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hello my name is my initial kind of each candidate cornell university biomedical engineering i

work in laboratory a customisable king and that of our paper is which you're stress

i can't yourself stress that really a services be tried there are set

the motivation behind our work is to explore the treatment of circulating tumour cells to

prevent an instrument task

in basic terms may taxes occurs once cancer cells

detached from primary tumour

and enter the circulation

e circulating tumour cells or c t c and utilized circulation is high

and if you're within one that's able to travel into distinct issues and or secondary

two hours

for primary tumours

surgery radiation there is generally successful in the tumour

however once the test this occurs it is very challenging stops for cancer because very

small tumours termite pasties

more distinct issues under too small to detect and tree

it is this mess that's right that a standard so that

all that is currently exploring the idea of whether c d's can be treated in

the luxury to reduce the channel estimate

one there you take we are currently investigating straight

which is unique in that induces so that in a variety of cancer so i

s believes nearly all of a healthy cells on four

trail one that receptors expressed on cancer cell service

which can try arise in the presence of trail

signal for programs so that notice a utterances

one of the main differences between and result in the two remote requirement

and the vascular my requirement

if we which usually exposure

with sheer force is much greater in the literature in that interpretation

we were interested in addressing the question of whether exposure we would sure that how

cancer cells respond there you section three

the basis of our study was that we treated colin in prostate cancer cell trail

and then expose the cancer cell which you're stress

well we found was that we were fewer stress actually enhances the a i x

trail when compared to sell that are suppose that conditions

when we further increase the sheer force that cancer cell we're supposed to

word increase the amount of time that cancer cells work suppose we will show forces

percent variation in trails further

what about other draws it's we which you're stressed and the duration of or that

demonstrated by many kinds of problems

to test this we also treated cell that's rooms

and that using the treatment of cancer which induces cancer cells that using a different

mechanism for training

three along the surface was that there's the signal eight utterances where a person enters

the cell and interpolated the unit which can a basic seller prosody and do so

we discovered that we will shear stress had no measurable and that are sent induced

errors

whether solidworks suppose that conditions or due to stress but percentage of cell undergoing a

services remain the same

this indicates that and intonation patterns is specific to train three

we also perform studies proving the molecular mechanism this sense the station

when we definitely have had where within cancer cells which signals for trail and use

eight utterances

the entire a aren't responses at all

indicating that the sense that the station it real task at hand so where assistance

in addition to originate from

we look for changes in the expression of receptors on serves of cancer cells

what they're exposed if you stress or not

the number that receptors on the self service remain unaltered

future efforts will focus on examining which your trust best on the time position data

centres as well as spatial distribution of that researchers on cancer cells

the main conclusion of our study is that which you're stress exposure consent i can

result to train three

this can make trail an ideal candidate for the treatment of cancers task sizing the

latch the future studies also reveal the possibility that receptors on c d c service

which here

we are currently investigating strategies to control how these receptors response which you're stress now

or trail there

this includes a video

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