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J Boon

Showing results (281-290 of 292) with videos related to

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 13, 2018
Indications for neuromuscular ultrasound: Expert opinion and review of the literatureFrancis O Walker, Michael S Cartwright, Katharine E Alter, et al.
Science (New York, N.Y.)|May 16, 2024
DNA damage induces p53-independent apoptosis through ribosome stallingNicolaas J Boon, Rafaela A Oliveira, Pierré-René Körner, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 30, 2006
[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities]E M A Boormans, J M M van Lith, C M Bilardo, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|April 30, 2015
APOE ɛ2 is associated with white matter hyperintensity volume in CADASILBenno Gesierich, Christian Opherk, Jonathan Rosand, et al.
Stroke|March 1, 2014
Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASILChristian Opherk, Mariya Gonik, Marco Duering, et al.
Prenatal Diagnosis|October 18, 2016
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impactDick Oepkes, G C Lieve Page-Christiaens, Caroline J Bax, et al.
American Journal of Medical Genetics. Part A|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorderCaroline Dias, Rolph Pfundt, Tjitske Kleefstra, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 8, 2022
Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up StudyCatharina J Heesterbeek, Sietse M Aukema, Robert-Jan H Galjaard, et al.
NPJ Genomic Medicine|November 25, 2021
Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodMichael A Levy, David B Beck, Kay Metcalfe, et al.
NPJ Genomic Medicine|November 9, 2021
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodMichael A Levy, David B Beck, Kay Metcalfe, et al.
Pageof 30

Showing results (281-290 of 292) with videos related to

Sort By:
Pageof 30
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 13, 2018
Indications for neuromuscular ultrasound: Expert opinion and review of the literatureFrancis O Walker, Michael S Cartwright, Katharine E Alter, et al.
Science (New York, N.Y.)|May 16, 2024
DNA damage induces p53-independent apoptosis through ribosome stallingNicolaas J Boon, Rafaela A Oliveira, Pierré-René Körner, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 30, 2006
[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities]E M A Boormans, J M M van Lith, C M Bilardo, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|April 30, 2015
APOE ɛ2 is associated with white matter hyperintensity volume in CADASILBenno Gesierich, Christian Opherk, Jonathan Rosand, et al.
Stroke|March 1, 2014
Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASILChristian Opherk, Mariya Gonik, Marco Duering, et al.
Prenatal Diagnosis|October 18, 2016
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impactDick Oepkes, G C Lieve Page-Christiaens, Caroline J Bax, et al.
American Journal of Medical Genetics. Part A|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorderCaroline Dias, Rolph Pfundt, Tjitske Kleefstra, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 8, 2022
Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up StudyCatharina J Heesterbeek, Sietse M Aukema, Robert-Jan H Galjaard, et al.
NPJ Genomic Medicine|November 25, 2021
Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodMichael A Levy, David B Beck, Kay Metcalfe, et al.
NPJ Genomic Medicine|November 9, 2021
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodMichael A Levy, David B Beck, Kay Metcalfe, et al.
Pageof 30