| P2093 | author name string | Robert E Schmidt | |
| | Richard W Gross | |
| | John Turk | |
| | Mary Wohltmann | |
| | David F Wozniak | |
| | Paul T Kotzbauer | |
| | David J Mancuso | |
| | Ibrahim Malik | |
| | Laura Montier | |
| P2860 | cites work | Misfolding diverts CFTR from recycling to degradation: quality control at early endosomes | Q24676764 |
| | Differential regulation of EGF receptor internalization and degradation by multiubiquitination within the kinase domain | Q28119149 |
| | Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis | Q28131672 |
| | Altered neuronal mitochondrial coenzyme A synthesis in neurodegeneration with brain iron accumulation caused by abnormal processing, stability, and catalytic activity of mutant pantothenate kinase 2 | Q28303208 |
| | Genetic and age related models of neurodegeneration in mice: dystrophic axons | Q28507600 |
| | Neuropathology of gracile axonal dystrophy (GAD) mouse. An animal model of central distal axonopathy in primary sensory neurons | Q28594561 |
| | Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice | Q30764264 |
| | Highly selective hydrolysis of fatty acyl-CoAs by calcium-independent phospholipase A2beta. Enzyme autoacylation and acyl-CoA-mediated reversal of calmodulin inhibition of phospholipase A2 activity | Q33238930 |
| | Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course | Q34019790 |
| | PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron | Q34568479 |
| | Neuropathology and pathogenesis of diabetic autonomic neuropathy | Q34800404 |
| | PLA2G6 mutation underlies infantile neuroaxonal dystrophy | Q35221441 |
| | Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathology | Q35745646 |
| | Neuroaxonal dystrophy in aging human sympathetic ganglia | Q35811753 |
| | Neurodegenerative diseases: a decade of discoveries paves the way for therapeutic breakthroughs | Q35906130 |
| | Insulin secretory responses and phospholipid composition of pancreatic islets from mice that do not express Group VIA phospholipase A2 and effects of metabolic stress on glucose homeostasis. | Q36097167 |
| | Spontaneous murine neuroaxonal dystrophy: a model of infantile neuroaxonal dystrophy | Q36177182 |
| | Male mice that do not express group VIA phospholipase A2 produce spermatozoa with impaired motility and have greatly reduced fertility. | Q37070443 |
| | Lysosomal targeting of E-cadherin: a unique mechanism for the down-regulation of cell-cell adhesion during epithelial to mesenchymal transitions | Q40480362 |
| | Amyloid beta precursor protein and ubiquitin epitopes in human and experimental dystrophic axons. Ultrastructural localization | Q42050045 |
| | Widespread occurrence of alpha-synuclein/NACP-immunoreactive neuronal inclusions in juvenile and adult-onset Hallervorden-Spatz disease with Lewy bodies | Q42479971 |
| | Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and lewy body pathology | Q42483324 |
| | Infantile neuroaxonal dystrophy (Seitelberger's disease). A light and ultrastructural study | Q43572126 |
| | Terminal axon pathology in infantile neuroaxonal dystrophy | Q44734791 |
| | Apoptotic neurodegeneration induced by ethanol in neonatal mice is associated with profound learning/memory deficits in juveniles followed by progressive functional recovery in adults | Q45168372 |
| | Fibrillization of alpha-synuclein and tau in familial Parkinson's disease caused by the A53T alpha-synuclein mutation | Q47602087 |
| | An analysis of the ultrastructural findings in infantile neuroaxonal dystrophy (Seitelberger's disease). | Q47852922 |
| | Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria | Q48221200 |
| | Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases | Q48221796 |
| | Histological and ultrastructural features of dystrophic isocortical axons in infantile neuroaxonal dystrophy (Seitelberger's disease). | Q48550671 |
| | Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein | Q48581887 |
| | Infantile neuroaxonal dystrophy. Histological and electron microscopical study of two cases | Q48599352 |
| | Cerebellar synaptic defects and abnormal motor behavior in mice lacking alpha- and beta-dystrobrevin. | Q48616988 |
| | Neuroaxonal dystrophy in young adults: a clinicopathological study of two unrelated cases | Q48957543 |
| | Alpha-synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies | Q57188685 |
| | Alpha-synuclein immunoreactivity is present in axonal swellings in neuroaxonal dystrophy and acute traumatic brain injury | Q64816474 |
| | Infantile neuroaxonal dystrophy | Q66971406 |
| | Infantile neuroaxonal dystrophy. Early form with preferential cerebellar involvement | Q72183166 |
| | Involvement of group VI Ca2+-independent phospholipase A2 in protein kinase C-dependent arachidonic acid liberation in zymosan-stimulated macrophage-like P388D1 cells | Q77955228 |
| | Both proteasomes and lysosomes degrade the activated erythropoietin receptor | Q80546895 |
| | A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1 | Q81696532 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | protein ubiquitination | Q3547638 |
| | Infantile neuroaxonal dystrophy | Q6029060 |
| P304 | page(s) | 406-416 | |
| P577 | publication date | 2008-01-17 | |
| P1433 | published in | The American Journal of Pathology | Q4744259 |
| P1476 | title | Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations | |
| P478 | volume | 172 | |