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ProteomicsProtein signature of human skin fibroblasts indicates the suitability to serve as in vitro model for neuromuscular diseases (AAAS-Data)
The elucidation of pathomechanisms leading to the manifestation of neuromuscular diseases (NMDs) represents an important step toward the understanding of the genesis of the respective disease and might help to define starting points for (new) therapeutic intervention concepts. However, these “discov...
ORGANISM(S): Homo sapiens (Human) 
2020-11-10 | PXD019201 | Pride
Allgrove syndrome Aladin Aaas Myopodin/synaptopodin-2 Triple-a syndrome Ataxin-2 
ProteomicsProtein signature of human skin fibroblasts indicates the suitability to serve as in vitro model for neuromuscular diseases (Library Data)
The elucidation of pathomechanisms leading to the manifestation of neuromuscular diseases (NMDs) represents an important step toward the understanding of the genesis of the respective disease and might help to define starting points for (new) therapeutic intervention concepts. However, these “discov...
ORGANISM(S): Homo sapiens (Human) 
2020-11-10 | PXD019060 | Pride
Allgrove syndrome Aladin Aaas Myopodin/synaptopodin-2 Triple-a syndrome Ataxin-2 
TranscriptomicsTranscription profiling of mouse SNF5 liver-specific inactivation in SNF5 flox/knockouts
Effect of liver-specific inactivation of SNF5 on liver transcriptome. Comparison of control and mutant livers.
ORGANISM(S): Mus musculus 
2005-12-19 | E-MEXP-241 | biostudies-arrayexpress
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