Dumbacrats blow 8 million on sex changes for Mice, thank GOD for DOGE!!!

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Because, you see, sometimes, mice are born in the wrong body and identify as the other gender, therefore, we must spend BILLIONS to figure out this mystery. Excellent use of tax dollars dontcha think?
This is NOT about transgender mice, you drooling idiot, it is about transgenic mice to be used in medical research.
 
This is NOT about transgender mice, you drooling idiot, it is about transgenic mice to be used in medical research.
I'm sorry I made fun of the study. It is super important to help mice with gender dysphoria. I hope next we can try the same study on rabbits and other gender confused animals. You libs spend money on the greatest things! Also, whats with all the name calling? That seems like the trait of an angry, bitter, fat, walmart scooter riding Karen with chin hairs(on all 3 chins!).
 
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I can see how a person could misunderstand the programs meaning . I guess jow biden would of knew what it was for right ? Probally not to be honest .
Trump could fart and lefties would make it into something other then a fart
 
You said nothing when they spent other money researching drugs and vaccines to save lives.
Why is this a problem?
It's not as if their research was baseless and both you and Trump are experts in identifying waste.
what vacine were they working on boris that required trans gender mice . Please explain in detail or stfu because you have no clue what your talking about
 
what vacine were they working on boris that required trans gender mice . Please explain in detail or stfu because you have no clue what your talking about

maybe you have no clue what you are talking about..maybe you should..what is the acronym..ah yes..STFU..

"...the rapid expansion of the COVID-19 pandemic has made the development of a SARS-CoV-2 vaccine a global health and economic priority. Taking advantage of versatility and rapid development, three SARS-CoV-2 mRNA vaccine candidates have entered clinical trials with a two-dose immunization regimen. However, the waning antibody response in convalescent patients after SARS-CoV-2 infection and the emergence of human re-infection have raised widespread concerns about a possible short duration of SARS-CoV-2 vaccine protection. Here, we developed a nucleoside-modified mRNA vaccine in lipid-encapsulated form that encoded the SARS-CoV-2 RBD, termed as mRNA-RBD. A single immunization of mRNA-RBD elicited both robust neutralizing antibody and cellular responses, and conferred a near-complete protection against wild SARS-CoV-2 infection in the lungs of hACE2 transgenic mice. Noticeably, the high levels of neutralizing antibodies in BALB/c mice induced by mRNA-RBD vaccination were maintained for at least 6.5 months and conferred a long-term notable protection for hACE2 transgenic mice against SARS-CoV-2 infection in a sera transfer study. These data demonstrated that a single dose of mRNA-RBD provided long-term protection against SARS-CoV-2 challenge.


comrade stalin
bsc
 
or try this

from a real scientific journal..not some fake MAGA cesspool of ignorance

"...The research community is in desperate need of animal models for testing therapeutics and vaccines against coronavirus disease 2019 (COVID-19), and for studies aimed at understanding the molecular mechanisms of severe acute respiratory syndrome (SARS) coronavirus (CoV) 2 (SARS-CoV-2) infection and pathogenesis. A wide spectrum of laboratory and domestic animal species have been challenged with SARS-CoV-2 in an effort to find suitable models, but only a few, such as hamsters, cats, ferrets and monkeys, are susceptible<a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" title="Shi, J. et al. Susceptibility of ferrets, cats, dogs, and other domesticated animals to SARS–coronavirus 2. Science 368, 1016–1020 (2020)." href="https://www.nature.com/articles/s41596-020-00403-2#ref-CR1">1</a>,<a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" title="Rockx, B. et al. Comparative pathogenesis of COVID-19, MERS, and SARS in a nonhuman primate model. Science 368, 1012–1015 (2020)." href="https://www.nature.com/articles/s41596-020-00403-2#ref-CR2">2</a>,<a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" title="Sia, S. F. et al. Pathogenesis and transmission of SARS-CoV-2 in golden hamsters. Nature 583, 834–838 (2020)." href="https://www.nature.com/articles/s41596-020-00403-2#ref-CR3">3</a>. Unfortunately, many of these species are neither accessible nor practical for the vast majority of researchers to make rapid progress.

Mice are the most commonly used laboratory animals in biomedical research, and they have helped scientists develop diagnostics, therapeutics and vaccines for many human diseases. As such, it would have been easy to use mice for COVID-19 research if they were susceptible to SARS-CoV-2 infection, like humans, but that is not the case. One way to render mice susceptible to SARS-CoV-2 is to genetically modify them.


comrade stalin
bsc
 
Werbung:
maybe you have no clue what you are talking about..maybe you should..what is the acronym..ah yes..STFU..

"...the rapid expansion of the COVID-19 pandemic has made the development of a SARS-CoV-2 vaccine a global health and economic priority. Taking advantage of versatility and rapid development, three SARS-CoV-2 mRNA vaccine candidates have entered clinical trials with a two-dose immunization regimen. However, the waning antibody response in convalescent patients after SARS-CoV-2 infection and the emergence of human re-infection have raised widespread concerns about a possible short duration of SARS-CoV-2 vaccine protection. Here, we developed a nucleoside-modified mRNA vaccine in lipid-encapsulated form that encoded the SARS-CoV-2 RBD, termed as mRNA-RBD. A single immunization of mRNA-RBD elicited both robust neutralizing antibody and cellular responses, and conferred a near-complete protection against wild SARS-CoV-2 infection in the lungs of hACE2 transgenic mice. Noticeably, the high levels of neutralizing antibodies in BALB/c mice induced by mRNA-RBD vaccination were maintained for at least 6.5 months and conferred a long-term notable protection for hACE2 transgenic mice against SARS-CoV-2 infection in a sera transfer study. These data demonstrated that a single dose of mRNA-RBD provided long-term protection against SARS-CoV-2 challenge.


comrade stalin
bsc
I know what I am talking about for sure, bo9ris claim was no one complained about other projects that do vaccinees. Well, wepl b oris what vac was this for your so wise and smart same to the Fake Corney Stalin . Aka the 934u8983247398479334
 
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