about
A YAC contig encompassing the XRCC5 (Ku80) DNA repair gene and complementation of defective cells by YAC protoplast fusionMutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaMouse cytoplasmic dynein intermediate chains: identification of new isoforms, alternative splicing and tissue distribution of transcriptsThe legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease.Intermediate chain subunit as a probe for cytoplasmic dynein function: biochemical analyses and live cell imaging in PC12 cells.A comprehensive assessment of the SOD1G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosis.Behavioral and other phenotypes in a cytoplasmic Dynein light intermediate chain 1 mutant mouse.The kinesin light chain gene: its mapping and exclusion in mouse and human forms of inherited motor neuron degeneration.Mitochondrial protein-linked DNA breaks perturb mitochondrial gene transcription and trigger free radical-induced DNA damage.SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice.Expression of a pathogenic mutation of SOD1 sensitizes aprataxin-deficient cells and mice to oxidative stress and triggers hallmarks of premature ageing.PARP-1 dependent recruitment of the amyotrophic lateral sclerosis-associated protein FUS/TLS to sites of oxidative DNA damage.Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophyMouse models for neurological disease.A mutation in dynein rescues axonal transport defects and extends the life span of ALS miceCytoplasmic dynein heavy chain: the servant of many mastersNeurobiology of axonal transport defects in motor neuron diseases: Opportunities for translational research?An extended panel of hamster-human hybrids for chromosome 2q.Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues.Binding of dynein intermediate chain 2 to paxillin controls focal adhesion dynamics and migration.From the cell membrane to the nucleus: unearthing transport mechanisms for dynein.DYNC1H1 mutation alters transport kinetics and ERK1/2-cFos signalling in a mouse model of distal spinal muscular atrophy.Mutations in dynein link motor neuron degeneration to defects in retrograde transportThe phagocytic capacity of neuronesNo association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disordersGenetic Insights into Mammalian Cytoplasmic Dynein Function Provided by Novel Mutations in the MouseThe SOD1 transgene in the G93A mouse model of amyotrophic lateral sclerosis lies on distal mouse chromosome 12FUS (fused in sarcoma) is a component of the cellular response to topoisomerase I-induced DNA breakage and transcriptional stressA hamster-human subchromosomal hybrid cell panel for chromosome 2Caspases and neurodegenerative diseasesComplementation analysis of testis tumor cellsDynein-dynactin complex subunits are differentially localized in brain and spinal cord, with selective involvement in pathological features of neurodegenerative diseasePrion disease incubation time is not affected in mice heterozygous for a dynein mutationPotential of activated microglia as a source of dysregulated extracellular microRNAs contributing to neurodegeneration in amyotrophic lateral sclerosis
P50
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P50
description
onderzoeker
@nl
researcher
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հետազոտող
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name
Majid Hafezparast
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Majid Hafezparast
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Majid Hafezparast
@es
Majid Hafezparast
@nl
type
label
Majid Hafezparast
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Majid Hafezparast
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Majid Hafezparast
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Majid Hafezparast
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prefLabel
Majid Hafezparast
@ast
Majid Hafezparast
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Majid Hafezparast
@es
Majid Hafezparast
@nl
P106
P1153
55991366400
P31
P496
0000-0002-5262-7150