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F Bronner

Showing results (61-70 of 76) with videos related to

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Archives Des Maladies Du Coeur Et Des Vaisseaux|November 24, 1999
[Value of the analysis of pulmonary venous flow in the evaluation of hemodynamics in dialysed patients]M Schneeberger, M P Douchet, F Chantrel, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 20, 1999
[Paradoxal lowering of parasympathetic indices in myasthenic patients]M P Douchet, E Quiring, F Bronner, et al.
Plos One|August 29, 2009
Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathwaysIraad F Bronner, Zoltán Bochdanovits, Patrizia Rizzu, et al.
Annales De Cardiologie Et D'Angeiologie|November 11, 1998
[Variability of heart rate after heart surgery under extracorporeal circulation: aortocoronary bypass or aortic valve replacement]F Bronner, M P Douchet, E Quiring, et al.
Acta Neuropathologica Communications|March 20, 2019
Assembly of transgenic human P301S Tau is necessary for neurodegeneration in murine spinal cordJennifer A Macdonald, Iraad F Bronner, Lesley Drynan, et al.
Human Molecular Genetics|September 4, 2003
The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexesMaria G Macedo, Burcu Anar, Iraad F Bronner, et al.
Pacing and Clinical Electrophysiology : PACE|November 24, 1998
Optimizing the hemodynamic performance of the DDD pacemaker: impact of the atrioventricular delay on the pulmonary venous flow patternM P Douchet, E Quiring, R Vi-Fane, et al.
Journal of Neuropathology and Experimental Neurology|January 6, 2007
The DeltaK280 mutation in MAP tau favors exon 10 skipping in vivoJohn C van Swieten, Iraad F Bronner, Asma Azmani, et al.
Brain : a Journal of Neurology|July 15, 2005
Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathologyI F Bronner, B C ter Meulen, A Azmani, et al.
Genome Research|May 20, 2016
Quantitative insertion-site sequencing (QIseq) for high throughput phenotyping of transposon mutantsIraad F Bronner, Thomas D Otto, Min Zhang, et al.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
Archives Des Maladies Du Coeur Et Des Vaisseaux|November 24, 1999
[Value of the analysis of pulmonary venous flow in the evaluation of hemodynamics in dialysed patients]M Schneeberger, M P Douchet, F Chantrel, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 20, 1999
[Paradoxal lowering of parasympathetic indices in myasthenic patients]M P Douchet, E Quiring, F Bronner, et al.
Plos One|August 29, 2009
Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathwaysIraad F Bronner, Zoltán Bochdanovits, Patrizia Rizzu, et al.
Annales De Cardiologie Et D'Angeiologie|November 11, 1998
[Variability of heart rate after heart surgery under extracorporeal circulation: aortocoronary bypass or aortic valve replacement]F Bronner, M P Douchet, E Quiring, et al.
Acta Neuropathologica Communications|March 20, 2019
Assembly of transgenic human P301S Tau is necessary for neurodegeneration in murine spinal cordJennifer A Macdonald, Iraad F Bronner, Lesley Drynan, et al.
Human Molecular Genetics|September 4, 2003
The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexesMaria G Macedo, Burcu Anar, Iraad F Bronner, et al.
Pacing and Clinical Electrophysiology : PACE|November 24, 1998
Optimizing the hemodynamic performance of the DDD pacemaker: impact of the atrioventricular delay on the pulmonary venous flow patternM P Douchet, E Quiring, R Vi-Fane, et al.
Journal of Neuropathology and Experimental Neurology|January 6, 2007
The DeltaK280 mutation in MAP tau favors exon 10 skipping in vivoJohn C van Swieten, Iraad F Bronner, Asma Azmani, et al.
Brain : a Journal of Neurology|July 15, 2005
Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathologyI F Bronner, B C ter Meulen, A Azmani, et al.
Genome Research|May 20, 2016
Quantitative insertion-site sequencing (QIseq) for high throughput phenotyping of transposon mutantsIraad F Bronner, Thomas D Otto, Min Zhang, et al.
Pageof 8