| scholarly article | Q13442814 |
| P50 | author | Mónica M. Sousa | Q38327590 |
| Pedro Brites | Q40751591 | ||
| Gustavo Maegawa | Q42869922 | ||
| Carla Andreia Teixeira | Q60601186 | ||
| Catarina Oliveira Miranda | Q60601190 | ||
| Telma Emanuela Santos | Q60632899 | ||
| P2093 | author name string | Vera Filipe Sousa | |
| Melani Solomon | |||
| Ana Rita Malheiro | |||
| P2860 | cites work | HDAC6 regulates mitochondrial transport in hippocampal neurons | Q27326879 |
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| In vivo destabilization of dynamic microtubules by HDAC6-mediated deacetylation | Q28585062 | ||
| Molecular cloning and expression of cDNA for murine galactocerebrosidase and mutation analysis of the twitcher mouse, a model of Krabbe's disease | Q28587964 | ||
| Loss of alpha-tubulin polyglutamylation in ROSA22 mice is associated with abnormal targeting of KIF1A and modulated synaptic function | Q28589648 | ||
| Kinesin superfamily motor proteins and intracellular transport | Q29615770 | ||
| Trk activation of the ERK1/2 kinase pathway stimulates intermediate chain phosphorylation and recruits cytoplasmic dynein to signaling endosomes for retrograde axonal transport | Q30419713 | ||
| Microtubule stabilization reduces scarring and causes axon regeneration after spinal cord injury | Q30513561 | ||
| Membrane traffic in sphingolipid storage diseases | Q34156510 | ||
| Dynamics and mechanics of the microtubule plus end | Q34191305 | ||
| NGF causes TrkA to specifically attract microtubules to lipid rafts | Q34230503 | ||
| Post-translational regulation of the microtubule cytoskeleton: mechanisms and functions | Q34232911 | ||
| Lipid rafts in neuronal signaling and function. | Q34750258 | ||
| Psychosine accumulates in membrane microdomains in the brain of krabbe patients, disrupting the raft architecture. | Q34980815 | ||
| Peripheral neuropathy in the Twitcher mouse involves the activation of axonal caspase 3. | Q35335676 | ||
| The twitcher mouse. An alteration of the unmyelinated fibers in the PNS | Q35818487 | ||
| Functions and mechanisms of retrograde neurotrophin signalling | Q36215528 | ||
| Rafting with cholera toxin: endocytosis and trafficking from plasma membrane to ER. | Q36438709 | ||
| The sphingolipid psychosine inhibits fast axonal transport in Krabbe disease by activation of GSK3β and deregulation of molecular motors | Q36928429 | ||
| Characterization and application of a disease-cell model for a neurodegenerative lysosomal disease | Q37624819 | ||
| Axonal damage in leukodystrophies | Q37715458 | ||
| Psychosine induces the dephosphorylation of neurofilaments by deregulation of PP1 and PP2A phosphatases | Q39397868 | ||
| Systemic delivery of bone marrow-derived mesenchymal stromal cells diminishes neuropathology in a mouse model of Krabbe's disease | Q39478232 | ||
| Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington's disease by increasing tubulin acetylation | Q40152899 | ||
| Suppression of galactosylceramidase (GALC) expression in the twitcher mouse model of globoid cell leukodystrophy (GLD) is caused by nonsense-mediated mRNA decay (NMD). | Q40270421 | ||
| Psychosine-induced apoptosis in a mouse oligodendrocyte progenitor cell line is mediated by caspase activation | Q40574853 | ||
| Progressive accumulation of toxic metabolite in a genetic leukodystrophy | Q41595231 | ||
| Axonopathy is a compounding factor in the pathogenesis of Krabbe disease. | Q43118014 | ||
| Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's disease | Q44025845 | ||
| Primary bone marrow mesenchymal stromal cells rescue the axonal phenotype of Twitcher mice | Q45893113 | ||
| Insulin-like growth factor-1 provides protection against psychosine-induced apoptosis in cultured mouse oligodendrocyte progenitor cells using primarily the PI3K/Akt pathway | Q46709267 | ||
| Axonal swellings and degeneration in mice lacking the major proteolipid of myelin | Q48004959 | ||
| Disorganized microtubules underlie the formation of retraction bulbs and the failure of axonal regeneration. | Q50668696 | ||
| The twitcher mouse: accumulation of galactosylsphingosine and pathology of the sciatic nerve. | Q52251298 | ||
