Purpose: To develop a high resolution microarray based method to detect single- and multiexons gene deletions and duplications. Methods: We have developed a high-resolution comparative genomic ...
LA JOLLA, CA—Genetic mutations kick start cancers. Some mutations shuffle the genetic code, others come from the deletion of key genes. At La Jolla Institute for Immunology (LJI), researchers have ...
In a recent study published in the journal PLoS ONE, researchers investigated the effect of genetic variability based on accessory gene deletions on severe acute respiratory syndrome coronavirus 2 ...
Metabolic dysfunction-associated steatohepatitis (MASH) is a polygenic disorder influenced by multiple genes, but their specific roles in the progression of disease remain unknown. To address this gap ...
Extensive single Watson-Crick base pair mutations can occur in addition to duplication or deletion of an entire group of genes on chromosomal region 17p11.2. Potocki-Lupski syndrome is a condition ...
Loss of a small portion of chromosome 16, known as 16p11.2, is significantly associated with autism report researchers from the University of Chicago Medical Center, the University of Illinois at ...
Researchers at Rutgers and Emory University have gained new insights into how schizophrenia (SCZ) develops, by studying 3q29 deletion syndrome, which represents the strongest-known genetic risk factor ...
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