Background Wolf–Hirschhorn syndrome (WHS) is a contiguous gene deletion syndrome involving variable size deletions of the 4p16.3 region. Seizures are frequently, but not always, associated with WHS.

The goal of this analysis is to: Identify differentially expressed genes (DEGs) between PD patients and controls Perform gene set enrichment analysis (GSEA) Infer cell-type proportions using ...

Phase II study of neoadjuvant FLOT and chemoradiation for trimodality therapy of esophageal/GEJ adenocarcinoma. This is an ASCO Meeting Abstract from the 2025 ASCO Gastrointestinal Cancers Symposium.

Background: Microarray technology has brought significant advancements to high-throughput analysis, particularly in the comprehensive study of biomolecular interactions involving proteins, peptides, ...

Chromosomal microarray analysis (CMA) provides an opportunity to understand genetic causes of congenital heart disease (CHD). The methods for describing cardiac phenotypes in patients with CMA ...

Biomedical Engineering Department, McGill University, Montreal, Quebec H3A 2B4, Canada McGill Genome Centre, McGill University, Montreal, Quebec H3A 0G1, Canada ...

1 Cytogenetics Department, Quest Diagnostics Nichols Institute, San Juan Capistrano, CA, USA. 2 Medical Affairs Department, Quest Diagnostics, San Juan Capistrano, CA, USA. 3 Laboratory Medical ...

Denervation induces skeletal muscle atrophy, accompanied by complex biochemical and physiological changes, with potentially devastating outcomes even an increased mortality. Currently, however, there ...

Chromosomal microarray analysis enables the detection of microdeletions/duplications and has become the standard in clinical diagnostic testing for individuals with ...

Genetic abnormalities have been associated with 6 to 13% of stillbirths, but the true prevalence may be higher. Unlike karyotype analysis, microarray analysis does not require live cells, and it ...

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