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Sandra Jansen

Showing results (21-30 of 62) with videos related to

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American Journal of Medical Genetics. Part A|October 20, 2017
Biallelicframeshift mutation in RIN2 in a patient with intellectual disability and cataract, without RIN2 syndromeClaudia J M van Amen-Hellebrekers, Sandra Jansen, Alexander P A Stegmann, et al.
BMC Genomics|July 6, 2013
Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverageSandra Jansen, Bernhard Aigner, Hubert Pausch, et al.
Journal of Neuroinflammation|February 9, 2011
The formyl peptide receptor like-1 and scavenger receptor MARCO are involved in glial cell activation in bacterial meningitisBenedikt J Braun, Alexander Slowik, Stephen L Leib, et al.
The Journal of Clinical Investigation|March 11, 2009
Membrane-anchored uPAR regulates the proliferation, marrow pool size, engraftment, and mobilization of mouse hematopoietic stem/progenitor cellsMarc Tjwa, Nicolai Sidenius, Rute Moura, et al.
European Journal of Medical Genetics|June 15, 2016
Duplications of SLC1A3: Associated with ADHD and autismClaudia J M van Amen-Hellebrekers, Sandra Jansen, Rolph Pfundt, et al.
Annals of Surgery|August 3, 2020
The Effect of Arterial Disease Level on Outcomes of Supervised Exercise Therapy for Intermittent Claudication: A Prospective Cohort StudyMarijn M L van den Houten, Sandra Jansen, Lijckle van der Laan, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2009
Loss of the cholesterol-binding protein prominin-1/CD133 causes disk dysmorphogenesis and photoreceptor degenerationSerena Zacchigna, Hideyasu Oh, Michaela Wilsch-Bräuninger, et al.
BMC Genomics|November 2, 2014
Evaluation of variant identification methods for whole genome sequencing data in dairy cattleChristine F Baes, Marlies A Dolezal, James E Koltes, et al.
European Journal of Human Genetics : EJHG|July 12, 2020
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disordersIlse M van der Werf, Sandra Jansen, Petra F de Vries, et al.
Pageof 7

Showing results (21-30 of 62) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|October 20, 2017
Biallelicframeshift mutation in RIN2 in a patient with intellectual disability and cataract, without RIN2 syndromeClaudia J M van Amen-Hellebrekers, Sandra Jansen, Alexander P A Stegmann, et al.
BMC Genomics|July 6, 2013
Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverageSandra Jansen, Bernhard Aigner, Hubert Pausch, et al.
Journal of Neuroinflammation|February 9, 2011
The formyl peptide receptor like-1 and scavenger receptor MARCO are involved in glial cell activation in bacterial meningitisBenedikt J Braun, Alexander Slowik, Stephen L Leib, et al.
The Journal of Clinical Investigation|March 11, 2009
Membrane-anchored uPAR regulates the proliferation, marrow pool size, engraftment, and mobilization of mouse hematopoietic stem/progenitor cellsMarc Tjwa, Nicolai Sidenius, Rute Moura, et al.
European Journal of Medical Genetics|June 15, 2016
Duplications of SLC1A3: Associated with ADHD and autismClaudia J M van Amen-Hellebrekers, Sandra Jansen, Rolph Pfundt, et al.
Annals of Surgery|August 3, 2020
The Effect of Arterial Disease Level on Outcomes of Supervised Exercise Therapy for Intermittent Claudication: A Prospective Cohort StudyMarijn M L van den Houten, Sandra Jansen, Lijckle van der Laan, et al.
Developmental Medicine and Child Neurology|July 11, 2021
Genetic convergence of developmental and epileptic encephalopathies and intellectual disabilityGemma L Carvill, Sandra Jansen, Amy Lacroix, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2009
Loss of the cholesterol-binding protein prominin-1/CD133 causes disk dysmorphogenesis and photoreceptor degenerationSerena Zacchigna, Hideyasu Oh, Michaela Wilsch-Bräuninger, et al.
BMC Genomics|November 2, 2014
Evaluation of variant identification methods for whole genome sequencing data in dairy cattleChristine F Baes, Marlies A Dolezal, James E Koltes, et al.
European Journal of Human Genetics : EJHG|July 12, 2020
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disordersIlse M van der Werf, Sandra Jansen, Petra F de Vries, et al.
Pageof 7