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The goal of the project is to identify interactors of GRASP, a golgi-associated protein, to elucidate the mechanism of unconventional secretion.
ORGANISM(S): Homo sapiens (Human) 
2021-10-02 | PXD014247 | Pride
The 22q11.2 deletion syndrome (22q11.2DS) is the most common copy number variant (CNV)-associated syndrome, leading to congenital and neuropsychiatric anomalies. Patient-derived, induced pluripotent stem cell (iPS) models have provided important insight into the mechanisms of phenotypic features of ...
ORGANISM(S): Homo sapiens (Human) 
2023-05-11 | PXD032075 | Pride
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