Cystic fibrosis is a rare inherited disease caused by mutations
in a single gene called cystic fibrosis transmembrane conductance regulator (CFTR) and affects 1 in every 2500 newborns in the UK and over 90000 people worldwide.
Cystic fibrosis is a hereditary disease caused by mutations
in a single gene called CFTR.
Not exact matches
In yeast, for example, they've found that increasing the activity of a
single gene,
called Sir2, can significantly extend life span.
His suspicionswas confirmed: the children had an identical defect — a missing
single nucleic acid,
called guanine —
in the
gene coding for leptin.
Other researchers had linked the ank mutation to mouse chromosome 15;
in this week's Science, Kingsley's team reports that it's a
single typo
in a previously unknown
gene, which they
called ank, that led to a protein about 10 % shorter than the normal version.
RNA sequencing of both
single and clustered CTCs from breast cancer patients identified several
genes expressed at elevated levels
in CTC clusters, one of which — a protein
called plakoglobin — also was overexpressed
in the primary tumors of patients with reduced survival.
The researchers found that the blond hair commonly seen
in Northern Europeans is caused by a
single change
in the DNA that regulates the expression of a
gene that encodes a protein
called KITLG, also known as stem cell factor.
Now researchers have identified a
single gene,
called fruitless (fru), as responsible for the development of male sexual behavior
in the fly.
Labs have started tackling the problem with a tool
called single - cell transcriptome analysis, which gives readouts of all the
genes that are active
in individual cells.
Different versions of
genes can vary at
single points
in their sequence, and these variations are
called SNPs.
The widely accepted RNA - world theory posits that RNA — the molecule that today plays roles
in coding, regulating, and expressing
genes — elevated itself from the primordial soup of amino acids and cosmic chemicals, eventually to give rise first to short proteins
called peptides and then to
single - celled organisms.
Most of the afflicted family members, but none of those who sleep normally, carry a
single base - pair mutation
in a
gene called hPer2, the researchers report 12 January
in a paper published online
in Science.
Now two research teams have spotlighted the middle ground, using so -
called gene chips to evaluate millions of bases of DNA
in a
single experiment.
Your feelings about brussels sprouts could come down to a
single gene: Researchers at the University of Connecticut found that people missing the receptor for a bitter chemical
called PROP tend to like veggies rich
in the compound.
Although mutations come
in many varieties, one type,
called nonsense mutations, involve the seemingly innocuous change of a
single letter
in the coded message — a change that causes the
gene's message to prematurely read «stop.»
The researchers discovered a
single letter variant located
in TP53, a
gene known to play a central role
in tumor biology and for accumulating so
called somatic mutations, during the development of cancer
in patients.
Since then, so -
called Omics technologies have flourished, allowing researchers, for example, to observe and quantify thousands of
gene products
in a
single tissue sample.
In findings appearing online today in Cell Stem Cell, researchers in the laboratory of Gladstone Investigator Yadong Huang, MD, PhD, describe how they transferred a single gene called Sox2 into both mouse and human skin cell
In findings appearing online today
in Cell Stem Cell, researchers in the laboratory of Gladstone Investigator Yadong Huang, MD, PhD, describe how they transferred a single gene called Sox2 into both mouse and human skin cell
in Cell Stem Cell, researchers
in the laboratory of Gladstone Investigator Yadong Huang, MD, PhD, describe how they transferred a single gene called Sox2 into both mouse and human skin cell
in the laboratory of Gladstone Investigator Yadong Huang, MD, PhD, describe how they transferred a
single gene called Sox2 into both mouse and human skin cells.
Studying a specific type of genetic variation
in the DNA sequences of wolves and domestic dogs -
called Single Nucleotide Polymorphisms (SNPs)- the scientists identified the transfer of dog
gene variants into wolf genomes.
We are using a new technique,
called single cell RNA sequencing, to isolate thousands of
single neurons from human brain tissue, study all the
genes that are expressed
in each individual cell, and make cell - to - cell comparisons between normal, early stage and late stage AD.
Lloyd Trotman's recent research path begins at his discovery some years ago that the loss of a
single copy of a master tumor suppressing
gene called PTEN is sufficient to permit tumors to develop
in animal models of prostate cancer.
Malaria infections that were slow to clear were also strongly associated with a
single - point mutation
in a P. falciparum
gene called kelch 13, an important validation of the recently discovered genetic marker (k13)
in the DNA of the malaria parasite.
These
single nucleotide polymorphisms (SNPs), as they are
called, were located
in the HAS2
gene.