Pages that link to "Q21469470"
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The following pages link to Christopher Shaw (Q21469470):
Displaying 50 items.
- Christopher Shaw (Q24005568) (← links)
- VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis (Q24298739) (← links)
- ALS2/Alsin regulates Rac-PAK signaling and neurite outgrowth (Q24310305) (← links)
- Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (Q24612662) (← links)
- Natural history and clinical features of the flail arm and flail leg ALS variants (Q24647753) (← links)
- The Progressive BSSG Rat Model of Parkinson's: Recapitulating Multiple Key Features of the Human Disease (Q27315090) (← links)
- Proteomic analyses reveal that loss of TDP-43 affects RNA processing and intracellular transport (Q28115707) (← links)
- Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6 (Q28236805) (← links)
- TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis (Q28270779) (← links)
- Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice (Q28274767) (← links)
- NEK1 variants confer susceptibility to amyotrophic lateral sclerosis (Q28277378) (← links)
- Aluminum-induced entropy in biological systems: implications for neurological disease (Q28396107) (← links)
- Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis (Q28473603) (← links)
- Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease (Q28748461) (← links)
- A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis (Q29417136) (← links)
- Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease (Q29614879) (← links)
- Environmental neurotoxin-induced progressive model of parkinsonism in rats (Q30497416) (← links)
- ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43. (Q30536540) (← links)
- Astrocyte pathology and the absence of non-cell autonomy in an induced pluripotent stem cell model of TDP-43 proteinopathy. (Q30537986) (← links)
- Differential roles of the ubiquitin proteasome system and autophagy in the clearance of soluble and aggregated TDP-43 species (Q30574024) (← links)
- Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS. (Q30655551) (← links)
- The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci (Q30975356) (← links)
- An evaluation of a SVA retrotransposon in the FUS promoter as a transcriptional regulator and its association to ALS (Q31153726) (← links)
- Parkinson-dementia complex and development of a new stable isotope dilution assay for BMAA detection in tissue (Q33498266) (← links)
- Latent cluster analysis of ALS phenotypes identifies prognostically differing groups (Q33505666) (← links)
- Progranulin is expressed within motor neurons and promotes neuronal cell survival (Q33513028) (← links)
- Nuclear import impairment causes cytoplasmic trans-activation response DNA-binding protein accumulation and is associated with frontotemporal lobar degeneration (Q33578925) (← links)
- Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration (Q33644364) (← links)
- The primary locus of motor neuron death in an ALS-PDC mouse model (Q33644388) (← links)
- Distribution of free and glycosylated sterols within Cycas micronesica plants (Q33649475) (← links)
- A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories (Q33658563) (← links)
- Phenotypic Characteristics as Predictors of Phytosterols in Mature Cycas micronesica Seeds. (Q33668638) (← links)
- An estimate of amyotrophic lateral sclerosis heritability using twin data. (Q33699565) (← links)
- Endosomal accumulation of APP in wobbler motor neurons reflects impaired vesicle trafficking: implications for human motor neuron disease (Q33840151) (← links)
- Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase (Q33842154) (← links)
- Tau levels do not influence human ALS or motor neuron degeneration in the SOD1G93A mouse. (Q33899853) (← links)
- Autophagy induction enhances TDP43 turnover and survival in neuronal ALS models. (Q33930825) (← links)
- The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease (Q33986970) (← links)
- Aluminum vaccine adjuvants: are they safe? (Q34026879) (← links)
- Human papillomavirus (HPV) vaccine policy and evidence-based medicine: are they at odds? (Q34029941) (← links)
- Reduction in hSOD1 copy number significantly impacts ALS phenotype presentation in G37R (line 29) mice: implications for the assessment of putative therapeutic agents (Q34051858) (← links)
- C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis (Q34063137) (← links)
- Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis (Q34173712) (← links)
- Cholesteryl Glucoside Stimulates Activation of Protein Kinase B/Akt in the Motor Neuron-Derived NSC34 Cell Line (Q34179036) (← links)
- Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. (Q34235637) (← links)
- Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. (Q34295566) (← links)
- Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study (Q34340508) (← links)
- Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72 (Q34500097) (← links)
- Behavioral abnormalities in female mice following administration of aluminum adjuvants and the human papillomavirus (HPV) vaccine Gardasil (Q34677865) (← links)
- Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (Q34682478) (← links)