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P RICHARD

Showing results (891-900 of 939) with videos related to

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Resuscitation|December 24, 2013
Implementation trial of the basic life support termination of resuscitation rule: reducing the transport of futile out-of-hospital cardiac arrestsLaurie J Morrison, Don Eby, Precilla V Veigas, et al.
Physical Review Letters|January 24, 2015
Correlation-induced self-doping in the iron-pnictide superconductor Ba2Ti2Fe2As4OJ-Z Ma, A van Roekeghem, P Richard, et al.
Science Advances|May 7, 2019
Dirac nodal surfaces and nodal lines in ZrSiSB-B Fu, C-J Yi, T-T Zhang, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|January 18, 2019
A systematic, deep sequencing-based methodology for identification of mixed-genotype hepatitis C virus infectionsAndrea D Olmstead, Vincent Montoya, Celia K Chui, et al.
British Journal of Cancer|May 14, 2009
Organ-specific inhibition of metastatic colon carcinoma by CXCR3 antagonismB Cambien, B F Karimdjee, P Richard-Fiardo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Physical Review Letters|December 5, 2015
Observation of Fermi-Arc Spin Texture in TaAsB Q Lv, S Muff, T Qian, et al.
Brain Communications|November 29, 2023
Dorsal subthalamic nucleus targeting in deep brain stimulation: microelectrode recording versus 7-Tesla connectivityNaomi I Kremer, Mark J Roberts, Wouter V Potters, et al.
Journal of Medical Genetics|April 16, 1998
PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophyP Guicheney, N Vignier, X Zhang, et al.
Diabetes & Metabolism|October 6, 2018
Cardiometabolic assessment of lamin A/C gene mutation carriers: a phenotype-genotype correlationM Kwapich, D Lacroix, S Espiard, et al.
Pageof 94

Showing results (891-900 of 939) with videos related to

Sort By:
Pageof 94
Resuscitation|December 24, 2013
Implementation trial of the basic life support termination of resuscitation rule: reducing the transport of futile out-of-hospital cardiac arrestsLaurie J Morrison, Don Eby, Precilla V Veigas, et al.
Physical Review Letters|January 24, 2015
Correlation-induced self-doping in the iron-pnictide superconductor Ba2Ti2Fe2As4OJ-Z Ma, A van Roekeghem, P Richard, et al.
Science Advances|May 7, 2019
Dirac nodal surfaces and nodal lines in ZrSiSB-B Fu, C-J Yi, T-T Zhang, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|January 18, 2019
A systematic, deep sequencing-based methodology for identification of mixed-genotype hepatitis C virus infectionsAndrea D Olmstead, Vincent Montoya, Celia K Chui, et al.
British Journal of Cancer|May 14, 2009
Organ-specific inhibition of metastatic colon carcinoma by CXCR3 antagonismB Cambien, B F Karimdjee, P Richard-Fiardo, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Physical Review Letters|December 5, 2015
Observation of Fermi-Arc Spin Texture in TaAsB Q Lv, S Muff, T Qian, et al.
Brain Communications|November 29, 2023
Dorsal subthalamic nucleus targeting in deep brain stimulation: microelectrode recording versus 7-Tesla connectivityNaomi I Kremer, Mark J Roberts, Wouter V Potters, et al.
Journal of Medical Genetics|April 16, 1998
PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophyP Guicheney, N Vignier, X Zhang, et al.
Diabetes & Metabolism|October 6, 2018
Cardiometabolic assessment of lamin A/C gene mutation carriers: a phenotype-genotype correlationM Kwapich, D Lacroix, S Espiard, et al.
Pageof 94