Pages that link to "Q28511439"
Jump to navigation
Jump to search
The following pages link to A mutant neurofilament subunit causes massive, selective motor neuron death: implications for the pathogenesis of human motor neuron disease (Q28511439):
Displaying 50 items.
- Neurofilament, light polypeptide (Q21987272) (← links)
- Mutations in the neurofilament light gene linked to Charcot-Marie-Tooth disease cause defects in transport (Q24300855) (← links)
- Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis (Q24306886) (← links)
- A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene (Q24538715) (← links)
- Dysfunctions of neuronal and glial intermediate filaments in disease (Q24657653) (← links)
- Role of Intermediate Filaments in Vesicular Traffic (Q26749357) (← links)
- From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS (Q28206361) (← links)
- Stable tubule only polypeptides (STOP) proteins co-aggregate with spheroid neurofilaments in amyotrophic lateral sclerosis (Q28235829) (← links)
- The complex molecular biology of amyotrophic lateral sclerosis (ALS) (Q28263899) (← links)
- Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis (Q28267385) (← links)
- Dendritic changes in Alzheimer's disease and factors that may underlie these changes (Q28276894) (← links)
- Age-dependent induction of congophilic neurofibrillary tau inclusions in tau transgenic mice (Q28346155) (← links)
- Plasma neurofilament heavy chain levels correlate to markers of late stage disease progression and treatment response in SOD1(G93A) mice that model ALS (Q28481340) (← links)
- No requirement of alpha-internexin for nervous system development and for radial growth of axons (Q28506618) (← links)
- Late onset of motor neurons in mice overexpressing wild-type peripherin (Q28513274) (← links)
- Formation of intermediate filament protein aggregates with disparate effects in two transgenic mouse models lacking the neurofilament light subunit (Q28586151) (← links)
- Deficiency in ubiquitin ligase TRIM2 causes accumulation of neurofilament light chain and neurodegeneration (Q28588507) (← links)
- RNA-binding protein is involved in aggregation of light neurofilament protein and is implicated in the pathogenesis of motor neuron degeneration (Q28595098) (← links)
- Aldolases a and C are ribonucleolytic components of a neuronal complex that regulates the stability of the light-neurofilament mRNA. (Q33214481) (← links)
- Molecular mechanisms regulating motor neuron development and degeneration. (Q33737440) (← links)
- Neurofilament metabolism in sporadic amyotrophic lateral sclerosis. (Q33762430) (← links)
- Motor neuron disease--a review (Q33892039) (← links)
- Altered axonal architecture by removal of the heavily phosphorylated neurofilament tail domains strongly slows superoxide dismutase 1 mutant-mediated ALS. (Q33900561) (← links)
- Molecular factors underlying selective vulnerability of motor neurons to neurodegeneration in amyotrophic lateral sclerosis (Q33906246) (← links)
- Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E. (Q33935585) (← links)
- Alternative RNA splicing in the nervous system (Q33953763) (← links)
- Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration (Q33978879) (← links)
- Will antioxidants fulfill their expectations for the treatment of Alzheimer disease? (Q34038304) (← links)
- Cytoskeletal abnormalities in amyotrophic lateral sclerosis: beneficial or detrimental effects? (Q34088731) (← links)
- Nitric oxide-mediated oxidative damage and the progressive demise of motor neurons in ALS. (Q34092226) (← links)
- Reduced number of unmyelinated sensory axons in peripherin null mice (Q34133446) (← links)
- Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded (Q34175381) (← links)
- Multiple neuron-specific enhancers in the gene coding for the human neurofilament light chain (Q34368399) (← links)
- The cytoskeleton in neurodegenerative diseases (Q34446779) (← links)
- Expanding the phenotype associated with the NEFL mutation: neuromuscular disease in a family with overlapping myopathic and neurogenic findings. (Q34490328) (← links)
- Genetic rodent models of amyotrophic lateral sclerosis (Q34497123) (← links)
- Familial amyotrophic lateral sclerosis (Q34547620) (← links)
- Progress in the pathogenesis of amyotrophic lateral sclerosis (Q34566352) (← links)
- The genetic convergence of Charcot-Marie-Tooth disease types 1 and 2 and the role of genetics in sporadic neuropathy (Q34566690) (← links)
- Amyotrophic lateral sclerosis: human challenge for neuroscience (Q34598050) (← links)
- The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1. (Q34721268) (← links)
- Therapeutic developments in the treatment of amyotrophic lateral sclerosis (Q34974850) (← links)
- Inherited neuropathies (Q34997859) (← links)
- Pathways to motor neuron degeneration in transgenic mouse models (Q35069437) (← links)
- Functional complexity of intermediate filament cytoskeletons: from structure to assembly to gene ablation (Q35086651) (← links)
- Defective neurofilament transport in mouse models of amyotrophic lateral sclerosis: a review (Q35123882) (← links)
- The basic aspects of therapeutics in amyotrophic lateral sclerosis (Q35143367) (← links)
- Disease mechanisms in inherited neuropathies (Q35209953) (← links)
- E46K human alpha-synuclein transgenic mice develop Lewy-like and tau pathology associated with age-dependent, detrimental motor impairment (Q35266392) (← links)
- Molecular and cellular pathways of neurodegeneration in motor neurone disease (Q35489359) (← links)