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UnknownSodium para-aminosalicylic acid inhibits manganese-induced NLRP3 inflammasome-dependent pyroptosis by inhibiting NF-κB pathway activation and oxidative stress.
Not available
S-EPMC7670624 | biostudies-literature
UnknownColoration differences in three Camellia reticulata Lindl. cultivars: 'Tongzimian', 'Shizitou' and 'Damanao'.
Not available
S-EPMC10759361 | biostudies-literature
UnknownA recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China.
Not available
S-EPMC7079413 | biostudies-literature
ProteomicsProteomic analysis of differentially expressed proteins in the serum of patients with acute renal allograft rejection using iTRAQ labelling technology
Transplantation is currently the best treatment option for end-stage renal disease (ESRD) patients. However, acute rejection (AR) is the main source of failure in renal transplantation. The current gold standard for diagnosis of AR involves renal biopsy, but it is invasive, time consuming, costly an...
ORGANISM(S): Homo sapiens (Human) 
2021-09-08 | PXD015336 | Pride
Proteomics Acute rejection Serum Renal allograft Itraq 
ProteomicsGenotyping, generation and lysine 2-hydroxyisobutyrylation identification of the first human autosomal dominant osteopetrosis type II specific induced pluripotent stem cells
Background: Autosomal dominant osteopetrosis type II (ADO2) is a rare human genetic disease that has been broadly studied as an important osteopetrosis model; however, there are no disease-specific induced pluripotent stem cells (ADO2-iPSCs) that may be valuable for understanding the pathogenesis an...
ORGANISM(S): Homo sapiens (Human) 
2022-02-15 | PXD014227 | Pride
Osteopetrosis Whole exome sequencing Ipscs 2-hydroxyisobutyrylation Clcn7 
UnknownSHG/TPEF-based image technology improves liver fibrosis assessment of minimally sized needle biopsies.
Not available
S-EPMC6661026 | biostudies-literature
UnknownCorrelation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China.
Not available
S-EPMC8479922 | biostudies-literature
ProteomicsA qualitative proteome-wide lysine crotonylation profiling reveals protein modification alteration in the leukocyte extravasation pathway in systemic lupus erythematosus
Background Systemic lupus erythematosus (SLE) is a severe systemic autoimmune disease with multiple manifestations. Lysine crotonylation (Kcr) is a newly discovered post-translational modification (PTM) epigenetic pattern which may affect gene expression and linked to diseases causally. Methods We ...
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD042217 | Pride
Systemic lupus erythematosus  proteome  crotonylation  post-translational modifications  leukocyte extravasation 
Unknownvon Hippel-Lindau Protein Maintains Metabolic Balance to Regulate the Survival of Naive B Lymphocytes.
Not available
S-EPMC6660606 | biostudies-literature
UnknownIdentification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis.
Not available
S-EPMC9169345 | biostudies-literature
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