scholarly article | Q13442814 |
P356 | DOI | 10.1111/BPA.12408 |
P698 | PubMed publication ID | 27338255 |
P50 | author | Iván Fernández-Vega | Q84286949 |
Margalida A Frau-Méndez | Q96006796 | ||
P2093 | author name string | Isidro Ferrer | |
Franc Llorens | |||
Inga Zerr | |||
Juan José Zarranz | |||
Belén Ansoleaga | |||
Jose Antonio Del Rio | |||
Margarita Carmona Tech | |||
Rosa Blanco Tech | |||
P2860 | cites work | The RIN: an RNA integrity number for assigning integrity values to RNA measurements | Q21263010 |
Function of nucleophosmin/B23, a nucleolar acidic protein, as a histone chaperone | Q24291795 | ||
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 | ||
The many roles of the eukaryotic elongation factor 1 complex | Q27003108 | ||
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene | Q28181555 | ||
Familial and sporadic fatal insomnia | Q28185765 | ||
Protein NPM3 interacts with the multifunctional nucleolar protein B23/nucleophosmin and inhibits ribosome biogenesis | Q28585849 | ||
Elongation factors in protein biosynthesis | Q34224585 | ||
Chromatin decondensation and nuclear reprogramming by nucleoplasmin | Q34353713 | ||
Nucleolin is a histone chaperone with FACT-like activity and assists remodeling of nucleosomes | Q34547435 | ||
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei | Q34692172 | ||
Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia. | Q35122319 | ||
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism | Q35138028 | ||
Proteomics analyses for the global proteins in the brain tissues of different human prion diseases | Q35325652 | ||
The elongation, termination, and recycling phases of translation in eukaryotes | Q36065893 | ||
New insights into the nucleophosmin/nucleoplasmin family of nuclear chaperones | Q36691603 | ||
Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis | Q37803365 | ||
Structural basis of the translational elongation cycle | Q38112829 | ||
NPM3, a member of the nucleophosmin/nucleoplasmin family, enhances activator-dependent transcription | Q39752067 | ||
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 patients | Q42273940 | ||
Interaction of nucleolin with ribosomal RNA genes and its role in RNA polymerase I transcription | Q42408640 | ||
Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation | Q43444644 | ||
Fatal familial insomnia: clinical and pathologic study of five new cases | Q43525616 | ||
Selection of novel reference genes for use in the human central nervous system: a BrainNet Europe Study | Q46348438 | ||
Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies. | Q46884646 | ||
Fatal familial insomnia: clinical features and molecular genetics | Q48174358 | ||
Fatal familial insomnia: Clinical features and early identification | Q48439556 | ||
Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion protein | Q48672330 | ||
Regional distribution of protease-resistant prion protein in fatal familial insomnia | Q48811338 | ||
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism | Q48882672 | ||
The thalamus participates in the regulation of the sleep-waking cycle. A clinico-pathological study in fatal familial thalamic degeneration | Q48939964 | ||
Fatal familial insomnia: behavioral and cognitive features. | Q52048639 | ||
P433 | issue | 1 | |
P921 | main subject | fatal familial insomnia | Q862872 |
P304 | page(s) | 95-106 | |
P577 | publication date | 2016-06-24 | |
P1433 | published in | Brain Pathology | Q4955776 |
P1476 | title | Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus | |
P478 | volume | 27 |
Q47107178 | Agrypnia excitata and obstructive apnea in a patient with fatal familial insomnia from China: A case report |
Q64057223 | Combinatory FK506 and Minocycline Treatment Alleviates Prion-Induced Neurodegenerative Events via Caspase-Mediated MAPK-NRF2 Pathway |
Q55220133 | Mutations Alter RNA-Mediated Conversion of Human Prions. |
Q47607995 | Sisyphus in Neverland |
Q58583990 | p62-Keap1-NRF2-ARE Pathway: A Contentious Player for Selective Targeting of Autophagy, Oxidative Stress and Mitochondrial Dysfunction in Prion Diseases |
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