[HTML][HTML] Gangliosides in the brain: physiology, pathophysiology and therapeutic applications
Gangliosides are glycosphingolipids highly abundant in the nervous system, and carry most
of the sialic acid residues in the brain. Gangliosides are enriched in cell membrane …
of the sialic acid residues in the brain. Gangliosides are enriched in cell membrane …
[HTML][HTML] Emerging phagocytosis checkpoints in cancer immunotherapy
Cancer immunotherapy, mainly including immune checkpoints-targeted therapy and the
adoptive transfer of engineered immune cells, has revolutionized the oncology landscape as …
adoptive transfer of engineered immune cells, has revolutionized the oncology landscape as …
Sialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regeneration
RL Schnaar, R Gerardy-Schahn… - Physiological …, 2014 - journals.physiology.org
Every cell in nature carries a rich surface coat of glycans, its glycocalyx, which constitutes
the cell's interface with its environment. In eukaryotes, the glycocalyx is composed of …
the cell's interface with its environment. In eukaryotes, the glycocalyx is composed of …
N omenclature of genetic movement disorders: R ecommendations of the international P arkinson and movement disorder society task force
C Marras, A Lang, BP van de Warrenburg… - Movement …, 2016 - Wiley Online Library
The system of assigning locus symbols to specify chromosomal regions that are associated
with a familial disorder has a number of problems when used as a reference list of …
with a familial disorder has a number of problems when used as a reference list of …
[HTML][HTML] Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms
TL Giudice, F Lombardi, FM Santorelli, T Kawarai… - Experimental …, 2014 - Elsevier
Hereditary spastic paraplegia (HSP) is a group of clinically and genetically heterogeneous
neurological disorders characterized by pathophysiologic hallmark of length-dependent …
neurological disorders characterized by pathophysiologic hallmark of length-dependent …
[HTML][HTML] Siglec ligands
A Gonzalez-Gil, RL Schnaar - Cells, 2021 - mdpi.com
A dense and diverse array of glycans on glycoproteins and glycolipids decorate all cell
surfaces. In vertebrates, many of these carry sialic acid, in a variety of linkages and glycan …
surfaces. In vertebrates, many of these carry sialic acid, in a variety of linkages and glycan …
Hereditary spastic paraplegia: clinical and genetic hallmarks
PVS de Souza, WBV de Rezende Pinto… - The Cerebellum, 2017 - Springer
Hereditary spastic paraplegia comprises a wide and heterogeneous group of inherited
neurodegenerative and neurodevelopmental disorders resulting from primary retrograde …
neurodegenerative and neurodevelopmental disorders resulting from primary retrograde …
Sphingolipid lysosomal storage disorders
FM Platt - Nature, 2014 - nature.com
Lysosomal storage diseases are inborn errors of metabolism, the hallmark of which is the
accumulation, or storage, of macromolecules in the late endocytic system. They are …
accumulation, or storage, of macromolecules in the late endocytic system. They are …
[HTML][HTML] Insights into clinical, genetic, and pathological aspects of hereditary spastic paraplegias: a comprehensive overview
LEO Elsayed, IZ Eltazi, AE Ahmed… - Frontiers in Molecular …, 2021 - frontiersin.org
Hereditary spastic paraplegias (HSP) are a heterogeneous group of motor
neurodegenerative disorders that have the core clinical presentation of pyramidal syndrome …
neurodegenerative disorders that have the core clinical presentation of pyramidal syndrome …
Neurological aspects of human glycosylation disorders
HH Freeze, EA Eklund, BG Ng… - Annual review of …, 2015 - annualreviews.org
This review presents principles of glycosylation, describes the relevant glycosylation
pathways and their related disorders, and highlights some of the neurological aspects and …
pathways and their related disorders, and highlights some of the neurological aspects and …