| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S0161-813X(02)00062-1 |
| P698 | PubMed publication ID | 12428732 |
| P2093 | author name string | Jennifer L Mazzola | |
| Michael A Sirover | |||
| P2860 | cites work | Atrophin-1, the dentato-rubral and pallido-luysian atrophy gene product, interacts with ETO/MTG8 in the nuclear matrix and represses transcription | Q24290194 |
| Glyceraldehyde-3-phosphate dehydrogenase is phosphorylated by protein kinase Ciota /lambda and plays a role in microtubule dynamics in the early secretory pathway | Q24291938 | ||
| Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons | Q24317574 | ||
| Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain | Q24324461 | ||
| alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies | Q24653247 | ||
| Alpha-synuclein in Lewy bodies | Q27860680 | ||
| Alpha-synuclein and neurodegenerative diseases | Q28204386 | ||
| Cell biology of the amyloid beta-protein precursor and the mechanism of Alzheimer's disease | Q28236160 | ||
| Glyceraldehyde-3-phosphate dehydrogenase, the putative target of the antiapoptotic compounds CGP 3466 and R-(-)-deprenyl | Q28263664 | ||
| Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase | Q28293728 | ||
| Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form | Q28509836 | ||
| The intracellular domain of the beta-amyloid precursor protein is stabilized by Fe65 and translocates to the nucleus in a notch-like manner | Q28510317 | ||
| Parkin is associated with cellular vesicles | Q28578692 | ||
| Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organelles | Q28589989 | ||
| Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice | Q29615357 | ||
| New insights into an old protein: the functional diversity of mammalian glyceraldehyde-3-phosphate dehydrogenase. | Q30322264 | ||
| Reduction of glyceraldehyde-3-phosphate dehydrogenase activity in Alzheimer's disease and in Huntington's disease fibroblasts | Q32034809 | ||
| Moonlighting proteins. | Q33543960 | ||
| Genetics of Parkinsonism: a review | Q34293891 | ||
| Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat | Q34662620 | ||
| Glyceraldehyde-3-phosphate dehydrogenase: nuclear translocation participates in neuronal and nonneuronal cell death | Q36605673 | ||
| Subcellular localization of the Huntington's disease gene product in cell lines by immunofluorescence and biochemical subcellular fractionation | Q36823776 | ||
| Transglutaminase-catalyzed inactivation of glyceraldehyde 3-phosphate dehydrogenase and alpha-ketoglutarate dehydrogenase complex by polyglutamine domains of pathological length | Q36826440 | ||
| Glyceraldehyde-3-phosphate dehydrogenase antisense oligodeoxynucleotides protect against cytosine arabinonucleoside-induced apoptosis in cultured cerebellar neurons | Q37368739 | ||
| Genetics and molecular biology of Huntington's disease | Q40399297 | ||
| Transfection-enforced Bcl-2 overexpression and an anti-Parkinson drug, rasagiline, prevent nuclear accumulation of glyceraldehyde-3-phosphate dehydrogenase induced by an endogenous dopaminergic neurotoxin, N-methyl(R)salsolinol | Q40783945 | ||
| alpha-Synuclein forms a complex with transcription factor Elk-1. | Q40816103 | ||
| Glyceraldehyde-3-phosphate dehydrogenase is required for vesicular transport in the early secretory pathway | Q40849095 | ||
| In vitro evidence for both the nucleus and cytoplasm as subcellular sites of pathogenesis in Huntington's disease. | Q40981007 | ||
| The influence of huntingtin protein size on nuclear localization and cellular toxicity. | Q41035353 | ||
| Trinucleotide instability: a repeating theme in human inherited disorders | Q41036331 | ||
| Huntington disease: new insights into the relationship between CAG expansion and disease | Q41170305 | ||
| Increased beta-amyloid release and levels of amyloid precursor protein (APP) in fibroblast cell lines from family members with the Swedish Alzheimer's disease APP670/671 mutation. | Q41429343 | ||
| Aberrant proteolysis of the beta-amyloid precursor protein in familial Alzheimer's disease lymphoblastoid cells | Q41524470 | ||
| Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia. | Q42438521 | ||
| Amyloid precursor protein metabolism in fibroblasts from individuals with one, two or three copies of the amyloid precursor protein (APP) gene | Q42993144 | ||
| The amyloid precursor protein (APP)-cytoplasmic fragment generated by gamma-secretase is rapidly degraded but distributes partially in a nuclear fraction of neurones in culture | Q43735231 | ||
| Alteration of nuclear glyceraldehyde-3-phosphate dehydrogenase structure in Huntington's disease fibroblasts | Q43991317 | ||
| Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH. | Q45291767 | ||
| Glyceraldehyde 3-phosphate dehydrogenase abnormality in metabolically stressed Huntington disease fibroblasts. | Q45296630 | ||
| Brain glyceraldehyde-3-phosphate dehydrogenase activity in human trinucleotide repeat disorders | Q45296636 | ||
| Biochemical abnormalities and excitotoxicity in Huntington's disease brain. | Q45297145 | ||
| Fibroblast models of neurological disorders: fluorescence measurement studies | Q47888489 | ||
| Parieto-occipital glucose hypometabolism in Parkinson's disease with autonomic failure | Q48185492 | ||
