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P Kramer
K Stern

Showing results (381-390 of 570) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|June 21, 2006
Cutting edge: impaired glycosphingolipid trafficking and NKT cell development in mice lacking Niemann-Pick type C1 proteinYuval Sagiv, Kelly Hudspeth, Jochen Mattner, et al.
The Journal of Biological Chemistry|June 23, 1998
Characterization of the cytoprotective action of peroxynitrite decomposition catalystsT P Misko, M K Highkin, A W Veenhuizen, et al.
BMC Medical Research Methodology|September 16, 2008
The HCV Synthesis Project: scope, methodology, and preliminary resultsRebecca K Stern, Holly Hagan, Corina Lelutiu-Weinberger, et al.
Journal of Biomedical Materials Research|February 19, 1998
Piezoelectric response of scleral collagenS Ghosh, B Z Mei, V Lubkin, et al.
Nature Genetics|February 1, 1995
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder populationN Risch, D de Leon, L Ozelius, et al.
Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|February 20, 2016
Pigment Degradation in Oil Paint Induced by Indoor Climate: Comparison of Visual and Computational Backscattered Electron ImagesKatrien Keune, Rick P Kramer, Zara Huijbregts, et al.
The International Journal of Artificial Organs|July 1, 1980
Management of anuric intensive-care patients with arteriovenous hemofiltrationP Kramer, G Kaufhold, H J Gröne, et al.
Journal of Cardiothoracic and Vascular Anesthesia|May 4, 2005
Intraoperative glucose control in diabetic and nondiabetic patients during cardiac surgeryCharles E Smith, Nicholas R Styn, Satish Kalhan, et al.
Hospital Pediatrics|March 22, 2023
Improving the Rate of Delayed Cord Clamping in Preterm Infants: A Quality Improvement ProjectShannon Chan, Meghan Duck, Kate Frometa, et al.
Human Molecular Genetics|May 1, 1997
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2M Litt, R Carrero-Valenzuela, D M LaMorticella, et al.
Pageof 57

Showing results (381-390 of 570) with videos related to

Sort By:
Pageof 57
Journal of Immunology (Baltimore, Md. : 1950)|June 21, 2006
Cutting edge: impaired glycosphingolipid trafficking and NKT cell development in mice lacking Niemann-Pick type C1 proteinYuval Sagiv, Kelly Hudspeth, Jochen Mattner, et al.
The Journal of Biological Chemistry|June 23, 1998
Characterization of the cytoprotective action of peroxynitrite decomposition catalystsT P Misko, M K Highkin, A W Veenhuizen, et al.
BMC Medical Research Methodology|September 16, 2008
The HCV Synthesis Project: scope, methodology, and preliminary resultsRebecca K Stern, Holly Hagan, Corina Lelutiu-Weinberger, et al.
Journal of Biomedical Materials Research|February 19, 1998
Piezoelectric response of scleral collagenS Ghosh, B Z Mei, V Lubkin, et al.
Nature Genetics|February 1, 1995
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder populationN Risch, D de Leon, L Ozelius, et al.
Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|February 20, 2016
Pigment Degradation in Oil Paint Induced by Indoor Climate: Comparison of Visual and Computational Backscattered Electron ImagesKatrien Keune, Rick P Kramer, Zara Huijbregts, et al.
The International Journal of Artificial Organs|July 1, 1980
Management of anuric intensive-care patients with arteriovenous hemofiltrationP Kramer, G Kaufhold, H J Gröne, et al.
Journal of Cardiothoracic and Vascular Anesthesia|May 4, 2005
Intraoperative glucose control in diabetic and nondiabetic patients during cardiac surgeryCharles E Smith, Nicholas R Styn, Satish Kalhan, et al.
Hospital Pediatrics|March 22, 2023
Improving the Rate of Delayed Cord Clamping in Preterm Infants: A Quality Improvement ProjectShannon Chan, Meghan Duck, Kate Frometa, et al.
Human Molecular Genetics|May 1, 1997
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2M Litt, R Carrero-Valenzuela, D M LaMorticella, et al.
Pageof 57