On April 15, 2013 the United States Supreme Court heard submissions on
whether human genes are patentable products of innovation or unpatentable products of nature.
Ultimately, the case will decide
whether human genes can indeed be patented in the United States.
Widely billed as a decision on
whether human genes can be patented in the US, the ruling actually applies to all DNA, from whatever species.
Widely billed as a decision on
whether human genes can be patented in the US, the ruling actually applies to DNA from any species.
Using abnormally - fertilised human embryos (I.e. With three sets of DNA instead of two), they have studied
whether the a human gene can be modified.
The degree of DNA similarity didn't necessarily indicate
whether a human gene could stand in for a yeast gene, Marcotte and colleagues reveal online today in Science.
Not exact matches
The principles that have emerged thus far are these: We should seek new knowledge of our
genes (and we can say this without deciding
whether the
Human Genome Initiative is the wisest and most cost - effective way to do so) We should seek therapies for the genetic disorders that afflict many people.
Before this can happen though, Teixeira said that his team will first have to determine
whether the Stk11
gene or the other
genes and proteins it controls are similarly affected in the
human form of BPH.
«The million dollar question is
whether mutations of this
gene also occur in
humans with cerebellar ataxia,» says Becker, who is screening people with genetic forms of the condition to find out.
Upon joining the lab, Lee chose a high - risk project — «it sounded like more fun,» she says — aimed at determining
whether a key
gene in the yeast cell cycle, cdc2, was also present in
human cells.
Further research would look at
whether mutations of the same
gene in
humans could contribute to depression.
Ressler then wanted to see
whether Oprl1 could be linked to PTSD in
humans, so looked at the
gene's sequence in approximately 1,800 highly traumatized civilians, some of whom had PTSD and others who did not.
GenInfo is well organized and easy to «browse,»
whether you need the new statement on cloning from the
Human Genome Organization or the new Swedish law concerning the use of gene technology on human be
Human Genome Organization or the new Swedish law concerning the use of
gene technology on
human be
human beings.
Whether their work is in
human genes, dwarf planets, or computer chips, many scientists have this in common: What they study is tangibly out there, somewhere.
To figure out
whether modern
humans use their
genes differently
«Gaining a better understanding of the functions
genes perform in cells,
whether plant or animal, is going to help us understand how to diagnose and treat diseases in
humans,» says Richard K. Wilson of Washington University.
The results show that the epigenetic pattern in more than 3,000
genes (out of approximately 25,000 that exists in a
human being) had changed differentially, depending on
whether the participants had eaten saturated fat or polyunsaturated fat.
But in September last year the team announced it had applied to conduct genome editing on these embryos — five months after researchers in China had reported experiments applying CRISPR — Cas9 genome editing to non-viable
human embryos, which sparked a debate about how or
whether to draw the line on
gene - editing in
human embryos.
The research showed the beta - lactamase
genes in Klebsiella pneumoniae were on all the time,
whether or not the bacteria were infecting
human cell cultures.
Rather than trying to understand
whether the
human condition can be broken down into
genes and quarks, he said, a big picture approach would contribute to more constructive engagements with evangelicals.
HIF regulates
genes that dictate how the
human body responds to a lack of oxygen, he said, but it can also affect
genes that determine
whether a cell divides and how that cell can affect neighboring cells.
One worry, for example, is
whether present - day computer programs will be powerful enough to distinguish
genes from the non-coding DNA that makes up 98 per cent of the
human genome.
Aside from dietary issues, the CMAH
gene also proves to be a major factor in
whether or not a transplanted organ from an animal would be accepted by a
human because of the
gene.
The
human genome contains about 3 billion base pairs, but only about 2 percent of these base pairs represent protein - coding
genes, meaning that whole - exome sequencing measures the genetic alterations focused on a small but very important fraction of the genome (as opposed to techniques of whole genome sequencing, which measures every nucleotide across the entire genome, regardless of
whether these
genes are expressed or silent).
