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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
High resolution mass spectrometry is used to confirm conjugation of fluorogenic nonstandard amino acids onto an intermediate molecule, and further verify site-specific ribosomal incorporation into different positions of a polypeptide.
ORGANISM(S): Escherichia coli 
2024-10-17 | PXD053593 | Pride
Comparison of three populations of OECs derived from the ONL of rats. The three populations were cultured employing the same culture medium but were maintained in vitro for a different amount of time (number of population doublings or PDs). OEC Ep cells were maintained for less than one week in vitr...
ORGANISM(S): Rattus norvegicus 
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