Carbohydrate mimicry between human ganglioside GM1 and Campylobacter jejuni lipooligosaccharide causes Guillain-Barre syndrome. - Test2 - elhamkhani - TriplyDB

Carbohydrate mimicry between human ganglioside GM1 and Campylobacter jejuni lipooligosaccharide causes Guillain-Barre syndrome.

Carbohydrate mimicry between human ganglioside GM1 and Campylobacter jejuni lipooligosaccharide causes Guillain-Barre syndrome.

http://www.wikidata.org/entity/Q30827235

about

Fisher syndrome: clinical features, immunopathogenesis and management The role of infections in autoimmune disease Guillain–Barré Syndrome—A Classical Autoimmune Disease Triggered by Infection or Vaccination Prospects for vaccine prevention of meningococcal infection Identification of Cd101 as a susceptibility gene for Novosphingobium aromaticivorans-induced liver autoimmunity Autoimmune disease triggered by infection with alphaproteobacteria The role of the gut microbiota in the pathogenesis of antiphospholipid syndrome Sialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regeneration Molecular mimicry in pauci-immune focal necrotizing glomerulonephritis Structural and Kinetic Analysis of Substrate Binding to the Sialyltransferase Cst-II from Campylobacter jejuni Microbe Hunting Erythropoietin enhances nerve repair in anti-ganglioside antibody-mediated models of immune neuropathy [Guillain-Barré syndrome after exposure to influenza].Comparative genomic analysis of Campylobacter jejuni associated with Guillain-Barré and Miller Fisher syndromes: neuropathogenic and enteritis-associated isolates can share high levels of genomic similarity.Prominent plasmacytosis following intravenous immunoglobulin correlates with clinical improvement in Guillain-Barré syndrome.Helicobacter pylori eradication shifts monocyte Fcgamma receptor balance toward inhibitory FcgammaRIIB in immune thrombocytopenic purpura patients.AI-2 does not function as a quorum sensing molecule in Campylobacter jejuni during exponential growth in vitro.Host factors determine anti-GM1 response following oral challenge of chickens with Guillain-Barré syndrome derived Campylobacter jejuni strain GB11.Epidemiology of Campylobacter jejuni isolated from patients with Guillain-Barré and Fisher syndromes in Japan.Uncovering cryptic glycan markers in multiple sclerosis (MS) and experimental autoimmune encephalomyelitis (EAE).Temperature-dependent phenotypic variation of Campylobacter jejuni lipooligosaccharides Novel immune response to gluten in individuals with schizophrenia Mechanisms underlying autoimmune synaptic encephalitis leading to disorders of memory, behavior and cognition: insights from molecular, cellular and synaptic studies An update on pathobiologic roles of anti-glycan antibodies in Guillain-Barré syndrome.Sialylation of Campylobacter jejuni lipo-oligosaccharides: impact on phagocytosis and cytokine production in mice.Role of sphingolipids in microbial pathogenesis Structural heterogeneity of terminal glycans in Campylobacter jejuni lipooligosaccharides.Exposure to mimivirus collagen promotes arthritis.Guillain-barré syndrome animal model: the first proof of molecular mimicry in human autoimmune disorder.Development of a novel therapy for Lipo-oligosaccharide-induced experimental neuritis: use of peptide glycomimics Bioengineered bugs expressing oligosaccharide receptor mimics: toxin-binding probiotics for treatment and prevention of enteric infections Flagellin-independent regulation of chemokine host defense in Campylobacter jejuni-infected intestinal epithelium.Improved serological diagnosis stresses the major role of Campylobacter jejuni in triggering Guillain-Barré syndrome.Are dysregulated inflammatory responses to commensal bacteria involved in the pathogenesis of hepatobiliary-pancreatic autoimmune disease? An analysis using mice models of primary biliary cirrhosis and autoimmune pancreatitis.Ganglioside molecular mimicry and its pathological roles in Guillain-Barré syndrome and related diseases Complex of GM1- and GD1a-like lipo-oligosaccharide mimics GM1b, inducing anti-GM1b antibodies.Anti-Ganglioside Antibodies Induce Nodal and Axonal Injury via Fcγ Receptor-Mediated Inflammation.Campylobacter jejuni induces colitis through activation of mammalian target of rapamycin signaling.Environmental pathways to autoimmune diseases: the cases of primary biliary cirrhosis and multiple sclerosis.Dysfunction of nodes of Ranvier: a mechanism for anti-ganglioside antibody-mediated neuropathies.

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Carbohydrate mimicry between human ganglioside GM1 and Campylobacter jejuni lipooligosaccharide causes Guillain-Barre syndrome.

http://www.wikidata.org/entity/Q30827235

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2004 nî lūn-bûn

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2004年の論文

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Carbohydrate mimicry between h ...... auses Guillain-Barre syndrome.

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Carbohydrate mimicry between h ...... auses Guillain-Barre syndrome.

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Carbohydrate mimicry between h ...... auses Guillain-Barre syndrome.

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Carbohydrate mimicry between h ...... auses Guillain-Barre syndrome.

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Carbohydrate mimicry between h ...... auses Guillain-Barre syndrome.

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Proceedings of the National Academy of Sciences of the United States of America

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Carbohydrate mimicry between h ...... auses Guillain-Barre syndrome.

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Keiichiro Susuki

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Koichi Furukawa

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Koichi Hirata

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Kyoji Taguchi

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Masaaki Odaka

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Michiaki Koga

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Mitsunori Yamada

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Tadashi Miyatake

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Tetsuji Kobata

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Yukihiro Nishimoto

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P2860

Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

Mice with disrupted GM2/GD2 synthase gene lack complex gangliosides but exhibit only subtle defects in their nervous system

Autoimmune disease: why and where it occurs.

Infectious origins of, and molecular mimicry in, Guillain-Barré and Fisher syndromes.

Acute motor axonal neuropathy: a frequent cause of acute flaccid paralysis in China.

A bacterium lipopolysaccharide that elicits Guillain-Barré syndrome has a GM1 ganglioside-like structure.

A full complement of receptors in immune complex diseases.

Molecular mimicry: can epitope mimicry induce autoimmune disease?

Molecular mimicry between GQ1b ganglioside and lipopolysaccharides of Campylobacter jejuni isolated from patients with Fisher's syndrome.

Early nodal changes in the acute motor axonal neuropathy pattern of the Guillain-Barré syndrome.

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Guillain–Barré Syndrome

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