| Improved kymography tools and its applications to mitosis. | Q53347612 | ||
| Peripheral neuropathy in globoid cel leucodystrophy (morbus Krabbe). | Q53808447 | ||
| Jamming the endosomal system: lipid rafts and lysosomal storage diseases. | Q55034334 | ||
| Peripheral nerve regeneration | Q68504287 | ||
| Infantile globoid cell leucodystrophy (Krabbe's disease). Some remarks on clinical, biochemical and sural nerve biopsy findings | Q68776905 | ||
| The pathogenesis of globoid cell leucodystrophy in peripheral nerve of the mouse mutant twitcher | Q70485068 | ||
| Hereditary leucodystrophy in the mouse: the new mutant twitcher | Q71327287 | ||
| NGF signaling in sensory neurons: evidence that early endosomes carry NGF retrograde signals | Q73631398 | ||
| Krabbe disease: an ultrastructural study of globoid cells and reactive astrocytes at the brain and optic nerves | Q74574531 | ||
| Fibrin inhibits peripheral nerve remyelination by regulating Schwann cell differentiation | Q77800094 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P304 | page(s) | 92-103 | |
| P577 | publication date | 2014-03-06 | |
| P1433 | published in | Neurobiology of Disease | Q15716606 |
| P1476 | title | Early axonal loss accompanied by impaired endocytosis, abnormal axonal transport, and decreased microtubule stability occur in the model of Krabbe's disease | |
| P478 | volume | 66 |
| Q41829569 | A Comparative Study on the Alterations of Endocytic Pathways in Multiple Lysosomal Storage Disorders |
| Q92144962 | Alterations in Cellular Processes Involving Vesicular Trafficking and Implications in Drug Delivery |
| Q38957250 | Axonal pathology in Krabbe's disease: The cytoskeleton as an emerging therapeutic target |
| Q100958519 | Brainstem development requires galactosylceramidase and is critical for pathogenesis in a model of Krabbe disease |
| Q30657387 | Combined gene/cell therapies provide long-term and pervasive rescue of multiple pathological symptoms in a murine model of globoid cell leukodystrophy |
| Q37265504 | How membrane dysfunction influences neuronal survival pathways in sphingolipid storage disorders |
| Q55194774 | Human iPSC-based models highlight defective glial and neuronal differentiation from neural progenitor cells in metachromatic leukodystrophy. |
| Q38805611 | Inherited and acquired disorders of myelin: The underlying myelin pathology |
| Q91622067 | Inhibition of the IGF-1-PI3K-Akt-mTORC2 pathway in lipid rafts increases neuronal vulnerability in a genetic lysosomal glycosphingolipidosis |
| Q58479932 | Is Parkinson's disease a lysosomal disorder? |
| Q50056656 | Long-Term Improvement of Neurological Signs and Metabolic Dysfunction in a Mouse Model of Krabbe's Disease after Global Gene Therapy. |
| Q28555118 | Lysosomal Re-acidification Prevents Lysosphingolipid-Induced Lysosomal Impairment and Cellular Toxicity |
| Q38684097 | Lysosomal enzyme replacement therapies: Historical development, clinical outcomes, and future perspectives |
| Q38957237 | Lysosphingolipids and sphingolipidoses: Psychosine in Krabbe's disease |
| Q35020269 | Mechanism of neuromuscular dysfunction in Krabbe disease. |
| Q48237077 | Midbrain morphology reflects extent of brain damage in Krabbe disease. |
| Q26797407 | Myelin damage and repair in pathologic CNS: challenges and prospects |
| Q89920152 | Neuropathophysiology of Lysosomal Storage Diseases: Synaptic Dysfunction as a Starting Point for Disease Progression |
| Q37688803 | Patient fibroblasts-derived induced neurons demonstrate autonomous neuronal defects in adult-onset Krabbe disease |
| Q38957277 | Perspective on innovative therapies for globoid cell leukodystrophy. |
| Q38938894 | Role of extracellular calcium and mitochondrial oxygen species in psychosine-induced oligodendrocyte cell death |
| Q38559219 | Synaptic failure: The achilles tendon of sphingolipidoses |
| Q38957263 | Treatment for Krabbe's disease: Finding the combination. |
| Q38820041 | Ultrastructural Characterization of the Lower Motor System in a Mouse Model of Krabbe Disease. |
| Q92124409 | δ-Tocopherol Effect on Endocytosis and Its Combination with Enzyme Replacement Therapy for Lysosomal Disorders: A New Type of Drug Interaction? |
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