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Thomas Ströbel

Showing results (1-10 of 47) with videos related to

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Amino Acids|June 14, 2011
Identification of c-myc-dependent proteins in the medulloblastoma cell line D425MedAmedeo A Azizi, Lin Li, Thomas Ströbel, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 19, 2015
Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain diseaseAnna S Berghoff, Anita Trummert, Ursula Unterberger, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 2013
Essential role for mammalian apurinic/apyrimidinic (AP) endonuclease Ape1/Ref-1 in telomere maintenanceSibylle Madlener, Thomas Ströbel, Sarah Vose, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 11, 2003
Level of Id-1 protein expression correlates with poor differentiation, enhanced malignant potential, and more aggressive clinical behavior of epithelial ovarian tumorsMonika Schindl, Sebastian F Schoppmann, Thomas Ströbel, et al.
Clinical Neuropathology|June 21, 2018
Molecular diagnostic testing of diffuse gliomas in the real-life setting: A practical approachMichał Bieńkowski, Adelheid Wöhrer, Patrizia Moser, et al.
Frontiers in Oncology|October 26, 2019
Circulating Tumor Biomarkers in Meningiomas Reveal a Signature of Equilibrium Between Tumor Growth and Immune ModulationErdogan Pekcan Erkan, Thomas Ströbel, Christian Dorfer, et al.
Acta Neuropathologica|September 13, 2005
Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivityEllen Gelpi, Gabor G Kovacs, Thomas Ströbel, et al.
Journal of Neuropathology and Experimental Neurology|July 11, 2007
Involvement of the endosomal-lysosomal system correlates with regional pathology in Creutzfeldt-Jakob diseaseGábor G Kovács, Ellen Gelpi, Thomas Ströbel, et al.
BMC Neurology|May 17, 2011
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 casesRobert Rusina, Gabor G Kovacs, Jindřich Fiala, et al.
Acta Neuropathologica|June 24, 2010
Four-repeat tauopathy clinically presenting as posterior cortical atrophy: atypical corticobasal degeneration?Kurt A Jellinger, Anja Grazer, Katja Petrovic, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Amino Acids|June 14, 2011
Identification of c-myc-dependent proteins in the medulloblastoma cell line D425MedAmedeo A Azizi, Lin Li, Thomas Ströbel, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 19, 2015
Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain diseaseAnna S Berghoff, Anita Trummert, Ursula Unterberger, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 2013
Essential role for mammalian apurinic/apyrimidinic (AP) endonuclease Ape1/Ref-1 in telomere maintenanceSibylle Madlener, Thomas Ströbel, Sarah Vose, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 11, 2003
Level of Id-1 protein expression correlates with poor differentiation, enhanced malignant potential, and more aggressive clinical behavior of epithelial ovarian tumorsMonika Schindl, Sebastian F Schoppmann, Thomas Ströbel, et al.
Clinical Neuropathology|June 21, 2018
Molecular diagnostic testing of diffuse gliomas in the real-life setting: A practical approachMichał Bieńkowski, Adelheid Wöhrer, Patrizia Moser, et al.
Frontiers in Oncology|October 26, 2019
Circulating Tumor Biomarkers in Meningiomas Reveal a Signature of Equilibrium Between Tumor Growth and Immune ModulationErdogan Pekcan Erkan, Thomas Ströbel, Christian Dorfer, et al.
Acta Neuropathologica|September 13, 2005
Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivityEllen Gelpi, Gabor G Kovacs, Thomas Ströbel, et al.
Journal of Neuropathology and Experimental Neurology|July 11, 2007
Involvement of the endosomal-lysosomal system correlates with regional pathology in Creutzfeldt-Jakob diseaseGábor G Kovács, Ellen Gelpi, Thomas Ströbel, et al.
BMC Neurology|May 17, 2011
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 casesRobert Rusina, Gabor G Kovacs, Jindřich Fiala, et al.
Acta Neuropathologica|June 24, 2010
Four-repeat tauopathy clinically presenting as posterior cortical atrophy: atypical corticobasal degeneration?Kurt A Jellinger, Anja Grazer, Katja Petrovic, et al.
Pageof 5