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Tobias Timmel
Markus Schuelke
Simone Spuler

Showing results (1-10 of 250) with videos related to

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Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|February 15, 2014
Identifying dynamic membrane structures with atomic-force microscopy and confocal imagingTobias Timmel, Markus Schuelke, Simone Spuler
American Journal of Physiology. Cell Physiology|April 24, 2015
Cavin 1 function does not follow caveolar morphologyTobias Timmel, Séverine Kunz, Franziska Seifert, et al.
Traffic (Copenhagen, Denmark)|June 12, 2012
Sarcolemmal repair is a slow process and includes EHD2Andreas Marg, Verena Schoewel, Tobias Timmel, et al.
Plos One|May 11, 2011
Region-specific expression of mitochondrial complex I genes during murine brain developmentStefanie Wirtz, Markus Schuelke
Nucleic Acids Research|June 7, 2012
HomozygosityMapper2012--bridging the gap between homozygosity mapping and deep sequencingDominik Seelow, Markus Schuelke
Plos Genetics|March 20, 2010
Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutationsAnna Rajab, Volker Straub, Liza J McCann, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 7, 2022
What is the Role of Thyroid Hormone Receptor Alpha 2 (TRα2) in Human Physiology?Sarah Paisdzior, Markus Schuelke, Heiko Krude
Journal of Inherited Metabolic Disease|February 4, 2015
Leukodystrophy with multiple beaded periventricular cysts: unusual cranial MRI results in Canavan diseaseAnne Drenckhahn, Markus Schuelke, Ellen Knierim
Stem Cell Research|September 13, 2024
Characterization of two iPSC lines from patients with maternally inherited leigh (MILS) and neuropathy, ataxia, and retinitis pigmentosa (NARP) syndrome carrying the MT-ATP6 m.8993 T>G mutation at different degrees of heteroplasmyAnna Maria Haschke, Sebastian Diecke, Markus Schuelke
Plos One|December 6, 2008
GeneDistiller--distilling candidate genes from linkage intervalsDominik Seelow, Jana Marie Schwarz, Markus Schuelke
Pageof 25

Showing results (1-10 of 250) with videos related to

Sort By:
Pageof 25
Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|February 15, 2014
Identifying dynamic membrane structures with atomic-force microscopy and confocal imagingTobias Timmel, Markus Schuelke, Simone Spuler
American Journal of Physiology. Cell Physiology|April 24, 2015
Cavin 1 function does not follow caveolar morphologyTobias Timmel, Séverine Kunz, Franziska Seifert, et al.
Traffic (Copenhagen, Denmark)|June 12, 2012
Sarcolemmal repair is a slow process and includes EHD2Andreas Marg, Verena Schoewel, Tobias Timmel, et al.
Plos One|May 11, 2011
Region-specific expression of mitochondrial complex I genes during murine brain developmentStefanie Wirtz, Markus Schuelke
Nucleic Acids Research|June 7, 2012
HomozygosityMapper2012--bridging the gap between homozygosity mapping and deep sequencingDominik Seelow, Markus Schuelke
Plos Genetics|March 20, 2010
Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutationsAnna Rajab, Volker Straub, Liza J McCann, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|March 7, 2022
What is the Role of Thyroid Hormone Receptor Alpha 2 (TRα2) in Human Physiology?Sarah Paisdzior, Markus Schuelke, Heiko Krude
Journal of Inherited Metabolic Disease|February 4, 2015
Leukodystrophy with multiple beaded periventricular cysts: unusual cranial MRI results in Canavan diseaseAnne Drenckhahn, Markus Schuelke, Ellen Knierim
Stem Cell Research|September 13, 2024
Characterization of two iPSC lines from patients with maternally inherited leigh (MILS) and neuropathy, ataxia, and retinitis pigmentosa (NARP) syndrome carrying the MT-ATP6 m.8993 T>G mutation at different degrees of heteroplasmyAnna Maria Haschke, Sebastian Diecke, Markus Schuelke
Plos One|December 6, 2008
GeneDistiller--distilling candidate genes from linkage intervalsDominik Seelow, Jana Marie Schwarz, Markus Schuelke
Pageof 25