Results 1 to 10 of about 87,804 (313)

Clinical application of liquid biopsy in cancer patients

open access: yesBMC Cancer, 2022
Background This study was to determine the prevalence and clinical significance of clonal hematopoiesis (CH)-related variants, and somatic and germline mutations in cancer patients and healthy individuals.
Chieh-Min Chang   +7 more
doaj   +1 more source

Therapeutic and immunomodulatory potential of pazopanib in malignant phyllodes tumor

open access: yesnpj Breast Cancer, 2022
Malignant phyllodes tumors (PT) are rare aggressive fibroepithelial neoplasms with high metastatic potential and lack effective therapy. We established a patient-derived xenograft (PDX) and cell line model (designated MPT-S1) of malignant PT which ...
Dave Yong Xiang Ng   +20 more
doaj   +1 more source

Cell-Free miR-27a, a Potential Diagnostic and Prognostic Biomarker for Gastric Cancer [PDF]

open access: yesGenomics & Informatics, 2015
MicroRNAs (miRNAs) have been demonstrated to play an important role in carcinogenesis. Previous studies revealed that miRNAs are present in human plasma in a remarkably stable form that is protected from endogenous RNase activity.
Jong-Lyul Park   +4 more
doaj   +1 more source

Concurrent mapping of multiple epigenetic marks and co-occupancy using ACT2-seq

open access: yesCell & Bioscience, 2021
Background Genome-wide profiling of epigenetic marks is a core technology in molecular genetics. Co-occupancy of different epigenetic marks or protein factors at the same genomic locations must often be inferred from multiple independently collected data
Benjamin Carter   +3 more
doaj   +1 more source

Mutation profile of non-small cell lung cancer revealed by next generation sequencing

open access: yesRespiratory Research, 2021
Background Precision therapy for lung cancer requires comprehensive genomic analyses. Specific effects of targeted therapies have been reported in Asia populations, including Taiwanese, but genomic studies have rarely been performed in these populations.
Ya-Sian Chang   +7 more
doaj   +1 more source

Infection of Brain Organoids and 2D Cortical Neurons with SARS-CoV-2 Pseudovirus

open access: yesViruses, 2020
Since the global outbreak of SARS-CoV-2 (COVID-19), infections of diverse human organs along with multiple symptoms continue to be reported. However, the susceptibility of the brain to SARS-CoV-2, and the mechanisms underlying neurological infection are ...
Sang Ah Yi   +8 more
doaj   +1 more source

Multiregion sequencing of sarcomatoid renal cell carcinoma arising from autosomal dominant polycystic kidney disease

open access: yesMolecular Genetics & Genomic Medicine, 2022
Background Autosomal dominant polycystic kidney disease (ADPKD) is an inherited cystic kidney disease associated with a spectrum of various renal and extrarenal manifestations, including increased risk of kidney cancers.
Elizabeth Lee   +12 more
doaj   +1 more source

Polygenic risk score trend and new variants on chromosome 1 are associated with male gout in genome-wide association study

open access: yesArthritis Research & Therapy, 2022
Background Gout is a highly hereditary disease, but not all those carrying well-known risk variants have developing gout attack even in hyperuricemia status.
Ya-Sian Chang   +8 more
doaj   +1 more source

scPCOR-seq enables co-profiling of chromatin occupancy and RNAs in single cells

open access: yesCommunications Biology, 2022
scPCOR-seq is a single-cell sequencing technique that enables simultaneous profiling of genome-wide chromatin protein binding or histone modification marks and RNA expression in the same cell.
Lixia Pan   +4 more
doaj   +1 more source

Hi-TrAC reveals division of labor of transcription factors in organizing chromatin loops

open access: yesNature Communications, 2022
It is currently not clear how architectural proteins orchestrate chromatin looping at different scales of genome organisation. Here the authors report Hi-TrAC as a proximity ligation-free method to profile genome-wide chromatin interactions at single ...
Shuai Liu   +4 more
doaj   +1 more source

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