Since the completion of the canine genome in 2005, science has been able to pinpoint
individual genes responsible for particular traits.
Not exact matches
The ability to locate the
individual gene or
gene sequence
responsible for each disease could revolutionize biomedicine in the 21st century.
According to studies, approximately one out of every 40
individuals in the United States is a carrier of the
gene responsible for spinal muscular atrophy (SMA), a neurodegenerative disease that causes muscles to weaken over time.
According to recent studies, approximately one out of every 40
individuals in the United States is a carrier of the
gene responsible for spinal muscular atrophy (SMA), a neurodegenerative disease that causes muscles to weaken over time.
While several studies in the intervening years have investigated whether particular
genes were
responsible for modifying HD onset, this is the first to employ genome - wide association (GWA) analysis, which scans an
individual's whole genome to identify chromosomal regions containing variants that are associated with the disease traits that are being studied.
Lisa Harris, of Dalton High School in New York City, won this year's top Siemens prize for
individuals — a $ 100,000 college scholarship — for developing a new method to detect carriers of a
gene responsible for cystic fibrosis.
But for a
gene therapy to be effective, one must know the precise
gene responsible for a given
individual's disorder and develop a tailored treatment.
Using a genome - wide association study (GWAS) that includes 1600
individuals living in Tanzania, Botswana, or Ethiopia, the authors identified regions of the genome that contribute to skin color variation and carried out a series of analyses to pinpoint the
responsible genes.
As it is well known that hypertension is a complex, multifactorial, quantitative trait under a polygenic control, 30 % to 50 % of the variation in blood pressure between
individuals is attributed to genetic factors, and the
genes responsible for susceptibility and blood pressure variation are mostly unknown.
A large body of research has reported that Nanog is allelically regulated — that is, only one copy of the
gene is expressed at any given time — and fluctuations in its expression are
responsible for the differences seen in
individual embryonic stem (ES) cells» predilection to differentiate into more specialized cells.
Other medical sequencing projects will use DNA sequencing to: discover new
genes that are involved in common diseases; identify the
genes responsible for dozens of relatively rare, single -
gene (autosomal Mendelian) diseases; sequence all of the
genes on the X chromosome from affected
individuals to identify those involved in sex - linked diseases; and survey the range of variants in
genes known to contribute to certain common diseases.
Instead, a supergene 4.5 million DNA letters long and composed of 125
individual genes seems
responsible for the peculiar behaviour of ruffs, report teams led by Burke and Leif Andersson, an evolutionary geneticist at Uppsala University in Sweden, in Nature Genetics.
It is neither nature nor nurture alone that is
responsible for brain chemistry and development; rather it is the interaction between both
genes and environment that is
responsible for the brain development of an
individual Research suggests that if a person has the
genes for schizophrenia, but doesn't experience the environmental factors necessary to «trigger» or express these
genes then the likelihood is low that they will develop schizophrenia.
McMaster University Scientists have published 2 studies identifying which
gene is
responsible for causing brain development disorders when several
genes are deleted in an
individual's genome, providing a path forward for developing new therapies.
Personalized Genome Sequencing Reveals Coding Error Johns Hopkins Kimmel Cancer Center scientists used «personalized genome» sequencing on an
individual with a hereditary form of pancreatic cancer to locate a mutation in a
gene called PALB2 that is
responsible for initiating the disease.
The
genes responsible for many genetic diseases are «recessive,» which means that two copies of a damaged
gene, one from the mother and one from the father, must be present in an
individual for the disease to occur.
Behrens, who co-chairs his firm's public policy practice group, said defense attorneys are already becoming more aggressive and citing other factors that may be
responsible for an
individual suffering from mesothelioma, including the BAP1
gene.