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UnknownE-cadherin Downregulation and microRNAs in Sporadic Intestinal-Type Gastric Cancer.
Not available
S-EPMC6769612 | biostudies-literature
UnknownDigital PCR identifies changes in CDH1 (E-cadherin) transcription pattern in intestinal-type gastric cancer.
Not available
S-EPMC5386649 | biostudies-literature
UnknownE(3)-equivariant graph neural networks for data-efficient and accurate interatomic potentials.
Not available
S-EPMC9068614 | biostudies-literature
UnknownInsights on conducting digital patient and public involvement in dementia research during the COVID-19 pandemic: supporting the development of an "E-nabling digital co-production" framework.
Not available
S-EPMC9321274 | biostudies-literature
UnknownStructure-based modeling reveals molecular basis for CYP153A6's novel activity toward toluene derivatives.
Not available
S-EPMC12932734 | biostudies-literature
UnknownWhole cells of recombinant CYP153A6-E. coli as biocatalyst for regioselective hydroxylation of monoterpenes.
Not available
S-EPMC9046528 | biostudies-literature
TranscriptomicsGenome profile of human rectal tumors and response to neoadjuvant chemoradiotherapy
Background: Neoadjuvant chemoradiotherapy (NCRT) is the treatment of choice in advanced rectal cancer, even though there are many patients who will not benefit from it. There are still no effective methods for predicting which patients will respond or not. The present study aimed to define the genom...
ORGANISM(S): Homo sapiens 
2011-11-17 | E-GEOD-25885 | biostudies-arrayexpress
ProteomicsEndogenous interactors of the natural trapping mutant TMX5/TXNDC15
The endoplasmic reticulum (ER) is the organelle of nucleated cells that produces lipids, sugars and proteins. More than 20 ER-resident members of the Protein Disulfide Isomerase (PDI) family regulate formation, isomerization and disassembly of covalent bonds in newly synthesized polypeptides. The PD...
ORGANISM(S): Homo sapiens (Human) 
2024-09-27 | PXD054716 | Pride
Endoplasmic reticulum  erp44  mixed disulfides  pdi family  tmx5/txnd15 
ProteomicsClients of membrane-bound PDI family members
The client-specificity of TMX3, TMX4 and TMX5 in cellula, was assessed by expressing mutant forms of the enzymes, where the last cysteine residue of the TMX’s CXXC catalytic sites has been mutated to alanine, which stabilizes the mixed disulfide that oxidoreductases establish with clients. Clients r...
ORGANISM(S): Homo sapiens (Human) 
2023-06-12 | PXD041156 | Pride
Trapping mutants Endoplasmic reticulum Oxidoreductases Mixed disulfides 
UnknownAnomalous non-equilibrium response in black phosphorus to sub-gap mid-infrared excitation.
Not available
S-EPMC9106664 | biostudies-literature
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