| Nuclear translocation of glyceraldehyde-3-phosphate dehydrogenase isoforms during neuronal apoptosis | Q48275909 | ||
| Motor correlates of occipital glucose hypometabolism in Parkinson's disease without dementia | Q48279827 | ||
| Increased glyceraldehyde 3-phosphate dehydrogenase levels in the brain of patients with Down's syndrome | Q48279897 | ||
| Rat brain glyceraldehyde-3-phosphate dehydrogenase interacts with the recombinant cytoplasmic domain of Alzheimer's beta-amyloid precursor protein | Q48291777 | ||
| Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice | Q48373570 | ||
| Nuclear localization of overexpressed glyceraldehyde-3-phosphate dehydrogenase in cultured cerebellar neurons undergoing apoptosis | Q48477126 | ||
| Subcellular distribution of glyceraldehyde-3-phosphate dehydrogenase in cerebellar granule cells undergoing cytosine arabinoside-induced apoptosis | Q48544021 | ||
| Selective hypometabolism in the inferior frontal lobe in depressed patients with Parkinson's disease | Q48939047 | ||
| Parkin is associated with actin filaments in neuronal and nonneural cells | Q58856664 | ||
| Fluorodopa uptake and glucose metabolism in early stages of corticobasal degeneration | Q59858824 | ||
| Increased caspase 3 and Bax immunoreactivity accompany nuclear GAPDH translocation and neuronal apoptosis in Parkinson's disease | Q64767727 | ||
| Glyceraldehyde-3-phosphate dehydrogenase is over-expressed during apoptotic death of neuronal cultures and is recognized by a monoclonal antibody against amyloid plaques from Alzheimer's brain | Q71041832 | ||
| Protein kinase C and amyloid precursor protein processing in skin fibroblasts from sporadic and familial Alzheimer's disease cases | Q74665994 | ||
| P433 | issue | 4-5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | neurodegeneration | Q1755122 |
| P304 | page(s) | 603-9 | |
| P577 | publication date | 2002-10-01 | |
| P1433 | published in | NeuroToxicology | Q15098069 |
| P1476 | title | Alteration of intracellular structure and function of glyceraldehyde-3-phosphate dehydrogenase: a common phenotype of neurodegenerative disorders? | |
| P478 | volume | 23 |
| Q40616428 | A Novel CRM1-mediated Nuclear Export Signal Governs Nuclear Accumulation of Glyceraldehyde-3-phosphate Dehydrogenase following Genotoxic Stress |
| Q90481282 | A dedicated glyceraldehyde-3-phosphate dehydrogenase is involved in the biosynthesis of volatile sesquiterpenes in Trichoderma virens-evidence for the role of a fungal GAPDH in secondary metabolism |
| Q28507691 | Age-dependent motor deficits and dopaminergic dysfunction in DJ-1 null mice |
| Q44546799 | Ascorbate-induced oxidation of glyceraldehyde-3-phosphate dehydrogenase |
| Q34627867 | Differencial proteome of clear-cell renal cell carcinoma (ccRCC) tissues |
| Q46516306 | Downregulation of myelination, energy, and translational genes in Menkes disease brain |
| Q40487130 | GAPDH binds Akt to facilitate cargo transport in the early secretory pathway |
| Q28271053 | GAPDH, a novel regulator of the pro-apoptotic mitochondrial membrane permeabilization |
| Q43223713 | Glyceraldehyde-3-phosphate dehydrogenase tetramer dissociation and amyloid fibril formation induced by negatively charged membranes. |
| Q36159463 | Impaired GAPDH-induced mitophagy contributes to the pathology of Huntington's disease |
| Q47919912 | Inactivation of glyceraldehyde-3-phosphate dehydrogenase by the dopamine metabolite, 3,4-dihydroxyphenylacetaldehyde |
| Q36001244 | Inhibition of GAPDH activity by poly(ADP-ribose) polymerase activates three major pathways of hyperglycemic damage in endothelial cells |
| Q28237811 | Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's disease |
| Q36525167 | Liquid chromatography with tandem mass spectrometry-based proteomic discovery in aging and Alzheimer's disease |
| Q36110567 | Nucleocytoplasmic transport in apoptosis |
| Q44533951 | Oxidation of glyceraldehyde-3-phosphate dehydrogenase enhances its binding to nucleic acids |
| Q38775811 | Protein DJ-1 and its anti-oxidative stress function play an important role in renal cell mediated response to profibrotic agents. |
| Q41786059 | Protein reactivity of 3,4-dihydroxyphenylacetaldehyde, a toxic dopamine metabolite, is dependent on both the aldehyde and the catechol |
| Q37893585 | Proteins with neomorphic moonlighting functions in disease. |
| Q33336630 | Proteomic analysis of differential proteins related to the neuropathic pain and neuroprotection in the dorsal root ganglion following its chronic compression in rats |
| Q33564752 | Proteomic analysis of the Arabidopsis nucleolus suggests novel nucleolar functions |
| Q48738688 | Reduction of GAPDH in lenses of Parkinson's disease patients: A possible new biomarker |
| Q33315270 | Removal of high-abundance proteins for nuclear subproteome studies in rice (Oryza sativa) endosperm |
| Q27025760 | Subcellular dynamics of multifunctional protein regulation: mechanisms of GAPDH intracellular translocation |
| Q28291106 | The diverse functions of GAPDH: views from different subcellular compartments |
| Q37801584 | The nucleolus and viral infection. |
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