegeneration susceptibility observed in FTD.
Sebastian Boland   +18 more
doaj   +1 more source

Neuropathophysiological potential of Guillain-Barré syndrome anti-ganglioside-complex antibodies at mouse motor nerve terminals [PDF]

open access: yes, 2011
Objectives:  Anti-ganglioside antibodies are present in approximately half of Guillain–Barré syndrome (GBS) patients. Recently, it has been shown that a considerable proportion of these patients has serum antibodies against antigenic epitopes formed by a
Susumu Kusunoki   +32 more
core   +1 more source

Structural basis of tetanus toxin neutralization by native human monoclonal antibodies

open access: yesCell Reports, 2021
Summary: Four potent native human monoclonal antibodies (mAbs) targeting distinct epitopes on tetanus toxin (TeNT) are isolated with neutralization potency ranging from approximately 17 mg to 6 mg each that are equivalent to 250 IU of human anti-TeNT ...
Yueming Wang   +18 more
doaj   +1 more source

Reduced sphingolipid hydrolase activities, substrate accumulation and ganglioside decline in Parkinson’s disease

open access: yesMolecular Neurodegeneration, 2019
Haploinsufficiency in the Gaucher disease GBA gene, which encodes the lysosomal glucocerebrosidase GBA, and ageing represent major risk factors for developing Parkinson’s disease (PD).
Mylene Huebecker   +6 more
semanticscholar   +1 more source

Home - About - Disclaimer - Privacy