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Rick Kamps

Showing results (11-20 of 25) with videos related to

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The American Journal of Pathology|November 5, 2010
Olfactomedin-4 regulation by estrogen in the human endometrium requires epidermal growth factor signalingHellen Dassen, Chamindie Punyadeera, Bert Delvoux, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 27, 2017
Human embryonic stem cell-derived cardiomyocytes as an in vitro model to study cardiac insulin resistanceIlvy M E Geraets, Dipanjan Chanda, Florence H J van Tienen, et al.
Oncotarget|October 31, 2015
Germ-line variants identified by next generation sequencing in a panel of estrogen and cancer associated genes correlate with poor clinical outcome in Lynch syndrome patientsBalazs Jóri, Rick Kamps, Sofia Xanthoulea, et al.
Genetics|October 26, 2016
Replication Errors Made During Oogenesis Lead to Detectable De Novo mtDNA Mutations in Zebrafish Oocytes with a Low mtDNA Copy NumberAuke B C Otten, Alphons P M Stassen, Michiel Adriaens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 10, 2010
Rapid, high sensitivity, point-of-care test for cardiac troponin based on optomagnetic biosensorWendy U Dittmer, Toon H Evers, Willie M Hardeman, et al.
Brain : a Journal of Neurology|February 21, 2013
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndromeMike Gerards, Rick Kamps, Jo van Oevelen, et al.
Endocrinology|July 21, 2007
Role and regulation of the serum- and glucocorticoid-regulated kinase 1 in fertile and infertile human endometriumFakhera Feroze-Zaidi, Luca Fusi, Masashi Takano, et al.
Frontiers in Molecular Neuroscience|November 3, 2017
Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I DefectTom E J Theunissen, Mike Gerards, Debby M E I Hellebrekers, et al.
The Journal of Pediatrics|January 14, 2017
Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome SequencingTom E J Theunissen, Suzanne C E H Sallevelt, Debby M E I Hellebrekers, et al.
European Journal of Human Genetics : EJHG|February 15, 2018
Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain diseaseRick Kamps, Radek Szklarczyk, Tom E Theunissen, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
The American Journal of Pathology|November 5, 2010
Olfactomedin-4 regulation by estrogen in the human endometrium requires epidermal growth factor signalingHellen Dassen, Chamindie Punyadeera, Bert Delvoux, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 27, 2017
Human embryonic stem cell-derived cardiomyocytes as an in vitro model to study cardiac insulin resistanceIlvy M E Geraets, Dipanjan Chanda, Florence H J van Tienen, et al.
Oncotarget|October 31, 2015
Germ-line variants identified by next generation sequencing in a panel of estrogen and cancer associated genes correlate with poor clinical outcome in Lynch syndrome patientsBalazs Jóri, Rick Kamps, Sofia Xanthoulea, et al.
Genetics|October 26, 2016
Replication Errors Made During Oogenesis Lead to Detectable De Novo mtDNA Mutations in Zebrafish Oocytes with a Low mtDNA Copy NumberAuke B C Otten, Alphons P M Stassen, Michiel Adriaens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 10, 2010
Rapid, high sensitivity, point-of-care test for cardiac troponin based on optomagnetic biosensorWendy U Dittmer, Toon H Evers, Willie M Hardeman, et al.
Brain : a Journal of Neurology|February 21, 2013
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndromeMike Gerards, Rick Kamps, Jo van Oevelen, et al.
Endocrinology|July 21, 2007
Role and regulation of the serum- and glucocorticoid-regulated kinase 1 in fertile and infertile human endometriumFakhera Feroze-Zaidi, Luca Fusi, Masashi Takano, et al.
Frontiers in Molecular Neuroscience|November 3, 2017
Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I DefectTom E J Theunissen, Mike Gerards, Debby M E I Hellebrekers, et al.
The Journal of Pediatrics|January 14, 2017
Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome SequencingTom E J Theunissen, Suzanne C E H Sallevelt, Debby M E I Hellebrekers, et al.
European Journal of Human Genetics : EJHG|February 15, 2018
Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain diseaseRick Kamps, Radek Szklarczyk, Tom E Theunissen, et al.
Pageof 3