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Showing results (731-740 of 778) with videos related to

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Scientific Reports|February 27, 2015
Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fatKlaus Lehnert, Hamish Ward, Sarah D Berry, et al.
Molecules (Basel, Switzerland)|January 10, 2019
Cardiomyocyte Progenitor Cells as a Functional Gene Delivery Vehicle for Long-Term Biological PacingAnna M D Végh, A Dénise den Haan, Lucía Cócera Ortega, et al.
International Journal of Cancer|October 16, 2025
Olaparib for patients with tumors harboring alterations in homologous recombination repair genes: Results from the drug rediscovery protocolIlse A C Spiekman, Niven Mehra, Laurien J Zeverijn, et al.
Nature Communications|December 5, 2025
PITX2 dosage-dependent changes in pacemaker cell state underlie sinus node dysfunction and atrial arrhythmiasLieve E van der Maarel, M Ridwane Mungroo, Otto J Mulleners, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalusAnnemieke J M H Verkerk, Rachel Schot, Laura van Waterschoot, et al.
Archives of Disease in Childhood|February 4, 2019
Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasiaAnnelieke A A van der Linde, Yvonne Schönbeck, Hetty J van der Kamp, et al.
Journal of the American College of Cardiology|December 3, 2013
Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemiaRoos F J Marsman, Connie R Bezzina, Fabian Freiberg, et al.
Nature Genetics|August 3, 2010
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobinJoseph Borg, Petros Papadopoulos, Marianthi Georgitsi, et al.
Physics in Medicine and Biology|July 31, 2024
Robotic MR-guided high dose rate brachytherapy needle implantation in the prostate (ROBiNSon)-a proof-of-concept studyMarnix J A Rasing, Leonard J van Schelven, Astrid L H M W van Lier, et al.
European Journal of Cancer (Oxford, England : 1990)|March 14, 2026
BRAF<sup>V600E</sup>-mutated central nervous system tumors benefit from treatment with dabrafenib plus trametinib: Results from the Drug Rediscovery ProtocolSoemeya F Haj Mohammad, Ilse A C Spiekman, Karlijn Verkerk, et al.
Pageof 78

Showing results (731-740 of 778) with videos related to

Sort By:
Pageof 78
Scientific Reports|February 27, 2015
Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fatKlaus Lehnert, Hamish Ward, Sarah D Berry, et al.
Molecules (Basel, Switzerland)|January 10, 2019
Cardiomyocyte Progenitor Cells as a Functional Gene Delivery Vehicle for Long-Term Biological PacingAnna M D Végh, A Dénise den Haan, Lucía Cócera Ortega, et al.
International Journal of Cancer|October 16, 2025
Olaparib for patients with tumors harboring alterations in homologous recombination repair genes: Results from the drug rediscovery protocolIlse A C Spiekman, Niven Mehra, Laurien J Zeverijn, et al.
Nature Communications|December 5, 2025
PITX2 dosage-dependent changes in pacemaker cell state underlie sinus node dysfunction and atrial arrhythmiasLieve E van der Maarel, M Ridwane Mungroo, Otto J Mulleners, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalusAnnemieke J M H Verkerk, Rachel Schot, Laura van Waterschoot, et al.
Archives of Disease in Childhood|February 4, 2019
Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasiaAnnelieke A A van der Linde, Yvonne Schönbeck, Hetty J van der Kamp, et al.
Journal of the American College of Cardiology|December 3, 2013
Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemiaRoos F J Marsman, Connie R Bezzina, Fabian Freiberg, et al.
Nature Genetics|August 3, 2010
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobinJoseph Borg, Petros Papadopoulos, Marianthi Georgitsi, et al.
Physics in Medicine and Biology|July 31, 2024
Robotic MR-guided high dose rate brachytherapy needle implantation in the prostate (ROBiNSon)-a proof-of-concept studyMarnix J A Rasing, Leonard J van Schelven, Astrid L H M W van Lier, et al.
European Journal of Cancer (Oxford, England : 1990)|March 14, 2026
BRAF<sup>V600E</sup>-mutated central nervous system tumors benefit from treatment with dabrafenib plus trametinib: Results from the Drug Rediscovery ProtocolSoemeya F Haj Mohammad, Ilse A C Spiekman, Karlijn Verkerk, et al.
Pageof 78