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Olaf Riess

Showing results (151-160 of 313) with videos related to

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Cancer Research|May 19, 2006
Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysisChristina S Schuetz, Michael Bonin, Susan E Clare, et al.
Cancers|August 23, 2020
Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma PatientsFranz J Hilke, Tobias Sinnberg, Axel Gschwind, et al.
Frontiers in Immunology|March 25, 2026
Dysregulated NK-cell gene expression defines the enduring symptoms of long COVID-19Urvi Ray, Antje Schulze Selting, Roshan Priyarangana Perera, et al.
Cerebrovascular Diseases (Basel, Switzerland)|December 24, 2010
Protocol and methodology of the Stroke in Young Fabry Patients (sifap1) study: a prospective multicenter European study of 5,024 young stroke patients aged 18-55 yearsArndt Rolfs, Peter Martus, Peter U Heuschmann, et al.
Investigative Ophthalmology & Visual Science|September 10, 2009
In vivo analysis of cone survival in miceSusanne C Beck, Karin Schaeferhoff, Stylianos Michalakis, et al.
Neuroimage|August 26, 2006
Expression mapping of tetracycline-responsive prion protein promoter: digital atlasing for generating cell-specific disease modelsJana Boy, Trygve B Leergaard, Thorsten Schmidt, et al.
Bone|June 24, 2018
Novel WNT1 mutations in children with osteogenesis imperfecta: Clinical and functional characterizationYanqin Lu, Xiuzhi Ren, Yanzhou Wang, et al.
Neuroscience Letters|October 30, 2003
Mutation analysis of the neurofilament M gene in Parkinson's diseaseRejko Krüger, Christian Fischer, Thorsten Schulte, et al.
Experimental Neurology|May 31, 2008
Parkinson patient fibroblasts show increased alpha-synuclein expressionHans-Hermann Hoepken, Suzana Gispert, Mekhman Azizov, et al.
European Journal of Human Genetics : EJHG|May 8, 2014
Genome-wide UPD screening in patients with intellectual disabilityChristopher Schroeder, Arif Bülent Ekici, Ute Moog, et al.
Pageof 32

Showing results (151-160 of 313) with videos related to

Sort By:
Pageof 32
Cancer Research|May 19, 2006
Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysisChristina S Schuetz, Michael Bonin, Susan E Clare, et al.
Cancers|August 23, 2020
Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma PatientsFranz J Hilke, Tobias Sinnberg, Axel Gschwind, et al.
Frontiers in Immunology|March 25, 2026
Dysregulated NK-cell gene expression defines the enduring symptoms of long COVID-19Urvi Ray, Antje Schulze Selting, Roshan Priyarangana Perera, et al.
Cerebrovascular Diseases (Basel, Switzerland)|December 24, 2010
Protocol and methodology of the Stroke in Young Fabry Patients (sifap1) study: a prospective multicenter European study of 5,024 young stroke patients aged 18-55 yearsArndt Rolfs, Peter Martus, Peter U Heuschmann, et al.
Investigative Ophthalmology & Visual Science|September 10, 2009
In vivo analysis of cone survival in miceSusanne C Beck, Karin Schaeferhoff, Stylianos Michalakis, et al.
Neuroimage|August 26, 2006
Expression mapping of tetracycline-responsive prion protein promoter: digital atlasing for generating cell-specific disease modelsJana Boy, Trygve B Leergaard, Thorsten Schmidt, et al.
Bone|June 24, 2018
Novel WNT1 mutations in children with osteogenesis imperfecta: Clinical and functional characterizationYanqin Lu, Xiuzhi Ren, Yanzhou Wang, et al.
Neuroscience Letters|October 30, 2003
Mutation analysis of the neurofilament M gene in Parkinson's diseaseRejko Krüger, Christian Fischer, Thorsten Schulte, et al.
Experimental Neurology|May 31, 2008
Parkinson patient fibroblasts show increased alpha-synuclein expressionHans-Hermann Hoepken, Suzana Gispert, Mekhman Azizov, et al.
European Journal of Human Genetics : EJHG|May 8, 2014
Genome-wide UPD screening in patients with intellectual disabilityChristopher Schroeder, Arif Bülent Ekici, Ute Moog, et al.
Pageof 32