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ProteomicsThe Influences of ApoE Isoforms on Endothelial Adherens Junctions and Actin Cytoskeleton Responding to mCRP
Monomeric C-reactive protein (mCRP) plays a role in cerebrovascular damage mediated by apolipoprotein E4 (ApoE4) in Alzheimer's disease (AD) pathogenesis. Using proteomic profilings, we found altered cytoskeleton proteins in the microvasculature of AD brains, including increased levels of hyperphosp...
ORGANISM(S): Mus musculus (Mouse) Homo sapiens (Human) 
2025-05-06 | PXD051529 | Pride
Apolipoprotein e (apoe)  monomeric c-reactive protein (mcrp)  lim domain and actin binding 1 (lima1)  cd31 and pcd31  cerebrovascular  endothelia  f-actin  alzheimer’s disease (ad) 
MetabolomicsIn Vitro and In Vivo Metabolomic Profiling after Infection with Virulent Newcastle Disease Virus
Newcastle disease (ND) is an acute, febrile, and highly contagious disease caused by the virulent Newcastle disease virus (vNDV) worldwide. The disease causes serious economic losses to the poultry industry. However, the metabolic changes caused by vNDV infection remain unclear. The objective of thi...
2019-12-20 | MTBLS1115 | MetaboLights
Genomicsena-DATASET-MDACC-Yale-15-01-2015-22:06:45:013-91 - samples
To examined the reproducibility of nucleotide variant calls in replicate sequencing experiments of the same genomic DNA, we performed targeted sequencing of all known human protein kinase genes (kinome) (~3.3 Mb) using the SOLiD v4 platform. This data set contains 17 breast cancer samples that were ...
EGAD00001001209 | EGA
GenomicsReproducibility of variant calls in replicate next generation sequencing experiments
In this study, we examined the reproducibility of nucleotide variant calls in replicate sequencing experiments of the same genomic DNA. We performed targeted sequencing of all known human protein kinase genes (kinome) (~3.3 Mb) using the SOLiD v4 platform. Seventeen breast cancer samples were sequen...
EGAS00001000826 | EGA
GenomicsMDACC-Yale-breast-cancer
Data Access Committee EGAC00001000298
EGAC00001000298 | EGA
ProteomicsTranscriptomic and proteomic analysis of osteogenesis imperfecta disease-specific induced pluripotent stem cells
Background: Osteogenesis imperfecta (OI) is a rare genetic bone disease that causes bone fragility and growth deformities. OI-derived disease-specific induced pluripotent stem cells (iPSC) can reflect disease pathogenesis. Hence, investigating the pathogenesis of OI through OI-iPSCs holds significan...
ORGANISM(S): Homo Sapiens 
2025-06-19 | PXD065237 |
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