Works matching IS 00016322 AND DT 2013 AND VI 125 AND IP 3
Results: 14
OTX2 sustains a bivalent-like state of OTX2-bound promoters in medulloblastoma by maintaining their H3K27me3 levels.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 385, doi. 10.1007/s00401-012-1069-2
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- Publication type:
- Article
Aberrant patterns of H3K4 and H3K27 histone lysine methylation occur across subgroups in medulloblastoma.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 373, doi. 10.1007/s00401-012-1070-9
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- Publication type:
- Article
Polymorphonuclear neutrophil infiltration into ischemic infarctions: myth or truth?
- Published in:
- 2013
- By:
- Publication type:
- Editorial
Erratum to: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38.
- Published in:
- 2013
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- Publication type:
- Correction Notice
Nervous system involvement in von Hippel-Lindau disease: pathology and mechanisms.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 333, doi. 10.1007/s00401-013-1091-z
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- Publication type:
- Article
Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 351, doi. 10.1007/s00401-013-1093-x
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- Publication type:
- Article
DNA methylation profiling of medulloblastoma allows robust subclassification and improved outcome prediction using formalin-fixed biopsies.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 359, doi. 10.1007/s00401-012-1077-2
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- Publication type:
- Article
hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 413, doi. 10.1007/s00401-013-1088-7
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- Publication type:
- Article
Lysosomal storage and advanced senescence in the brain of LAMP-2-deficient Danon disease.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Evolving neurobiology of tuberous sclerosis complex.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 317, doi. 10.1007/s00401-013-1085-x
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- Publication type:
- Article
Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 425, doi. 10.1007/s00401-012-1059-4
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- Publication type:
- Article
VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 439, doi. 10.1007/s00401-012-1073-6
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- Publication type:
- Article
The neurovascular unit as a selective barrier to polymorphonuclear granulocyte (PMN) infiltration into the brain after ischemic injury.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 3, p. 395, doi. 10.1007/s00401-012-1076-3
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- Publication type:
- Article