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graft versus host disease organoids were co-cultured with mesenchymal stem cells
ORGANISM(S): Homo sapiens (Human) 
2024-05-22 | PXD034822 | Pride
identifying the proteomic signature of ALS and how this is changed after treatment with MSC-EVs
ORGANISM(S): Homo sapiens (Human) 
2026-09-14 | PXD034824 | Pride
Rett syndrome (RTT) is a progressive neurodevelopmental disease often caused by mutations in the X-linked gene encoding methyl-CpG binding protein 2 (MeCP2). The mechanisms by which impaired MeCP2 induces the pathological abnormalities in the brain is not understood. To understand the molecular mech...
ORGANISM(S): Homo sapiens (Human) 
2021-09-08 | PXD013327 | Pride
Spinal muscular atrophy (SMA) is characterized by low levels of survival motor neuron (SMN) protein and loss of motor neurons (MN); however, the underlying mechanism that links SMN deficiency to selective motor neuronal dysfunction is still largely unknown. We present here, for the first time, a com...
ORGANISM(S): Homo sapiens (Human) 
2022-02-15 | PXD015115 | Pride
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