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We performed zero-order chemical cross-linking mass spectrometry experiments on reconstituted discoidal HDL and human HDL to determine the APOA1 orientations in these particles.
ORGANISM(S): Homo sapiens (Human) 
2019-04-09 | PXD009927 | Pride
Single cell gene expression profile of bronchoalveolar lavage fluid (BALF) cells from Apoa1-/- and Apoa1+/+ mice challenged with LPS and house dust mite
Apoa1, a safe harbor locus for therapeutic genome editing in the liver
Bulk RNA-seq of microglia from Apoa1 KO mice injected with ApoA-I protein intravenously
N39 APOA1-tdTomato drug screen
Neutrophils play important roles in inflammatory airway diseases. Here, we assessed whether apolipoprotein A-I (apoA-I) modifies neutrophil heterogeneity as part of the mechanism by which it attenuates acute airway inflammation. Neutrophilic airway inflammation was induced by daily intranasal admini...
ORGANISM(S): Mus musculus 
2024-07-29 | GSE234287 | GEO
Collect tissues from control C57kBL/6 and the following genetically engineered mice-apoE knockout,apoA1 knockout, apoA1 transgene, apoB knockout, LDLR knockout.Both male and female mice fed chow or atherogenic diet will be used. Animals from each group were pooled into 2 pools, one containing 4 mice...
ORGANISM(S): Mus musculus 
Clinical application of somatic genome editing requires therapeutics that are generalizable to a broad range of patients. Targeted insertion of promoterless transgenes can ensure that edits are permanent, broadly applicable, while minimizing risks of off-target integration. In the liver, the Albumin...
ORGANISM(S): Mus musculus 
2021-06-01 | GSE152993 | GEO
The aim of the present study was to obtain and characterize an in vitro model for endogenous APOA1 and PON1 long-time up-regulation in hepatocytes that can be further used to decipher the mechanism of their protective action. Cultured human hepatocytes (HuH-7 cell line) were transfected with CRISPR/...
ORGANISM(S): Homo sapiens 
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