Quantitative Analysis of DNA Double‐Strand Breaks in Genomic DNA Using Standard Curve Method
This study presents a simple and cost‐effective method for quantifying DNA double‐strand breaks (DSBs) using standard curves based on Ct values from LM‐qPCR and the theoretical number of DSBs from enzyme‐digested DNA standards. Its simplicity, affordability, and high‐throughput capability make it a valuable tool for genotoxicity testing, environmental ...
Lihuang Guo +5 more
wiley +1 more source
A Long-Term Survival Case of Acute Myeloid Leukemia With MYC-Positive Double Minute Chromosomes. [PDF]
Yoshimaru R +10 more
europepmc +1 more source
Codon usage pattern of vertebrates genes and chromosome banding pattern.
Toshimichi Ikemura, Shin‐ichi Aota
openalex +2 more sources
ATAC‐seq in Emerging Model Organisms: Challenges and Strategies
Principle of ATAC‐seq (left), overview of arthropod species with published ATAC‐seq data (middle), summary of experimental design (right). ABSTRACT The Assay for Transposase‐Accessible Chromatin with sequencing (ATAC‐seq) is a versatile and widely utilized method for identifying potential regulatory regions, such as promoters and enhancers, within a ...
Duğçar Ebrar Erdoğan +13 more
wiley +1 more source
Familial translocation between chromosomes 3 and 10: meiotic segregation, diagnostics and clinical features of chromosomal imbalance. [PDF]
Vozilova AV +7 more
europepmc +1 more source
Calpain Proteases and the Evolving Signaling Network in Insect Embryonic Patterning
Insect embryonic Dorsal‐Ventral (DV) patterning relies on the BMP and Toll pathways to different extents. Calcium‐dependent cystein proteases of the Calpain family also exert an important function to pattern the DV axis. In Drosophila, Calpain A cleaves the Cactus/IkappaB inhibitor and modifies Toll signals in ventral regions of the embryo. In Rhodnius
Alison Julio, Helena Araujo
wiley +1 more source
Porto‐sinusoidal vascular disorder in a pediatric patient with prolidase deficiency: A case report
Abstract Prolidase deficiency (PD) is a rare autosomal recessive disorder affecting collagen turnover, leading to diverse clinical manifestations including dermatologic lesions, hepatosplenomegaly, and vascular anomalies. Liver involvement in PD is poorly understood, with few reported cases.
Melissa Castro +5 more
wiley +1 more source
Integrated cytogenetic and genomic profiling of the MDS-L cell line. [PDF]
Mestre J +9 more
europepmc +1 more source
Novel mutation associated with non‐compaction ventricular myocardium: A case report
ESC Heart Failure, EarlyView.
Yan Li +4 more
wiley +1 more source