The paper has split scientists, with consensus on the need for a moratorium on clinical applications but disagreement about
whether to support basic research on editing
genes in
human sperm, eggs, or embryos.
Regulatory debate Huang's team's April report spawned a flurry of scientific and policy meetings and statements as governments and policy experts wrestled with how or
whether to draw the line on
gene editing in
human embryos.
There is a long way to go before we can tinker with our
genes but tests have been done in
human embryos to find out
whether it can be safe and effective
To find out
whether Rh proteins perform a similar function, the team knocked out ammonium transporter
genes in yeast and replaced them with
human Rh protein
genes.
He and others have recently used
gene - editing tools to correct mutations in
human iPS cells but haven't used the same combination of methods or done the same set of experiments to determine
whether the iPS - derived cells are safe.
To determine
whether the reactivation of methylation - silenced
genes by EGCG is a general phenomenon that also occurs in other cell lines, we studied the effects of EGCG treatment on the methylation status and mRNA levels of p16INK4a or RARβ in three other
human cancer cell lines (Fig. 3C) ⇓.
They therefore went on to determine
whether there was also a link between the identified
genes and
human glioma.
Although CRISPR is incredibly useful for generating mutations by NHEJ and generating small mutations with HDR, when it comes to larger scale genome editing, such as replacement of a mouse
gene with its
human ortholog (greater than 5 kb), it remains to be seen
whether CRISPR is as robust as conventional
gene targeting.
In the current work we used adenoviral - type 5 (dE1 / E3)(Cytomegalovirus promoter) with
human ABCA10 transgene (Ad - h - ABCA10) purchased from Vector Labs ® in order to investigate
whether gene therapy can be used as a pre-treatment to enhance the efficiency of inhaled cisplatin.
To determine
whether or not increased DNA gain or loss likely had an evolutionary impact we compared
human and mouse
gene expression divergence.
These
genes likely came from the gametes — the eggs or sperm — and can be used to predict
whether an embryo is chromosomally normal or abnormal at the earliest stage of
human development.
There has been a rapidly increasing interest in
whether environmental factors modulate the establishment and maintenance of epigenetic modifications, and thereby affect
gene expression and phenotype in
humans and wildlife.
Their preservation in the zebrafish allows us to visualize in this transparent genetic vertebrate model
whether these variants are just neutral or if they disrupt the regulation of one the neighbor
genes, possibly revealing the actual
gene affected in AMD
human patients.
Whether humans will continue to evolve and rid themselves of the thrifty
gene remains to be seen.
Confirming this prediction for several dozen HARs, our next goal was to see
whether any of these HARs enhanced patterns of
gene activation that were uniquely
human.»
Having established the importance of the miR - 181a target
genes, Smad1 and Smad5, in BMP / GDF ligand - induced neurite growth, we next determined
whether miR - 181a - modulated Smad phosphorylation / activation and neurite growth in SH - SY5Y cells, which are a widely used cell line model of
human mDA neurons which also express the miR - 181a targets, BMPR2 and Smad1 / 5 [18,38].
We are identifying
genes that alter atherosclerosis susceptibility in a mouse model and testing
whether they play a role in coronary artery disease in
humans.
For example, Akey said, one new question we might ask about interbreeding between modern
humans and Neanderthals is
whether there were any sexual biases in that
gene flow.
Although the newest edition of the authoritative textbook, Vitamin D, claims that in
humans calcidiol binds with equal affinity to the DBP
whether it is derived from vitamin D2 or vitamin D3, 37 the citation for this statement is the author's own PhD thesis, in which he reported results obtained from testing the DBP of a mere two people.48 Since the
gene for the DBP is one of the most polymorphic known (meaning it exists in many forms), existing in three common alleles and 124 known rarer alleles (alleles are specific forms of the same
gene), each allele itself having many polymorphisms, 37 a sample size of two is rather unconvincing.