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A canine chromosome 7 locus that confers a high risk of compulsive disorder susceptibility has been identified.
A collaboration between the University of Massachusetts Medical School, the Cummings School of Veterinary Medicine at Tufts University and the Broad Institute at the Massachusetts Institute of Technology has identified a genetic locus on canine chromosome 7 which coincides with an inc…
New research published in Nature Genetics has identified two genes located on chromosome 7 and 17 respectively that have variants that increase the risk of fronto-temporal dementia (FTD). The study brought together a large international group of genetic scientists in order to collect …
A canine chromosome 7 locus that confers a high risk of compulsive disorder susceptibility has been identified through a collaboration between the Behaviour Service at the Cummings School of Veterinary Medicine, the Program in Medical Genetics at the University of Massachusetts Medica…
Yale researchers have been awarded a $320,000 grant from The Kiev Foundation to study new ways to treat Williams Syndrome, a rare, thus far incurable chromosomal disorder that causes cardiovascular and connective tissue problems. Williams Syndrome (WS) occurs in about 1 in 10,000 birt…
A collaboration between the University of Massachusetts Medical School, the Cummings School of Veterinary Medicine at Tufts University and the Broad Institute at the Massachusetts Institute of Technology has identified a genetic locus on canine chromosome 7 which coincides with an inc…
The SPOT-Light HER2 CISH " kit is a laboratory test that uses DNA probes to measure the number of copies of Her-2 gene on chromosome 17 in breast cancer cells by a chromogenic method. (Approved: 7/1/2008)
In a related article appearing in the July 15 issue of JAMA, researchers have identified the mechanism linked to the alteration of certain genes cited by Bredel et al in the previous study. Glioblastomas-uniformly fatal brain tumors-often have both monosomy (absence of 1 chromosome) o…
By applying a method that combines end-sequence profiling and massively parallel sequencing, we obtained a sequence-level map of chromosomal aberrations in the genome of the MCF-7 breast cancer cell line. A total of 157 distinct somatic breakpoints of two distinct types, dispersed and…
Subtelomeres are concentrations of interchromosomal segmental duplications capped by telomeric repeats at the ends of chromosomes. The nature of the segments shared by different sets of human subtelomeres reflects their high rate of recent interchromosomal exchange. Here, we character…