Works matching IS 00016322 AND DT 2022 AND VI 144 AND IP 4
Results: 14
Transmission of cervid prions to humanized mice demonstrates the zoonotic potential of CWD.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 767, doi. 10.1007/s00401-022-02482-9
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Rainwater Charitable Foundation criteria for the neuropathologic diagnosis of progressive supranuclear palsy.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 603, doi. 10.1007/s00401-022-02479-4
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Single-cell DNA sequencing reveals order of mutational acquisition in TRAF7/AKT1 and TRAF7/KLF4 mutant meningiomas.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 799, doi. 10.1007/s00401-022-02485-6
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Single-nucleus chromatin accessibility profiling highlights distinct astrocyte signatures in progressive supranuclear palsy and corticobasal degeneration.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 615, doi. 10.1007/s00401-022-02483-8
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DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt–Jakob disease.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 785, doi. 10.1007/s00401-022-02481-w
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Selective tau seeding assays and isoform-specific antibodies define neuroanatomic distribution of progressive supranuclear palsy pathology arising in Alzheimer's disease.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 789, doi. 10.1007/s00401-022-02480-x
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Molecular classification and outcome of children with rare CNS embryonal tumors: results from St. Jude Children's Research Hospital including the multi-center SJYC07 and SJMB03 clinical trials.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 733, doi. 10.1007/s00401-022-02484-7
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Multiplatform molecular analyses refine classification of gliomas arising in patients with neurofibromatosis type 1.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 747, doi. 10.1007/s00401-022-02478-5
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Spatiotemporal characterization of cellular tau pathology in the human locus coeruleus–pericoerulear complex by three-dimensional imaging.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 651, doi. 10.1007/s00401-022-02477-6
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Multiple system atrophy prions transmit neurological disease to mice expressing wild-type human α-synuclein.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 677, doi. 10.1007/s00401-022-02476-7
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Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 707, doi. 10.1007/s00401-022-02475-8
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- Article
Flow blockage disrupts cilia-driven fluid transport in the epileptic brain.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 691, doi. 10.1007/s00401-022-02463-y
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- Article
Loss of LAMP5 interneurons drives neuronal network dysfunction in Alzheimer's disease.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 637, doi. 10.1007/s00401-022-02457-w
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Generation of patient-derived models from a metastatic pediatric diffuse leptomeningeal glioneuronal tumor with KIAA1549::BRAF fusion.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 793, doi. 10.1007/s00401-022-02473-w
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