Not exact matches
The Stanford team found, however, that mitochondrial
DNA levels were significantly elevated in plasma samples from a small
number of HD
patients.
The MGH team has assembled a large
number of DNA samples from HD
patients who contributed them for research to the Massachusetts HD Center Without Walls and through collaboration with the Huntington Study Group.
After analyzing both scans together for
DNA variants associated with differences between when each
patient's movement - associated symptoms first appeared and when they would have been expected based on the
number of CAG repeats, MGH CHGR investigator and lead author Jong - Min Lee, PhD, identified two locations on chromosome 15 where variants were significantly associated with either early or late symptom onset.
When they sequenced the iPS cell lines, they found higher
numbers of mitochondrial
DNA mutations, particularly in cells from
patients older than 60.
We've analyzed a
number of patients»
DNA to look for the mutation in the gene we [found].
In this study, researchers assessed the outcomes
of 280 prostate cancer (Cap)
patients, and reviewed the
DNA «fingerprints»
of each
patient's tumor (using the
patient's initial diagnostic core biopsy) to determine if gene copy
number alterations (CNAs), or breaks in CFSs, were related to a less positive response to treatment.
First author Baoshan Xu, Ph.D., a former postdoctoral research associate in the Gerton Lab now starting his own lab at Sun Yat - sen University in China, worked with Hua Li, Ph.D., to use computational methods to count the
number of copies
of ribosomal
DNA in normal and cancer cells
of 162
patients from the eight projects.
«Most
patients who had low copy
numbers of mitochondrial
DNA have a poordisease prognosis,» Guha said.
Dr. Rudolph's group is developing mouse lines that carry mutations found in
patients with schizophrenia — specifically copy
number variations, in which segments
of DNA are either duplicated or deleted.
DNA copy -
number analysis
of cfDNA
of patient 2 identified single copy loss at the BRCA2 locus (Supplementary Fig.