Colorectal cancer (CRC) remains one of the leading causes of cancer-related mortality globally. The standard methods for assessing MSI and dMMR are polymerase chain reaction (PCR) and 4-antibody immunohistochemistry (IHC).

The study isolated human pancreatic islet-derived mesenchymal stem cells (hPD-MSCs) from donor islets using lentiviral transduction of human telomerase reverse transcriptase. These cells were subsequently identified as adipogenic and osteogenic

To address food security challenges and climate change, the polyploid wild rice Oryza alta has been explored as a potential crop, although it suffers from seed shattering. We employed mesoporous

Magnetic nanoparticles (MNPs), due to their magnetic properties, can be activated by alternating magnetic field heating or unheated low frequency magnetic fields, thereby exerting intrinsic therapeutic effects or promoting drug

This study aims to perform a prenatal genetic diagnosis of a high-risk fetus with trisomy 7 identified by noninvasive prenatal testing (NIPT) and to evaluate the efficacy of different genetic

As the demand for WES increases and the cost of NGS decreases, WES, as a technique, requires a generous understanding of how experimental design can improve data interpretation and thus

IgG4-related disease (IgG4-RD) has complex clinical manifestations ranging from fibrosis and inflammation to deregulated metabolism. The molecular mechanisms underpinning these phenotypes are unclear. To investigate the transcriptomic changes in IgG4-RD

In this study, transcriptome sequencing of the whole fermentation course was perf ormed to explore the synthesis and regulation mechanism of AprE in B. licheniformis AQ. During the fermentation process,

The purpose of this study was to compare the chloroplast genomes of T. sinskajae and T. monococcum accession k-20970 and clarify the phylogenetic relationships between einkorn wheats via GeneMind GenoLab M

Targeted genomic sequencing (TS) greatly benefits precision oncology by rapidly detecting genetic variations with better accuracy and sensitivity owing to its high sequencing depth. Multiple sequencing platforms and variant calling