about
Identification of PEX7 as the second gene involved in Refsum diseaseTDP-43 mutations in familial and sporadic amyotrophic lateral sclerosisThe neuroprotective effects of heat shock protein 27 overexpression in transgenic animals against kainate-induced seizures and hippocampal cell deathHeat shock protein 27 rescues motor neurons following nerve injury and preserves muscle functionInvestigation of G72 (DAOA) expression in the human brain.Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidaseA new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2.The role of D-amino acids in amyotrophic lateral sclerosis pathogenesis: a review.Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder.CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.Mice that overexpress human heat shock protein 27 have increased renal injury following ischemia reperfusion.Heat shock protein 27 overexpression mitigates cytokine-induced islet apoptosis and streptozotocin-induced diabetes.Pathogenesis of Parkinson's disease: emerging role of molecular chaperones.
P50
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P50
description
onderzoeker
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name
Jacqueline de Belleroche
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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type
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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Jacqueline de Belleroche
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