Search research articles
Contact Us
Filters
Showing results (171-180 of 358) with videos related to
Page
of 36
Sort By:
Applied Microbiology and Biotechnology
|
September 19, 2017
Molecular basis of Cd<sup>+2</sup> stress response in Candida tropicalis
Zaman Khan, Abdul Rehman, Muhammad Atif Nisar, et al.
Molecular Neurobiology
|
May 10, 2014
Characteristic CSF prion seeding efficiency in humans with prion diseases
Maria Cramm, Matthias Schmitz, André Karch, et al.
Neurobiology of Aging
|
July 15, 2015
Cytokine profiles and the role of cellular prion protein in patients with vascular dementia and vascular encephalopathy
Matthias Schmitz, Peter Hermann, Pantelis Oikonomou, et al.
Acta Neuropathologica Communications
|
February 10, 2026
Alterations in cerebrospinal fluid levels of myelin- and oligodendrocyte-related proteins in sporadic Creutzfeldt-Jakob disease
Fabian Maass, Carolina Thomas, Lille Kurvits, et al.
Journal of Molecular Neuroscience : MN
|
September 6, 2017
MicroRNA Expression in the Locus Coeruleus, Entorhinal Cortex, and Hippocampus at Early and Middle Stages of Braak Neurofibrillary Tangle Pathology
Franc Llorens, Katrin Thüne, Pol Andrés-Benito, et al.
Expert Review of Molecular Diagnostics
|
September 13, 2019
The cellular prion protein and its derived fragments in human prion diseases and their role as potential biomarkers
Katrin Thüne, Matthias Schmitz, Anna Villar-Piqué, et al.
Molecular Neurobiology
|
November 18, 2025
Proteomic Profiling Reveals Mitochondrial Dysregulation in Rapidly Progressive Alzheimer's: Role of DLDH in Amyloid Beta Aggregation
Saima Zafar, Aneeqa Noor, Neelam Younas, et al.
Journal of Proteome Research
|
September 28, 2010
Codon 129 polymorphism specific cerebrospinal fluid proteome pattern in sporadic Creutzfeldt-Jakob disease and the implication of glycolytic enzymes in prion-induced pathology
Joanna Gawinecka, Jana Dieks, Abdul R Asif, et al.
Acta Neuropathologica
|
June 20, 2007
A novel subtype of Creutzfeldt-Jakob disease characterized by a small 6 kDa PrP fragment
Bjarne Krebs, Benedikt Bader, Juliane Klehmet, et al.
Journal of Neuropathology and Experimental Neurology
|
June 15, 2016
Altered Mitochondria, Protein Synthesis Machinery, and Purine Metabolism Are Molecular Contributors to the Pathogenesis of Creutzfeldt-Jakob Disease
Belén Ansoleaga, Paula Garcia-Esparcia, Franc Llorens, et al.
Page
of 36
Search research articles
Search
Showing results (171-180 of 358) with videos related to
Sort By:
Page
of 36
Applied Microbiology and Biotechnology
|
September 19, 2017
Molecular basis of Cd<sup>+2</sup> stress response in Candida tropicalis
Zaman Khan, Abdul Rehman, Muhammad Atif Nisar, et al.
Molecular Neurobiology
|
May 10, 2014
Characteristic CSF prion seeding efficiency in humans with prion diseases
Maria Cramm, Matthias Schmitz, André Karch, et al.
Neurobiology of Aging
|
July 15, 2015
Cytokine profiles and the role of cellular prion protein in patients with vascular dementia and vascular encephalopathy
Matthias Schmitz, Peter Hermann, Pantelis Oikonomou, et al.
Acta Neuropathologica Communications
|
February 10, 2026
Alterations in cerebrospinal fluid levels of myelin- and oligodendrocyte-related proteins in sporadic Creutzfeldt-Jakob disease
Fabian Maass, Carolina Thomas, Lille Kurvits, et al.
Journal of Molecular Neuroscience : MN
|
September 6, 2017
MicroRNA Expression in the Locus Coeruleus, Entorhinal Cortex, and Hippocampus at Early and Middle Stages of Braak Neurofibrillary Tangle Pathology
Franc Llorens, Katrin Thüne, Pol Andrés-Benito, et al.
Expert Review of Molecular Diagnostics
|
September 13, 2019
The cellular prion protein and its derived fragments in human prion diseases and their role as potential biomarkers
Katrin Thüne, Matthias Schmitz, Anna Villar-Piqué, et al.
Molecular Neurobiology
|
November 18, 2025
Proteomic Profiling Reveals Mitochondrial Dysregulation in Rapidly Progressive Alzheimer's: Role of DLDH in Amyloid Beta Aggregation
Saima Zafar, Aneeqa Noor, Neelam Younas, et al.
Journal of Proteome Research
|
September 28, 2010
Codon 129 polymorphism specific cerebrospinal fluid proteome pattern in sporadic Creutzfeldt-Jakob disease and the implication of glycolytic enzymes in prion-induced pathology
Joanna Gawinecka, Jana Dieks, Abdul R Asif, et al.
Acta Neuropathologica
|
June 20, 2007
A novel subtype of Creutzfeldt-Jakob disease characterized by a small 6 kDa PrP fragment
Bjarne Krebs, Benedikt Bader, Juliane Klehmet, et al.
Journal of Neuropathology and Experimental Neurology
|
June 15, 2016
Altered Mitochondria, Protein Synthesis Machinery, and Purine Metabolism Are Molecular Contributors to the Pathogenesis of Creutzfeldt-Jakob Disease
Belén Ansoleaga, Paula Garcia-Esparcia, Franc Llorens, et al.
Page
of 36