So, it makes you think that, well, maybe that could have been one contributing factor to why we actually use genetic materials that incorporate ribose
because early cells that relied on an external source of ribose would have had easier access to that material compared to competing the cells that were looking for the different sugar that had a harder time getting across the membrane.
So it makes you think that, well, maybe that could have been one contributing factor to why we actually use genetic materials that incorporate ribose,
because early cells that relied on an external source of ribose would have had easier access to that material compared to competing the cells that we're looking for, a different sugar that had a harder time getting across the membrane.
Not exact matches
Because of the industry's
early ways of marketing, people thought
cell phones were free, when in essence the manufacturers hid behind the carriers, making wireless providers charge more in monthly fees so that their $ 700 phones would seem cheap.
Colin... Your entire diatribe proves my satirical and sarcastic point that I made
earlier... «
because a dog's coat gets thicker in the winter, therefore we came from a one -
celled amoeba».
I could go on and elaborate on a number of other disciplines or facts that creationists have to pretend into oblivion to retain their faith, including the Ice Ages, cavemen and
early hominids, much of microbiology, paleontology and archeology, continental drift and plate tectonics, even large parts of medical research (medical research on monkeys and mice only works
because they share a common ancestor with us and therefore our fundamental
cell biology and basic body architecture is identical to theirs).
(Babies born too
early often have a hard time breathing
because these
cells either haven't fully developed or can't produce enough surfactant.)
Now a University of Colorado Cancer Center study published online ahead of print in the journal Oncogene offers compelling evidence explaining this failure and offering a possible strategy for the use of retinoic acid or other retinoids against some breast cancers:
Because early clinical trials are often offered to patients who have already tried other more established therapies, breast cancer
cells may have been pushed past an important tipping point that offers retinoic acid resistance.
The key to Gather and Yun's biolaser is green fluorescent protein (GFP), a molecule that has proved endlessly useful to biologists since its discovery in the jellyfish Aequorea victoria in the
early 1960s, partly
because living
cells can be so easily programmed to produce it.
Because mice lacking both genes would not be born alive, the scientists followed up this lead by making «conditional knockout mice,» in which Esrp1 and Esrp2 activity was normal
early in fetal development, but then was switched off in skin epithelial
cells.
Lead author Moustafa Abdalla writes: «Almost all genomic studies of breast cancer have focused on well - established tumours
because it is technically challenging to study the
earliest mutational events occurring in human breast epithelial
cells.»
Because these organisms are excellent models for understanding stem
cell biology, researchers were able to shed light on the
earliest stages of follicle
cell differentiation, a previously poorly understood area of developmental biology.
«
Because of the Harvard Stem
Cell Institute, we were able to work with other researchers to make patient
cells into any type of neuron,» said Young - Pearse, whose lab spent two years fine - tuning protocols with collaborators to generate the neurons needed for her
early onset Alzheimer's study.
But many stem
cell scientists in Italy and abroad say it's too
early for such a study
because there is little to suggest that the therapy, whose details remain unpublished, might work.
Dr. Lyons and his team used zebrafish to study the formation of myelin sheaths by oligodendrocytes
because this laboratory animal is transparent at
early stages of its development, which allows investigators to directly observe
cells within the organism.
The finding, published
early online in the Journal of Biological Chemistry, is significant
because it helps explain how CBD works within the
cells.
Being fat makes all these diseases strike
earlier, and that seems to be at least in part
because fat
cells spur more inflammation.
But those
early attempts routinely failed
because, unless the donor was an identical twin, the host's immune system attacked the foreign stem
cells before they became established.
The researchers concluded that in the
early stages after stroke, improvements in voluntary movement can be attributed to a reduction in brain swelling
because of the trauma and other spontaneous repairs, while later improvements result from «neuronal plasticity» — the reorganization or regeneration of nerve
cells within the spinal cord in response to changes in the nerve network.
Stem
cells have been controversial
because scientists derive them from
early embryos or from fetal tissue.
Because tumor growth is a concern when
cells are reprogrammed to an
earlier stage of development, the researchers followed the mice in the Nature
Cell Biology study for nearly a year to look for signs of tumor formation and reported finding none.
«These results suggest that inflammation in mid-life may be an
early contributor to the brain changes that are associated with Alzheimer's disease and other forms of dementia,» said study author Keenan Walker, PhD, of Johns Hopkins University School of Medicine in Baltimore, Md. «
Because the processes that lead to brain
cell loss begin decades before people start showing any symptoms, it is vital that we figure out how these processes that happen in middle age affect people many years later.»
