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Showing results (1351-1360 of 1,983) with videos related to

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AJR. American Journal of Roentgenology|May 23, 2006
Clinical value of MDCT in the diagnosis of coronary artery disease in patients with a low pretest likelihood of significant diseaseKonstantin Nikolaou, Carsten Rist, Bernd J Wintersperger, et al.
Cell Death and Differentiation|January 16, 2007
Cyclin-dependent kinase 5 is an upstream regulator of mitochondrial fission during neuronal apoptosisK Meuer, I E Suppanz, P Lingor, et al.
Epilepsia|June 8, 2007
Severe epilepsy in X-linked creatine transporter defect (CRTR-D)Maria Margherita Mancardi, Ubaldo Caruso, Maria Cristina Schiaffino, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 24, 2010
New fluorinated rhodamines for optical microscopy and nanoscopyGyuzel Yu Mitronova, Vladimir N Belov, Mariano L Bossi, et al.
Molecular Genetics and Metabolism|October 25, 2011
Evaluation of two year treatment outcome and limited impact of arginine restriction in a patient with GAMT deficiencySaadet Mercimek-Mahmutoglu, Mary Dunbar, Andrea Friesen, et al.
Atherosclerosis|April 10, 2012
Asymmetric dimethylarginine in adults with cystathionine β-synthase deficiencyMonica S Rocha, Tom Teerlink, Mirian C H Janssen, et al.
Oxidative Medicine and Cellular Longevity|July 9, 2019
High Concentration of Low-Density Lipoprotein Results in Disturbances in Mitochondrial Transcription and Functionality in Endothelial CellsStefanie Gonnissen, Johannes Ptok, Christine Goy, et al.
Cardiovascular and Interventional Radiology|May 20, 2015
Safety of Radioembolization with (90)Yttrium Resin Microspheres Depending on Coiling or No-Coiling of Aberrant/High-Risk VesselsP M Paprottka, K J Paprottka, A Walter, et al.
Nature Genetics|November 5, 1997
Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase geneG A Jansen, R Ofman, S Ferdinandusse, et al.
Journal of Internal Medicine|January 5, 2000
Hyperhomocysteinaemia is not related to risk of distal somatic polyneuropathy: the Hoorn StudyE K Hoogeveen, P J Kostense, G D Valk, et al.
Pageof 199

Showing results (1351-1360 of 1,983) with videos related to

Sort By:
Pageof 199
AJR. American Journal of Roentgenology|May 23, 2006
Clinical value of MDCT in the diagnosis of coronary artery disease in patients with a low pretest likelihood of significant diseaseKonstantin Nikolaou, Carsten Rist, Bernd J Wintersperger, et al.
Cell Death and Differentiation|January 16, 2007
Cyclin-dependent kinase 5 is an upstream regulator of mitochondrial fission during neuronal apoptosisK Meuer, I E Suppanz, P Lingor, et al.
Epilepsia|June 8, 2007
Severe epilepsy in X-linked creatine transporter defect (CRTR-D)Maria Margherita Mancardi, Ubaldo Caruso, Maria Cristina Schiaffino, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 24, 2010
New fluorinated rhodamines for optical microscopy and nanoscopyGyuzel Yu Mitronova, Vladimir N Belov, Mariano L Bossi, et al.
Molecular Genetics and Metabolism|October 25, 2011
Evaluation of two year treatment outcome and limited impact of arginine restriction in a patient with GAMT deficiencySaadet Mercimek-Mahmutoglu, Mary Dunbar, Andrea Friesen, et al.
Atherosclerosis|April 10, 2012
Asymmetric dimethylarginine in adults with cystathionine β-synthase deficiencyMonica S Rocha, Tom Teerlink, Mirian C H Janssen, et al.
Oxidative Medicine and Cellular Longevity|July 9, 2019
High Concentration of Low-Density Lipoprotein Results in Disturbances in Mitochondrial Transcription and Functionality in Endothelial CellsStefanie Gonnissen, Johannes Ptok, Christine Goy, et al.
Cardiovascular and Interventional Radiology|May 20, 2015
Safety of Radioembolization with (90)Yttrium Resin Microspheres Depending on Coiling or No-Coiling of Aberrant/High-Risk VesselsP M Paprottka, K J Paprottka, A Walter, et al.
Nature Genetics|November 5, 1997
Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase geneG A Jansen, R Ofman, S Ferdinandusse, et al.
Journal of Internal Medicine|January 5, 2000
Hyperhomocysteinaemia is not related to risk of distal somatic polyneuropathy: the Hoorn StudyE K Hoogeveen, P J Kostense, G D Valk, et al.
Pageof 199