Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Matthias Vorgerd

Showing results (51-60 of 140) with videos related to

Pageof 14
Sort By:
Muscle & Nerve|October 24, 2019
Chaperones in sporadic inclusion body myositis-Validation of proteomic dataAnne-Katrin Güttsches, Frank Jacobsen, Anja Schreiner, et al.
Acta Neuropathologica|October 31, 2012
Filamin C-related myopathies: pathology and mechanismsDieter O Fürst, Lev G Goldfarb, Rudolf A Kley, et al.
Molecules (Basel, Switzerland)|November 9, 2024
Ion Mobility QTOF-MS Untargeted Lipidomics of Human Serum Reveals a Metabolic Fingerprint for GNE MyopathyCristina Manis, Mattia Casula, Andreas Roos, et al.
Muscle & Nerve|May 27, 2003
Breakdown of adenine nucleotide pool in fatiguing skeletal muscle in McArdle's disease: a noninvasive 31P-MRS and EMG studyJochen Zange, Torsten Grehl, Catherine Disselhorst-Klug, et al.
Human Molecular Genetics|April 1, 2005
Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitroHarald Bär, Dirk Fischer, Bertrand Goudeau, et al.
Human Molecular Genetics|April 7, 2007
The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathyThomas Löwe, Rudolf A Kley, Peter F M van der Ven, et al.
NMR in Biomedicine|February 1, 2022
Robustness and stability of volume-based tractography in a multicenter settingJohannes Forsting, Robert Rehmann, Marlena Rohm, et al.
NMR in Biomedicine|July 10, 2024
Prospective longitudinal cohort study of quantitative muscle magnetic resonance imaging in a healthy control populationJohannes Forsting, Robert Rehmann, Marlena Rohm, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2005
Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's diseaseCarsten Saft, Jochen Zange, Jürgen Andrich, et al.
Autophagy|December 15, 2012
Impairment of protein degradation in myofibrillar myopathy caused by FLNC/filamin C mutationsRudolf A Kley, Peter F M van der Ven, Montse Olivé, et al.
Pageof 14

Showing results (51-60 of 140) with videos related to

Sort By:
Pageof 14
Muscle & Nerve|October 24, 2019
Chaperones in sporadic inclusion body myositis-Validation of proteomic dataAnne-Katrin Güttsches, Frank Jacobsen, Anja Schreiner, et al.
Acta Neuropathologica|October 31, 2012
Filamin C-related myopathies: pathology and mechanismsDieter O Fürst, Lev G Goldfarb, Rudolf A Kley, et al.
Molecules (Basel, Switzerland)|November 9, 2024
Ion Mobility QTOF-MS Untargeted Lipidomics of Human Serum Reveals a Metabolic Fingerprint for GNE MyopathyCristina Manis, Mattia Casula, Andreas Roos, et al.
Muscle & Nerve|May 27, 2003
Breakdown of adenine nucleotide pool in fatiguing skeletal muscle in McArdle's disease: a noninvasive 31P-MRS and EMG studyJochen Zange, Torsten Grehl, Catherine Disselhorst-Klug, et al.
Human Molecular Genetics|April 1, 2005
Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitroHarald Bär, Dirk Fischer, Bertrand Goudeau, et al.
Human Molecular Genetics|April 7, 2007
The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathyThomas Löwe, Rudolf A Kley, Peter F M van der Ven, et al.
NMR in Biomedicine|February 1, 2022
Robustness and stability of volume-based tractography in a multicenter settingJohannes Forsting, Robert Rehmann, Marlena Rohm, et al.
NMR in Biomedicine|July 10, 2024
Prospective longitudinal cohort study of quantitative muscle magnetic resonance imaging in a healthy control populationJohannes Forsting, Robert Rehmann, Marlena Rohm, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2005
Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's diseaseCarsten Saft, Jochen Zange, Jürgen Andrich, et al.
Autophagy|December 15, 2012
Impairment of protein degradation in myofibrillar myopathy caused by FLNC/filamin C mutationsRudolf A Kley, Peter F M van der Ven, Montse Olivé, et al.
Pageof 14