Because these
cells are taken from such an
early stage in development, they have the ability to become
cells of any tissue type (except for the whole embryo itself), making them pluripotent.
«These
cells would offer the hope of having a broader and more consistent ability to differentiate into a range of
cell types
because they are at an
earlier stage of development.
Earlier versions of such vaccines largely failed
because they targeted single invading substances that were not mutated, so T
cells that attack invaders often ignored them, he says.
But while substantial data (including AFFiRiS» [15] and Prothena's [20,22] preclinical work) give good reason to think that
early clearance of AS neuropathology will decelerate the rate of SN DA neuronal loss, astrocytosis, and possibly accumulation of senescent glial
cells in PD, there is no reason to think that doing so will prevent these phenomena entirely, if for no other reason than
because many other factors also contribute to their occurrence.
So when AFFiRiS» Schneeberger opines that «given the mode of action of disease modifiers», an AS - clearing immunotherapy such as PD01A (or PRX002) is «really something we need to apply
early in this disease»
because «once the the brain
cells are destroyed, getting them back is probably impossible,» he is adopting a view that is entirely reasonable — but only
because it is constrained to the specific plank in the integrated platform that rejuvenation biotechnology must become.
The L - arginine - induced pancreatitis is widely used as a relevant model for pre-clinical trials
because 1) it is reproducible, 2) it shows dose and time dependent acinar
cell necrosis, 3) it can be used for investigation of
early as well as late phase of acute pancreatitis, and 4) it is suitable for investigation of extra-pancreatic organ damage (pulmonary, hepatic renal and circulatory) and insulo - acinar axis [3].
The bottom line, says Daley, is that research on both types of stem
cells must continue,
because it's too
early to predict where the safest and most effective
cell - based therapies will come from.
These
early studies hold great promise
because without this transcription machinery, cancer
cells can not recover or function.
Under the proposed NIH policy, taxpayer funds would be allowed for experiments in which human
cells are added to
early - stage embryos of all animals except nonhuman primates, such as chimpanzees and monkeys,
because they are so similar to humans.
Among the
early germ
cell markers examined, VASA is a candidate gene for detecting pre-meiotic germ
cell differentiation from monkey ES
cells,
because its expression is detected
earlier in the primordial stage of germ
cell development in comparison to that of PIWI family genes in vivo in mice and humans [11], [36]--[38], [49].
Harold Varmus: Well the simplistic way to think about that is and I'm not sure this is the way it will be worked out, is to be able to take just a few
cells from those
early lesions and examine them genetically or for other kinds of marks on the DNA that would predict whether or not this is some - this is a lesion which might or an
early stage growth that might never be able to progress, but it is also possible that every
early tumor of that kind has some probability of expanding and invading and growing to become a medical problem, so getting that right will obviously be crucial
because it's very difficult to say when you've diagnosed something that is an
early stage tumor that it won't progress.
A new study suggests some preterm births occur
because the fetus rejects the mother, after its immune system is triggered too
early and senses maternal
cells as foreign invaders.
As the drug enters your system, it breaks down itself into small molecules that is enough to pass through your body's
cell mainly
because as mentioned
earlier, every
cell in our body have receptors for steroids called androgen receptor which is where the steroid molecules bind.
As the drug enters your system, it breaks down itself into small molecules that is enough to pass through your body's
cell mainly
because as mentioned
earlier, every
cell in our body have receptors for steroids called
They don't get cancer, but they're sicker overall
because they're less capable of detoxifying aflatxoin — leading to fun stuff like fatty liver, liver necrosis (
cell death), proliferation of bile duct tissue, and
early death.
You know,
early on I mean «Hey, I want them producing ketones and utilizing ketones
because of the incredible therapeutic facts it has on reducing cancer
cell division right.
