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Peter Meinke

Showing results (11-20 of 51) with videos related to

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The Journal of Allergy and Clinical Immunology. in Practice|May 16, 2025
Hypertension risk in patients having hereditary angioedema with plasminogen gene mutation K330EKonrad Bork, Karin Wulff, Peter Meinke, et al.
Methods in Enzymology|January 19, 2016
Purification of Lamins and Soluble Fragments of NETsAlexandr A Makarov, Andrea Rizzotto, Peter Meinke, et al.
Journal of Neurology|June 14, 2026
Current biomarker development in myotonic dystrophiesMalin Larsen, Daniel H Mendelsohn, Felix Kleefeld, et al.
Clinical Immunology (Orlando, Fla.)|August 19, 2011
A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitorKonrad Bork, Karin Wulff, Peter Meinke, et al.
The Journal of Allergy and Clinical Immunology. in Practice|February 14, 2023
Gene Mutations Linked to Hereditary Angioedema in Solitary Angioedema Patients With Normal C1 InhibitorKonrad Bork, Karin Wulff, Günther Witzke, et al.
Human Mutation|December 31, 2013
Contribution of SUN1 mutations to the pathomechanism in muscular dystrophiesPing Li, Peter Meinke, Le Thi Thanh Huong, et al.
Scientific Reports|June 11, 2024
Author Correction: Degeneration of muscle spindles in a murine model of Pompe diseaseBridgette Watkins, Jürgen Schultheiß, Andi Rafuna, et al.
International Journal of Molecular Sciences|August 27, 2021
Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1Vanessa Todorow, Stefan Hintze, Alastair R W Kerr, et al.
Scientific Reports|April 21, 2023
Degeneration of muscle spindles in a murine model of Pompe diseaseBridgette Watkins, Jürgen Schultheiß, Andi Rafuna, et al.
Life (Basel, Switzerland)|October 27, 2022
Isolation and Characterization of Primary DMD Pig Muscle Cells as an <i>In Vitro</i> Model for Preclinical Research on Duchenne Muscular DystrophyTina Donandt, Stefan Hintze, Sabine Krause, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
The Journal of Allergy and Clinical Immunology. in Practice|May 16, 2025
Hypertension risk in patients having hereditary angioedema with plasminogen gene mutation K330EKonrad Bork, Karin Wulff, Peter Meinke, et al.
Methods in Enzymology|January 19, 2016
Purification of Lamins and Soluble Fragments of NETsAlexandr A Makarov, Andrea Rizzotto, Peter Meinke, et al.
Journal of Neurology|June 14, 2026
Current biomarker development in myotonic dystrophiesMalin Larsen, Daniel H Mendelsohn, Felix Kleefeld, et al.
Clinical Immunology (Orlando, Fla.)|August 19, 2011
A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitorKonrad Bork, Karin Wulff, Peter Meinke, et al.
The Journal of Allergy and Clinical Immunology. in Practice|February 14, 2023
Gene Mutations Linked to Hereditary Angioedema in Solitary Angioedema Patients With Normal C1 InhibitorKonrad Bork, Karin Wulff, Günther Witzke, et al.
Human Mutation|December 31, 2013
Contribution of SUN1 mutations to the pathomechanism in muscular dystrophiesPing Li, Peter Meinke, Le Thi Thanh Huong, et al.
Scientific Reports|June 11, 2024
Author Correction: Degeneration of muscle spindles in a murine model of Pompe diseaseBridgette Watkins, Jürgen Schultheiß, Andi Rafuna, et al.
International Journal of Molecular Sciences|August 27, 2021
Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1Vanessa Todorow, Stefan Hintze, Alastair R W Kerr, et al.
Scientific Reports|April 21, 2023
Degeneration of muscle spindles in a murine model of Pompe diseaseBridgette Watkins, Jürgen Schultheiß, Andi Rafuna, et al.
Life (Basel, Switzerland)|October 27, 2022
Isolation and Characterization of Primary DMD Pig Muscle Cells as an <i>In Vitro</i> Model for Preclinical Research on Duchenne Muscular DystrophyTina Donandt, Stefan Hintze, Sabine Krause, et al.
Pageof 6