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Unknown
(47)
Proteomics
(3)
Transcriptomics
(1)
Organisms
Homo sapiens
(2)
Mus musculus
(1)
Rattus norvegicus
(1)
Repository
pride
(2)
biostudies-arrayexpress
(1)
jPOST
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Diaphragm
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Muscle stem cell
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Mass Spectrometry
(2)
Shotgun proteomics
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2014
(1)
2022
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2024
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2020
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Transcription profiling by array
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2022
(9)
2020
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Lab affiliation
Department of Surgery, Charité Universitätsmedizin Berlin
(1)
Marcus Krüger Lab, CECAD, University of Cologne, Germany
(1)
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Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1).
Not available
S-EPMC3760810
|
biostudies-literature
Cite
World's fastest brain-computer interface: Combining EEG2Code with deep learning.
Not available
S-EPMC6730910
|
biostudies-literature
Cite
Modelling the brain response to arbitrary visual stimulation patterns for a flexible high-speed Brain-Computer Interface.
Not available
S-EPMC6197660
|
biostudies-literature
Cite
Human satellite cells have regenerative capacity and are genetically manipulable.
Not available
S-EPMC4191042
|
biostudies-literature
Cite
Nerve damage induced skeletal muscle atrophy is associated with increased accumulation of intramuscular glucose and polyol pathway intermediates.
Not available
S-EPMC7002415
|
biostudies-literature
Cite
Full-length Dysferlin Transfer by the Hyperactive Sleeping Beauty Transposase Restores Dysferlin-deficient Muscle.
Not available
S-EPMC5012550
|
biostudies-literature
Cite
mRNA-mediated delivery of gene editing tools to human primary muscle stem cells.
Not available
S-EPMC8931293
|
biostudies-literature
Cite
Generation of hiPSC-Derived Skeletal Muscle Cells: Exploiting the Potential of Skeletal Muscle-Derived hiPSCs.
Not available
S-EPMC9138862
|
biostudies-literature
Cite
LMNA
Co-Regulated Gene Expression as a Suitable Readout after Precise Gene Correction.
Not available
S-EPMC9778678
|
biostudies-literature
Cite
Dysferlin-deficient immortalized human myoblasts and myotubes as a useful tool to study dysferlinopathy.
Not available
S-EPMC3274833
|
biostudies-literature
Cite
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