HI lee RN after the ages of 24 to 27 the bodys enzyme production reduces to from a teaspoon to eyedopper levels we start to rely on the bodies own ability to assimilate and absorb its own enzyme source where as we can run through walls at 17 to 27 try to do ot at 37 0r 47 things do nt go as planned recovery takes longer a we age generally with poor diet and junk food shrinkage of organs increase as we age
because of the lack of enzymes that are active in the body fibrin scar tissue and debris as well as sludge in the blood require the following (number 1) is oxygen (number 2) is Enzymes (number 3) is electrolytes (Number 4) is negatively ionized (Red Blood
Cells) this is what is required to remove the excessive fibrin from the body Dr perlmutter is correct with his grain and carb theory however without systemic enzyme assistance and the other 3 protocols organ shrinkage and early aging are a reality the enzymes (systemic) do the major work eating up and ridding the excessive fibrin that is in the body and easy to see with microscopy as is Red Blood cells that are positively ionised (Stuck together) find it had to deliver ATP (cell food) that feed the cells One of the major causes of arterial blockages is inflamation condensed LDL triglycerides (bad cholestorol) not mistaking fluffy or non condensed LDL which is good for the brain and harmless as is HDL cholestorol l
Cells) this is what is required to remove the excessive fibrin from the body Dr perlmutter is correct with his grain and carb theory however without systemic enzyme assistance and the other 3 protocols organ shrinkage and
early aging are a reality the enzymes (systemic) do the major work eating up and ridding the excessive fibrin that is in the body and easy to see with microscopy as is Red Blood
cells that are positively ionised (Stuck together) find it had to deliver ATP (cell food) that feed the cells One of the major causes of arterial blockages is inflamation condensed LDL triglycerides (bad cholestorol) not mistaking fluffy or non condensed LDL which is good for the brain and harmless as is HDL cholestorol l
cells that are positively ionised (Stuck together) find it had to deliver ATP (
cell food) that feed the
cells One of the major causes of arterial blockages is inflamation condensed LDL triglycerides (bad cholestorol) not mistaking fluffy or non condensed LDL which is good for the brain and harmless as is HDL cholestorol l
cells One of the major causes of arterial blockages is inflamation condensed LDL triglycerides (bad cholestorol) not mistaking fluffy or non condensed LDL which is good for the brain and harmless as is HDL cholestorol levels
Motion Twin's upcoming Metroidvania roguelike Dead
Cells should be on your radar,
because it's really cool; I've enjoyed the Steam
Early Access version.
well i feel the same way but honey when u want something thts to expensive and u want it bad u ai nt got no choice but no to get it see i have a nintendo DSIxl and an ipod so if i keep up my ipod and game then thts shows me thats i might get it but if i do nt get he ipad which i know mygranny goin pay for it lik she did with ipod and game then i know shemight pay 500 lik she did for her
cell phone so if she say no then im goin be lik ok so u wont pay 500 for a big electronic but u can pay for a small thing u can get ayway but thts what i wouls say but i have no argue
because christmas is coming soon and u can wait by showing your mom tht your grades are good then just do nt think to hard or get the big ipad
because if u think hard then your mind is going to go to something else then your goona want bot so im jsut waiting till christmas or im may the sale cause it might drop to 300 in may the sale so i only got a couple months to wait inless i wait to the sale becaues my bp - day in july so te sale in may thats going to be an
early birthday gift so thanks for lettn me read this and sorry to take time but hey advise always help
Remember the
early days where Samsung produced
cell phones, and most of us dismissed them simply
because it failed to live up to expectations in terms of user interface and build quality?
Vaccinating
early is important
because pigs may be infected with mycoplasmal pneumonia during the first three weeks of life.3, 4 Research shows a positive correlation between prevalence at weaning and respiratory disease at finishing.5 In addition, research from the University of Minnesota shows that pigs have memory
cells from their dam that can respond successfully to mycoplasma vaccination when stimulated at a young age.6
Because the virus attacks the
cells that produce immunity (T and B - lymphocytes) dogs are always immuno - suppressed
early in the disease.
Since
cells can be exposed to growth factors
earlier in the healing process (in situations where they wouldn't otherwise be, either
because of necrosis or hypoxia or lack of bloodflow), the conversion of collagen types can be modulated and the subsequent formation of scars can be mitigated.
Early spaying may therefore, reduce occurrence of malignant lesions
because the procedure removes the source of the hormones that cause some mammary
cells to lose growth control, which puts these dividing
cells at high risk for mutation and malignant transformation by environmental carcinogens.In fact, recent reports have identified activation of a specific oncogene in a number of canine mammary tumors.
The demo featured at PAX was a very
early alpha, which was impressive
because it handled very well, and the minimalist
cell - shaded style looked phenomenal.
Motion Twin's upcoming Metroidvania roguelike Dead
Cells should be on your radar,
because it's really cool; I've enjoyed the Steam
Early Access version.