Normal mice produced more than four times more melanocytes than did the p53 «knockout» mice.
In that time,
the normal mice produced regularly, giving birth to a litter of seven or eight pups approximately every 21 days, for a total of about 60 baby mice.
Not exact matches
Cells engineered to
produce insulin under the command of a smartphone helped keep blood sugar levels within
normal limits in diabetic
mice, a new study reports.
Damaged
mouse sciatic nerves
produced hundreds of times the
normal amount of two «chemoattractant» molecules, Cxcl1 and Cxcl2, which attach to the surfaces of neutrophils and draw the immune cells into injured tissue.
Using the refrigerated sperm, the researchers were able to fertilize an egg in vitro and
produce a
normal mouse pup.
Uhl and crew then
produced mice that had half the
normal number of opiate receptors and as a result, experienced greater discomfort when exposed to a standard mildly painful stimulus.
When they examined
mice genetically incapable of
producing Helios, they found the animals beset by a T - cell and antibody attack on
normal tissue.
In those
mice, but not in
normal mice, they found that caerulein caused existing alpha cells in the pancreas to differentiate into insulin -
producing beta cells.
That's because the boosted
mice produced normal — rather than high — levels of the amyloid precursor proteins from which plaques are made.
Six pairs of
mice — with one
mouse engineered to
produce gobs of human A-beta and one
normal — were surgically joined for a year, causing blood mingling that's far more extensive than that of a blood transfusion.
In a study published October 30 in Neuron, the scientists show that
mice genetically altered so they don't
produce serotonin didn't scratch as much as
normal mice when exposed to irritants.
But the males — despite having smaller testes and lower sperm counts than
normal mice — were clearly fertile and
produced offspring.
However, when the researchers knocked out SIRT1 in endothelial cells of 10 - month - old
mice, then put them on a four - week treadmill running program, they found that the exercise did not
produce the same gains seen in
normal 10 - month - old
mice on the same training plan.
«Just one transplant of the human EPO -
producing cells treated kidney anaemia in
mice, keeping their haemoglobin levels in the
normal range for the remaining 7 - month lifespan of the animals,» says Kenji Osafune, of Kyoto University in Japan, who led the team.
The researchers studied both
normal mice and
mice genetically engineered without the Trpv4 gene (which
produces TRPV4 channel protein).
In contrast, M49, a less virulent strain of strep, caused larger skin lesions in
mice lacking cathelicidin than in
normal, cathelicidin -
producing mice.
UBC Psychiatry Professor Dr. Weihong Song and Neurology Professor Yan - Jiang Wang at Third Military Medical University in Chongqing attached
normal mice, which don't naturally develop Alzheimer's disease, to
mice modified to carry a mutant human gene that
produces high levels of a protein called amyloid - beta.
All of the
mice produced normal amounts of SOX2 during development, when the transcription factor plays a critical role in the genesis of embryonic and neural stem cells.
In
normal mice with working photoreceptors (PR driven), stimulating the retina
produces a variety of responses in retinal ganglion cells, the output of the eye.
Photoswitches inserted into retinal ganglion cells (RGC) of blind
mice produce much less variety of response (all evenly red means the cells fire at the same time), while blind
mice with photoswitches inserted into bipolar cells (ON - BC driven) exhibit much more variety in their retinal response to light, closer to that of
normal mice.
(
Normal and engineered
mice produced the same volume of urine.)
Since more Cx43 means less room in the bladder, the team speculates that although
normal mice didn't stop
producing urine when asleep, their bladders were able to hold more due to decreased Cx43 concentrations.
To overcome this hurdle, researchers genetically engineered human T cells to
produce a CAR protein that recognizes a glycopeptide found on various cancer cells but not
normal cells, and then demonstrated its effectiveness in
mice with leukemia and pancreatic cancer.
Mice genetically engineered not to produce a key cytokine (TNF - alpha) fared no better than normal mice during infecti
Mice genetically engineered not to
produce a key cytokine (TNF - alpha) fared no better than
normal mice during infecti
mice during infections.
KLF15 - deficient
mice produced 40 to 50 percent less bile acid than
normal mice, making them less capable of absorbing the lipids and the nutrients they contained.
The researchers found that levels of a substance called 4 - ethylphenylsulfate that is
produced by gut bacteria increased 46-fold in the
mice with autistic symptoms, but returned to
normal after treatment with B. fragilis.
In the
normal mice, UV treatment doubled the amount of KITLG
produced, whereas the p53 knockouts couldn't
produce any.
He notes, however, that other attempts to stimulate bone growth in
mice by manipulating cell signaling proteins have
produced denser than
normal bones — and he's surprised that Helms's team didn't see the same.
In another experiment,
mice lacking the cells that
produce serotonin scratched less than
normal mice when exposed to a skin irritant.
The acrosome, a structure essential for fertilization, appears as a green, moon - shaped cap on
normal sperm (left), but is missing or misshapen on sperm
produced by
mice treated with NB - DNJ (right).
The researchers found that in genetically - modified
mice lacking Interferon - 1, who were also fed a high - fat diet, the CD8 + T cells did not
produce an inflammatory response, and the
mice had near
normal blood sugar levels.
But Hecht notes that although CNP breaks down within minutes in the body, decoy FGFR3 lasts for hours and
produces normal growth in the
mice with just twice - weekly injections.
As seen through a microscope, the leg bone of a
normal mouse (left) makes considerably less new bone than a
mouse that
produces high levels of a signaling protein, WNT7B, that stimulates new bone growth (shown in pink on the right).
Dr. Verdin further found that prolonged intake of a high - fat diet, even in
normal mice, can itself reduce the activity of the enzyme
produced by SIRT3 — an enzyme his laboratory originally discovered.
Allergic airway hyperresponsiveness - enhancing γ $ ẹlta $ T cells develop in
normal untreated
mice and fail to
produce IL - 4 / 13, unlike Th2 and NKT cells.
When the sperm then fertilises a
normal egg, a transgenic
mouse is
produced with the same foreign DNA in every cell.
AHR - Enhancing γ $ ẹlta $ T Cells Develop in
Normal Untreated
Mice and Fail to
Produce IL - 4 / 13, Unlike TH2 Cells and NKT Cells.
When
normal mice were exposed to TNF, all tissues studied (liver, kidney, spleen, thymus, colon, and lymph nodes)
produced large amounts of A20 and the
mice survived unharmed.
Researchers comparing
normal and obese
mice found that obese
mice produced more than twice as much of a small microRNA molecule called microRNA - 143 in their liversANCHOR.
She observed that the repertoire of immune cell subtypes differed between
normal and engineered
mice, and furthermore, that T cells of engineered
mice fed a «western» (fatty) diet
produced inordinately high levels of pro-inflammatory cytokines.
Takeda et al. engineered
mice that were either unable to
produce a particular LPA receptor on their T - cells, or that
produced less LPA than
normal.
Conversely,
mice genetically engineered to
produce less insulin had healthier fat cells, burned off more calories, and resisted weight gain, even when given a diet that makes
normal mice fat.
The reason for this response, Gordon says, was twofold: Firmicutes bacteria transplanted from the fat
mice produced more of the enzymes that helped the animals extract more energy from their food, and the bacteria also manipulated the genes of the
normal mice in ways that triggered the storage of fat rather than its breakdown for energy.