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quotmy mother also has big breasts maybe its hereditaryquot full version published

watch quotmy mother also has big breasts maybe its hereditaryquot full version published in 4k ultra hd
the giant from the bahamas - the actual biggest back in bodybuilding - joel stubbs motivation - youtube

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genetically speaking there is only one human race not five

most people believe that there are 5 human races -- european african asian native american and oceanic but genetically this is pure nonsense you can be genetically similar or different from someone no matter what they look likeltbrgtltbrgthttp:alderinwritescomgenetically-speaking-there-is-only-one-human-raceltbrgtltbrgtracial prejudice and discrimination are at an all-time high especially since the election of trump as president over 80000 bombing threats have been made against jewish mosques in the last couple of years mass shootings continue to take place every few months with the shooters usually citing racial biases white nationalism is at an all-time high with believers boldly protesting in cities like portland but what if i told you all of these racial biases we hold are only cultural constructs and have no basis in scienceltbrgtltbrgtthere is only one human race: theres so much ambiguity between the races and so much variation within the races that the only real truth to hang your hat on
mutants genetic gladiators buying a new legandary mutant with coins and leveling up

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im disabled and sexy born different

a passionate advocate for body positivity is on a mission to challenge stigmas surrounding disability and body image by posting risqu photos of herself online alex dacy 25 from chicago was born with spinal muscular atrophy sma a progressive genetic disease that causes muscle wasting and mobility problems under the name wheelchair rapunzel alex has become an online advocate for disabled-body positivity often instagramming risqu photos of herself in her underwear to break the stigmas she has also become an entrepreneur - creating merchandise that raises awareness for disabled bodies
husband amp wife with thousands of tumours: born different

despite being born with neurofibromatosis that has left 90 of her body covered in tumour bubbles a woman has found the love of her life who just so happens to have the same condition 58-year-old gail appelgren inherited a severe form of neurofibromatosis nf from her mother at birth causing tumours to form on nerve tissue they can develop anywhere in the nervous system including on your brain and spinal cord often making the condition life-threatening since she was first diagnosed at 12 years old gail who lives in edmonton canada has received more than 40 surgeries to try and correct the thousands of tumours on her body and counter the skin cancer that has formed as a result over the years gail has been accused of being contagious and has been banned from public swimming pools because of the way she looks however her luck began to change in august 2010 when she met her now husband tim golumbia a fellow sufferer of the condition tim 55 was born with a more mild form of nf
can we cure genetic diseases by rewriting dna david r liu

in a story of scientific discovery chemical biologist david r liu shares a breakthrough: his lab039s development of base editors that can rewrite dna this crucial step in genome editing takes the promise of crispr to the next level: if crispr proteins are molecular scissors programmed to cut specific dna sequences then base editors are pencils capable of directly rewriting one dna letter into another learn more about how these molecular machines work -- and their potential to treat or even cure genetic diseases
deep blue sea 2 video 2018 - full hd movie for free hdbestnet

storyline:a brilliant billionaire named carl durant is experimenting on bull sharks which soon rebel to cause havoc for a group of scientistsuser reviews: i just dont understand why this film exists the first one was for me the best kind of shlock fun characters random and shocking deaths absurd plotit was undoubtedly stupid but it
modelling helped me embrace my rare condition born different

a 22-year-old cites his rare condition which affects his teeth hair and sweat glands with helping him become a model brooks ginnan from new york was born with ectodermal dysplasia a rare genetic disorder brooks told btv: quoti believe the statistic is about 1 in 100000 babies are born with this it is a condition that affects my teeth hairs sweat glands and a number of other aspects of my life the 22-year-old has now modelled- both catwalk and editorial - for brands around the world
the age of genetic wonder juan enriquez

gene-editing tools like crispr enable us to program life at its most fundamental level but this raises some pressing questions: if we can generate new species from scratch what should we build should we redesign humanity as we know it juan enriquez forecasts the possible futures of genetic editing exploring the immense uncertainty and opportunity of this next frontier
im finally ready to show the world my tumours born different

inspired by her son a woman with three serious medical conditions has shared her incredible her story of overcoming depression and accepting her physical appearance vanessa cornelio 25 was born with neurofibromatosis nf a genetic condition which causes tumours to grow on her nervous system as well as scoliosis and kyphosis which cause sideways and outward curvature of her spine her son daniel jr was also born with nf and vanessa says she has finally decided to speak out in the hope it will one day inspire him vanessa of glendale arizona told barcroft media: its hard to have what i have on my body and be okay because women around the world work out they have perfect bodies they have everything
the teenager with butterfly skin born different

a teenager whose skin is so fragile it bleeds and blisters as she sleeps has helped her parents raise 5 million for charity sohana collins morning routine takes longer than most: on schooldays the 16-year-old wakes up between 6-7am while her mum sharmila carefully unwraps sohanas bandaged arms then uses surgical needles to prick her daughters painful blisters before cleansing and moisturising sohanas paper-thin skin sohana suffers from epidermolysis bullosa a rare genetic condition commonly referred to as the butterfly syndrome because skin is as delicate as a butterflys wings
decoding the dna opportunity with anne wojcicki 23andme

anne wojcicki co-founded 23andme to empower consumers with their genetic information now 12 years after its founding hear from ceo wojcicki on the tremendous opportunities that can be unlocked by genetic testing
decoding the dna opportunity with anne wojcicki 23andme

anne wojcicki co-founded 23andme to empower consumers with their genetic information now 12 years after its founding hear from ceo wojcicki on the tremendous opportunities that can be unlocked by genetic testing
the besties with albinism born different

two teenage girls have become best friends due to both having albinism lucy carpenter 14 and sammy mccombe 13 from melbourne australia have a rare form of albinismthe mothers of the teenagers immediately noticed something was different about their children as soon as they were born but only received a diagnoses a few weeks after the pair first met as just babies when their mothers went to a support event for families with children with albinism after briefly losing contact they rekindled their friendship and have been inseparable ever since