Not exact matches
McCallion's strategy to make sense of all this data looks at the active
genes in cells
affected by a disease, groups of
genes that interact with one another, their vulnerability to mutation and information from past scientific studies to filter more than a thousand
gene candidates for disease risk down to just a handful within any one implicated
region.
We have identified hundreds of genetic variations associated with autoimmune diseases that appear to
affect the activity of
genes in specific
regions of the genome, pointing to biological pathways that may be involved
in disease and which, ultimately, may be treatable with medication.»
Comparisons of the Neandertal genome to the genomes of five present - day humans from different parts of the world identify a number of genomic
regions that may have been
affected by positive selection
in ancestral modern humans, including
genes involved
in metabolism and
in cognitive and skeletal development.
Functional analyses indicate that MFSD12 encodes a lysosomal protein that
affects melanogenesis
in zebrafish and mice, and that mutations
in melanocyte - specific regulatory
regions near DDB1 / TMEM138 correlate with expression of ultraviolet response
genes under selection
in Eurasians.
We examined the biological pathways, or common links between
genes, that might be
affected in these 131
regions that were identified.»
In two of these
regions, the differences were attributable to alternative alleles of just one
gene: teosinte glume architecture (tga1) and teosinte branched (tb1), which
affect kernel structure and plant architecture.
The researchers found that MYC may
affect circadian rhythm and metabolism by promiscuously binding to promoter
regions in key
genes for maintaining these daily cycles.
Most of the mutations identified
in the new work land
in genes, but some
affect noncoding
regions of the genome.
During development, chromosomes are subject to chemical changes that don't
affect the nucleotide sequence but can turn
genes on or off; the best known example is methylation,
in which a methyl group is attached to specific DNA
regions.
And
in January 2009 another Nature Genetics paper found an association between high body mass index and a 45,000 base - pair deletion
in a
gene called NEGR1, which
affects neuronal growth
in the hypothalamus, a brain
region that regulates hunger and metabolism.
They hit pay dirt on chromosome 10, finding such a marker
in a
region with several
genes thought to
affect heart function.
Changes
in the regulatory
region of a single
gene may have had a profound
affect on human evolution.
A
region of the
gene that produces the PACAP38 protein has held nearly constant, even
in humans, presumably because the protein plays diverse roles
in neuron communication and is essential for normal development of the cerebellum,
affecting brain cell migration, for example.
For now, Stadler's team wants to focus on the
regions in which it found altered
gene numbers to see how the CNVs
affect gene and protein functions.
The study also demonstrates an association between NCAN variations with volumes of certain brain
regions in young adults and infants, suggesting that the
gene is able to
affect brain structure and function.
Although this compound exhibits a preference for AT - rich
regions, overall it is expected to
affect expression of a multitude of different
genes involved
in diverse biological functions.
The research team has identified four
genes that have not previously been associated to OCD: NRXN1, HTR2A, CTTNBP2 and REEP3 — all which are believed to
affect the synapses
in striatum, a
region of the barin where e.g. planning of movements is carried out.
These proteins
affect chromatin structure, often
in telomeric
regions, and thereby
affect transcription and silencing of various
genes...
Gene ontology analysis of the
genes affected across several tissues (Supplementary Fig. 8) shows enrichment for
genes in the extracellular
region and
genes involved
in nucleosome and chromatin assembly and
in protein — DNA complexes.
A new primer pair designed from the sequenced E
gene TV - 3 (f) and TV - 3 (r) was used to detect viral
genes in clinical samples collected from different
affected regions in China.
Although most adult leukemias involving MLL
affect a different part of the
gene, the breakpoints found
in infant leukemias and secondary leukemias occur predominantly
in the small
region altered by the bioflavonoids.
Unfortunately, LOH
regions tend to be kilobases or megabases
in size, containing dozens or hundreds of
genes, and identifying which ones are truly
affected in terms of cancer remains challenging.
Targeting different
regions of the
gene is also useful
in case the
gene has a weird mutation that you didn't know about (which could
affect the ability of the gRNA to bind).
But rather than changes
in doublesex itself, these studies revealed changes
in downstream targets of dsx, via changes to specific DNA sequences to which DSX protein binds
in the cis - regulatory
regions of the bric - a-brac and desatF
genes and
affecting sex differences
in abdominal pigmentation and pheromone production.
To truly understand and treat complex neuropsychiatric disorders, we need to know what behaviors are
affected, which brain
regions are involved, which
genes, molecules, and cell types
in these
regions might be involved, and how the environment
affects the propensity to develop these disorders.
June 4, 2015 New tool brings standards to epigenetic studies One of the most widely used tools
in epigenetics research — the study of how DNA packaging
affects gene expression — is chromatin immunoprecipitation (ChIP), a technique that allows researchers to examine interactions between specific proteins and genomic
regions.
By
affecting the rate of cell differentiation and
gene expression, thyroid hormones regulate the growth and migration of neurons, including synaptic development and myelin formation
in specific brain
regions.
However, researchers at the University of California — Berkeley wanted to find out if there might a genetic component that could predict how couple interactions
affect marital satisfaction.5 Specifically, the team decided to look at the 5 - HTTLPR polymorphism
in the promoter
region of the serotonin transporter
gene.
In relation to the association of infant attachment with a promoter polymorphism of the serotonin transporter gene, we have mentioned that gene expression may be affected by variation in the DNA sequence of the regulatory region of the gen
In relation to the association of infant attachment with a promoter polymorphism of the serotonin transporter
gene, we have mentioned that
gene expression may be
affected by variation
in the DNA sequence of the regulatory region of the gen
in the DNA sequence of the regulatory
region of the
gene.
Early life adversity and serotonin transporter
gene variation interact to
affect DNA methylation of the corticotropin - releasing factor
gene promoter
region in the adult rat brain