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Andreas Ziegler

Showing results (291-300 of 422) with videos related to

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Psychiatric Genetics|June 10, 2014
Analysis of gastrin-releasing peptide gene and gastrin-releasing peptide receptor gene in patients with agoraphobiaKatrin Zimmermann, Heike Görgens, David Bräuer, et al.
Annals of Surgery|November 28, 2002
CDKN2A germline mutations in familial pancreatic cancerDetlef K Bartsch, Mercedes Sina-Frey, Sven Lang, et al.
Clinical Chemistry|July 13, 2021
Diagnostic Validation of a High-Sensitivity Cardiac Troponin I AssayNils A Sörensen, Alina Goßling, Johannes T Neumann, et al.
Clinical Science (London, England : 1979)|March 6, 2008
Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German populationPatrick Linsel-Nitschke, Anika Götz, Anja Medack, et al.
Psychiatric Genetics|February 26, 2009
Further evidence for DYX1C1 as a susceptibility factor for dyslexiaFaten Dahdouh, Heidi Anthoni, Isabel Tapia-Páez, et al.
The American Journal of Pathology|August 18, 2014
Nerve conduction velocity is regulated by the inositol polyphosphate-4-phosphatase II geneSusanne Lemcke, Susen Müller, Steffen Möller, et al.
Therapeutic Advances in Neurological Disorders|March 22, 2012
Incidence of therapy-related acute leukaemia in mitoxantrone-treated multiple sclerosis patients in GermanyAnke Stroet, Claudia Hemmelmann, Michaela Starck, et al.
The International Journal of Cardiovascular Imaging|October 9, 2025
Assessment of aortic and mitral valve regurgitation volumes by cardiovascular magnetic resonance in participants without valvular heart disease in the Hamburg City Health Study populationKatharina A Riedl, Georgios Koliopanos, Jan N Albrecht, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
No association between three xeroderma pigmentosum group C and one group G gene polymorphisms and risk of cutaneous melanomaSandra Blankenburg, Inke R König, Rotraut Moessner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 9, 2020
European ad-hoc consensus statement on gene replacement therapy for spinal muscular atrophyJanbernd Kirschner, Nina Butoianu, Nathalie Goemans, et al.
Pageof 43

Showing results (291-300 of 422) with videos related to

Sort By:
Pageof 43
Psychiatric Genetics|June 10, 2014
Analysis of gastrin-releasing peptide gene and gastrin-releasing peptide receptor gene in patients with agoraphobiaKatrin Zimmermann, Heike Görgens, David Bräuer, et al.
Annals of Surgery|November 28, 2002
CDKN2A germline mutations in familial pancreatic cancerDetlef K Bartsch, Mercedes Sina-Frey, Sven Lang, et al.
Clinical Chemistry|July 13, 2021
Diagnostic Validation of a High-Sensitivity Cardiac Troponin I AssayNils A Sörensen, Alina Goßling, Johannes T Neumann, et al.
Clinical Science (London, England : 1979)|March 6, 2008
Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German populationPatrick Linsel-Nitschke, Anika Götz, Anja Medack, et al.
Psychiatric Genetics|February 26, 2009
Further evidence for DYX1C1 as a susceptibility factor for dyslexiaFaten Dahdouh, Heidi Anthoni, Isabel Tapia-Páez, et al.
The American Journal of Pathology|August 18, 2014
Nerve conduction velocity is regulated by the inositol polyphosphate-4-phosphatase II geneSusanne Lemcke, Susen Müller, Steffen Möller, et al.
Therapeutic Advances in Neurological Disorders|March 22, 2012
Incidence of therapy-related acute leukaemia in mitoxantrone-treated multiple sclerosis patients in GermanyAnke Stroet, Claudia Hemmelmann, Michaela Starck, et al.
The International Journal of Cardiovascular Imaging|October 9, 2025
Assessment of aortic and mitral valve regurgitation volumes by cardiovascular magnetic resonance in participants without valvular heart disease in the Hamburg City Health Study populationKatharina A Riedl, Georgios Koliopanos, Jan N Albrecht, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
No association between three xeroderma pigmentosum group C and one group G gene polymorphisms and risk of cutaneous melanomaSandra Blankenburg, Inke R König, Rotraut Moessner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 9, 2020
European ad-hoc consensus statement on gene replacement therapy for spinal muscular atrophyJanbernd Kirschner, Nina Butoianu, Nathalie Goemans, et al.
Pageof 43