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

Nobuhiro Yuki, T. Taki, Fuyuhiko Inagaki, +5

The Journal of Experimental Medicine

ImmunologyGlycobiologyPathologyMedical MicrobiologyNeurobiology Of Disease +16

Mitochondrial angiopathy in cerebral blood vessels of mitochondrial eneephalomyopathy

Eisaku Ohama, S. Ohara, Fusahiro Ikuta, +3

Acta Neuropathologica

Mitochondrial MyopathyMitochondrial FunctionMitochondrial AngiopathyBrain InjuryNeuroscience +4

Molecular cloning of human growth inhibitory factor cDNA and its down-regulation in Alzheimer's disease.

Shoji Tsuji, Hirofumi Kobayashi, Yoshihito Uchida, +2

The EMBO Journal

Neurodegenerative DiseasesDevelopmental BiologyAlzheimer's DiseaseHuman GrowthDegenerative Pathology +6

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles.

Makoto Yoneda, T. Miyatake, Giuseppe Attardi

Molecular and Cellular Biology

DnaGeneticsMolecular BiologyMolecular GeneticsGenomics +15

An immunologic abnormality common to Bickerstaff's brain stem encephalitis and Fisher's syndrome

Nobuhiro Yuki, Shuzo Sato, Shoji Tsuji, +2

Journal of the Neurological Sciences

MedicineImmunologyPathologyBrain Stem EncephalitisImmunologic Abnormality +5

Molecular mimicry between GQ_1b ganglioside and lipopolysaccharides of <i>Campylobacter jejuni</i> isolated from patients with Fisher's syndrome

Nobuhiro Yuki, T. Taki, Masaki Takahashi, +5

Annals of Neurology

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibers.

Makoto Yoneda, Yoshinori Tanno, Satoshi Horai, +3

PubMed

GeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationMyoclonus Epilepsy +14

Penner's serotype 4 of Campylobacter jejuni has a lipopolysaccharide that bears a GM1 ganglioside epitope as well as one that bears a GD1 a epitope

Nobuhiro Yuki, T. Taki, Masaki Takahashi, +4

Infection and Immunity

GlycobiologyPathologyPolysaccharideLps FractionMedical Microbiology +15

A novel exon mutation in the human beta-hexosaminidase beta subunit gene affects 3' splice site selection.

Nobuaki Wakamatsu, Hirofumi Kobayashi, T. Miyatake, +1

Journal of Biological Chemistry

Splice Site SelectionSystems BiologyGenetic DisorderGeneticsGene Structure +11

Clinical comparison of Alzheimer's disease in pedigrees with the codon 717 Val→Ile mutation in the amyloid precursor protein gene

Michael Mullan, Shoji Tsuji, T. Miki, +20

Neurobiology of Aging

Neurodegenerative DiseasesCodon 717Alzheimer's DiseaseVal→ile MutationGenetics +8