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Showing results (91-100 of 226) with videos related to

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NMR in Biomedicine|October 20, 2022
Ex vivo proton spectroscopy (<sup>1</sup> H-NMR) analysis of inborn errors of metabolism: Automatic and computer-assisted analysesClaire Cannet, Georg Frauendienst-Egger, Peter Freisinger, et al.
Journal of Translational Medicine|February 8, 2018
Immune monitoring and TCR sequencing of CD4 T cells in a long term responsive patient with metastasized pancreatic ductal carcinoma treated with individualized, neoepitope-derived multipeptide vaccines: a case reportKatja Sonntag, Hisayoshi Hashimoto, Matthias Eyrich, et al.
Neuromolecular Medicine|April 8, 2019
A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1CSaranya Suriyanarayanan, Alaa Othman, Bianca Dräger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 14, 2021
Novel CACNA1A Variant p.Cys256Phe Disrupts Disulfide Bonds and Causes Spinocerebellar AtaxiaYuliia V Nikonishyna, Nadine J Ortner, Teresa Kaserer, et al.
Scientific Reports|March 16, 2019
The Parkinson's disease-linked Leucine-rich repeat kinase 2 (LRRK2) is required for insulin-stimulated translocation of GLUT4Natalja Funk, Marita Munz, Thomas Ott, et al.
Neurobiology of Aging|November 16, 2017
Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypesCarlo Wilke, Jonathan Baets, Jan L De Bleecker, et al.
Plos One|April 2, 2015
No dopamine cell loss or changes in cytoskeleton function in transgenic mice expressing physiological levels of wild type or G2019S mutant LRRK2 and in human fibroblastsMarta Garcia-Miralles, Janaky Coomaraswamy, Karina Häbig, et al.
Journal of Inherited Metabolic Disease|June 27, 2021
3-Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency-A novel disorder of valine metabolismMelanie Meyer, Jana C Hollenbeck, Janine Reunert, et al.
Clinical Genetics|December 30, 2021
Di-genic inheritance of germline POLE and PMS2 pathogenic variants causes a unique condition associated with pediatric cancer predispositionOrli Michaeli, Hagay Ladany, Ayelet Erez, et al.
Journal of Neurogenetics|January 10, 2009
The Wuerzburg hybridoma library against Drosophila brainAlois Hofbauer, Thomas Ebel, Bernhard Waltenspiel, et al.
Pageof 23

Showing results (91-100 of 226) with videos related to

Sort By:
Pageof 23
NMR in Biomedicine|October 20, 2022
Ex vivo proton spectroscopy (<sup>1</sup> H-NMR) analysis of inborn errors of metabolism: Automatic and computer-assisted analysesClaire Cannet, Georg Frauendienst-Egger, Peter Freisinger, et al.
Journal of Translational Medicine|February 8, 2018
Immune monitoring and TCR sequencing of CD4 T cells in a long term responsive patient with metastasized pancreatic ductal carcinoma treated with individualized, neoepitope-derived multipeptide vaccines: a case reportKatja Sonntag, Hisayoshi Hashimoto, Matthias Eyrich, et al.
Neuromolecular Medicine|April 8, 2019
A Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1CSaranya Suriyanarayanan, Alaa Othman, Bianca Dräger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 14, 2021
Novel CACNA1A Variant p.Cys256Phe Disrupts Disulfide Bonds and Causes Spinocerebellar AtaxiaYuliia V Nikonishyna, Nadine J Ortner, Teresa Kaserer, et al.
Scientific Reports|March 16, 2019
The Parkinson's disease-linked Leucine-rich repeat kinase 2 (LRRK2) is required for insulin-stimulated translocation of GLUT4Natalja Funk, Marita Munz, Thomas Ott, et al.
Neurobiology of Aging|November 16, 2017
Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypesCarlo Wilke, Jonathan Baets, Jan L De Bleecker, et al.
Plos One|April 2, 2015
No dopamine cell loss or changes in cytoskeleton function in transgenic mice expressing physiological levels of wild type or G2019S mutant LRRK2 and in human fibroblastsMarta Garcia-Miralles, Janaky Coomaraswamy, Karina Häbig, et al.
Journal of Inherited Metabolic Disease|June 27, 2021
3-Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency-A novel disorder of valine metabolismMelanie Meyer, Jana C Hollenbeck, Janine Reunert, et al.
Clinical Genetics|December 30, 2021
Di-genic inheritance of germline POLE and PMS2 pathogenic variants causes a unique condition associated with pediatric cancer predispositionOrli Michaeli, Hagay Ladany, Ayelet Erez, et al.
Journal of Neurogenetics|January 10, 2009
The Wuerzburg hybridoma library against Drosophila brainAlois Hofbauer, Thomas Ebel, Bernhard Waltenspiel, et al.
Pageof 23