Notch-1 activation and dendritic atrophy in prion disease. - Wikidata - awgldk - TriplyDB

Notch-1 activation and dendritic atrophy in prion disease.

Notch-1 activation and dendritic atrophy in prion disease.

http://www.wikidata.org/entity/Q33756871

about

Neuronal regeneration in a zebrafish model of adult brain injury A systems approach to prion disease Impaired axonal transport in motor neurons correlates with clinical prion disease Identification of genetic modifiers of TDP-43 neurotoxicity in Drosophila Regulation of mammalian Notch signaling and embryonic development by the protein O-glucosyltransferase Rumi hnRNP I inhibits Notch signaling and regulates intestinal epithelial homeostasis in the zebrafish.Convection-enhanced delivery of AAV2-PrPshRNA in prion-infected mice Stress-induced switch in Numb isoforms enhances Notch-dependent expression of subtype-specific transient receptor potential channel.PrPSc accumulation in neuronal plasma membranes links Notch-1 activation to dendritic degeneration in prion diseases.Granzyme B-induced neurotoxicity is mediated via activation of PAR-1 receptor and Kv1.3 channel.Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease The intricate mechanisms of neurodegeneration in prion diseases.Notch and PKC are involved in formation of the lateral region of the dorso-ventral axis in Drosophila embryos.Not(ch) just development: Notch signalling in the adult brain.Continuum of prion protein structures enciphers a multitude of prion isolate-specified phenotypes.Therapeutic effect of CHF5074, a new γ-secretase modulator, in a mouse model of scrapie.Conditional deletion of Notch1 and Notch2 genes in excitatory neurons of postnatal forebrain does not cause neurodegeneration or reduction of Notch mRNAs and proteins Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders.TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways.Diffuse abnormality of low to moderately organized white matter in schizophrenia.A gamma-secretase inhibitor and quinacrine reduce prions and prevent dendritic degeneration in murine brains Prion diseases: from protein to cell pathology.Correlating DWI MRI with pathologic and other features of Jakob-Creutzfeldt disease Molecular pathology of human prion diseases.Cryo-immunogold electron microscopy for prions: toward identification of a conversion site.CRMPs: critical molecules for neurite morphogenesis and neuropsychiatric diseases.Overstimulation of PrPC signaling pathways by prion peptide 106-126 causes oxidative injury of bioaminergic neuronal cells.mTORC1 activation in podocytes is a critical step in the development of diabetic nephropathy in mice.The Notch-1 intracellular domain is found in sub-nuclear bodies in SH-SY5Y neuroblastomas and in primary cortical neurons Developmental influence of the cellular prion protein on the gene expression profile in mouse hippocampus.Notch1 cardioprotection in myocardial ischemia/reperfusion involves reduction of oxidative/nitrative stress.Autobiography Series: From Sleep-Wake Mechanisms to Prion Diseases.

P2860

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P2860

Notch-1 activation and dendritic atrophy in prion disease.

http://www.wikidata.org/entity/Q33756871

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2005 nî lūn-bûn

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2005 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2005 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2005年の論文

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2005年論文

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2005年論文

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2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

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name

Notch-1 activation and dendritic atrophy in prion disease.

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Notch-1 activation and dendritic atrophy in prion disease.

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type

label

Notch-1 activation and dendritic atrophy in prion disease.

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Notch-1 activation and dendritic atrophy in prion disease.

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prefLabel

Notch-1 activation and dendritic atrophy in prion disease.

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Notch-1 activation and dendritic atrophy in prion disease.

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PNAS.0408612101

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Notch-1 activation and dendritic atrophy in prion disease.

@en

P2093

Eric J Huang

http://www.w3.org/2001/XMLSchema#string

Erik Samayoa

http://www.w3.org/2001/XMLSchema#string

Essia Bouzamondo-Bernstein

http://www.w3.org/2001/XMLSchema#string

Jared L Clever

http://www.w3.org/2001/XMLSchema#string

Nako Ishikura

http://www.w3.org/2001/XMLSchema#string

P2860

Prion Protein Biology

[URE3] as an altered URE2 protein: evidence for a prion analog in Saccharomyces cerevisiae

Strain-specified relative conformational stability of the scrapie prion protein

A model for Ure2p prion filaments and other amyloids: the parallel superpleated beta-structure

Targeted deletion of numb and numblike in sensory neurons reveals their essential functions in axon arborization

Eight prion strains have PrP(Sc) molecules with different conformations

Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

Nuclear Notch1 signaling and the regulation of dendritic development.

Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice.

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886-891

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10.1073/PNAS.0408612101

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3

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102

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Stanley B. Prusiner

Stephen J DeArmond

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2005-01-07T00:00:00Z

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P5875

8091694

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P698

15640354

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P921

Prion protein family

P932

545568

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