Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus

scientific article

Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/BPA.12408
P698PubMed publication ID27338255

P50authorIván Fernández-VegaQ84286949
Margalida A Frau-MéndezQ96006796
P2093author name stringIsidro Ferrer
Franc Llorens
Inga Zerr
Juan José Zarranz
Belén Ansoleaga
Jose Antonio Del Rio
Margarita Carmona Tech
Rosa Blanco Tech
P2860cites workThe RIN: an RNA integrity number for assigning integrity values to RNA measurementsQ21263010
Function of nucleophosmin/B23, a nucleolar acidic protein, as a histone chaperoneQ24291795
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The many roles of the eukaryotic elongation factor 1 complexQ27003108
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein geneQ28181555
Familial and sporadic fatal insomniaQ28185765
Protein NPM3 interacts with the multifunctional nucleolar protein B23/nucleophosmin and inhibits ribosome biogenesisQ28585849
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Nucleolin is a histone chaperone with FACT-like activity and assists remodeling of nucleosomesQ34547435
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nucleiQ34692172
Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.Q35122319
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphismQ35138028
Proteomics analyses for the global proteins in the brain tissues of different human prion diseasesQ35325652
The elongation, termination, and recycling phases of translation in eukaryotesQ36065893
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Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesisQ37803365
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NPM3, a member of the nucleophosmin/nucleoplasmin family, enhances activator-dependent transcriptionQ39752067
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.Q40537014
Comparative analysis of gene expression profiles between cortex and thalamus in Chinese fatal familial insomnia patientsQ42273940
Interaction of nucleolin with ribosomal RNA genes and its role in RNA polymerase I transcriptionQ42408640
Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutationQ43444644
Fatal familial insomnia: clinical and pathologic study of five new casesQ43525616
Selection of novel reference genes for use in the human central nervous system: a BrainNet Europe StudyQ46348438
Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies.Q46884646
Fatal familial insomnia: clinical features and molecular geneticsQ48174358
Fatal familial insomnia: Clinical features and early identificationQ48439556
Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion proteinQ48672330
Regional distribution of protease-resistant prion protein in fatal familial insomniaQ48811338
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphismQ48882672
The thalamus participates in the regulation of the sleep-waking cycle. A clinico-pathological study in fatal familial thalamic degenerationQ48939964
Fatal familial insomnia: behavioral and cognitive features.Q52048639
P433issue1
P921main subjectfatal familial insomniaQ862872
P304page(s)95-106
P577publication date2016-06-24
P1433published inBrain PathologyQ4955776
P1476titleFatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus
P478volume27

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cites work (P2860)
Q47107178Agrypnia excitata and obstructive apnea in a patient with fatal familial insomnia from China: A case report
Q64057223Combinatory FK506 and Minocycline Treatment Alleviates Prion-Induced Neurodegenerative Events via Caspase-Mediated MAPK-NRF2 Pathway
Q55220133Mutations Alter RNA-Mediated Conversion of Human Prions.
Q47607995Sisyphus in Neverland
Q58583990p62-Keap1-NRF2-ARE Pathway: A Contentious Player for Selective Targeting of Autophagy, Oxidative Stress and Mitochondrial Dysfunction in Prion Diseases

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