213 results on '"Ströbel, Thomas"'
Search Results
2. Neuropathology-driven Whole-genome Sequencing Study Points to Novel Candidate Genes for Healthy Brain Aging
3. Dura mater is a potential source of Aβ seeds
4. Cerebellar dysfunction in a family harboring the PSEN1 mutation co-segregating with a Cathepsin D variant p.A58V
5. Genetically Engineered Microvesicles Carrying Suicide mRNA/Protein Inhibit Schwannoma Tumor Growth
6. Essential role for mammalian apurinic/apyrimidinic (AP) endonuclease Ape1/Ref-1 in telomere maintenance
7. Tau pathology in Creutzfeldt‐Jakob disease revisited
8. Influence of MMR, MGMT Promotor Methylation and Protein Expression on Overall and Progression-Free Survival in Primary Glioblastoma Patients Treated with Temozolomide.
9. miR-1289 and “Zipcode”-like Sequence Enrich mRNAs in Microvesicles
10. SRPX Emerges as a Potential Tumor Marker in the Extracellular Vesicles of Glioblastoma
11. SNP-array based whole genome homozygosity mapping: A quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients
12. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
13. Clinicopathological description of two cases with SQSTM1 gene mutation associated with frontotemporal dementia
14. Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease
15. A case of variably protease-sensitive prionopathy treated with doxycyclin
16. Interlaboratory comparison of IDH mutation detection
17. Histotype-Dependent Oligodendroglial PrP Pathology in Sporadic CJD: A Frequent Feature of the M2C “Strain”
18. Identification of c-myc-dependent proteins in the medulloblastoma cell line D425Med
19. A peculiar constellation of tau pathology defines a subset of dementia in the elderly
20. Four-repeat tauopathy clinically presenting as posterior cortical atrophy: atypical corticobasal degeneration?
21. Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy
22. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity
23. A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
24. The medulloblastoma cell line DAOY but not eleven other tumor cell lines expresses minichromosome maintenance protein 4
25. Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease
26. Mitochondrial respiratory chain deficiency correlates with the severity of neuropathology in sporadic Creutzfeldt-Jakob disease
27. Inter-Laboratory Assessment of PrPSc Typing in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium
28. Involvement of the Endosomal-Lysosomal System Correlates With Regional Pathology in Creutzfeldt-Jakob Disease
29. Effects of Formalin Fixation, Paraffin Embedding, and Time of Storage on DNA Preservation in Brain Tissue: A BrainNet Europe Study
30. Brain Protein Preservation Largely Depends on the Postmortem Storage Temperature: Implications for Study of Proteins in Human Neurologic Diseases and Management of Brain Banks: A BrainNet Europe Study
31. Complement activation in human prion disease
32. Fibroblasts Can Express Glial Fibrillary Acidic Protein (GFAP) In Vivo
33. Circulating Tumor Biomarkers in Meningiomas Reveal a Signature of Equilibrium Between Tumor Growth and Immune Modulation
34. FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases
35. High expression of DNA topoisomerase IIα and Ki-67 antigen is associated with prolonged survival in glioblastoma patients
36. Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease.
37. Tau Pathology in Creutzfeldt-Jakob Disease Revisited
38. Familial early-onset dementia with complex neuropathologic phenotype and genomic background
39. Molecular diagnostic testing of diffuse gliomas in the real-life setting: A practical approach
40. Ape1 guides DNA repair pathway choice that is associated with drug tolerance in glioblastoma
41. The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
42. TECPR2 a positive regulator of autophagy is implicated in healthy brain ageing
43. Overexpression of minichromosome maintenance protein 10 in medulloblastoma and its clinical implications
44. Tau pathology in Creutzfeldt-Jakob disease revisited
45. KINFix – A formalin-free non-commercial fixative optimized for histological, immunohistochemical and molecular analyses of neurosurgical tissue specimens
46. A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk
47. Clinicopathological description of two cases withSQSTM1gene mutation associated with frontotemporal dementia
48. A Genome Wide Association Study Links Glutamate Receptor Pathway to Sporadic Creutzfeldt-Jakob Disease Risk
49. Genomic Alterations in Atypical Teratoid/Rhabdoid Tumors: The Medical University of Vienna Experience
50. Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?
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