Haydn Kissick, PhD

@HaydnKissick

Assistant Professor at Emory University. Interested in all things Immunology!

Vrijeme pridruživanja: studeni 2018.

Tweetovi

Blokirali ste korisnika/cu @HaydnKissick

Jeste li sigurni da želite vidjeti te tweetove? Time nećete deblokirati korisnika/cu @HaydnKissick

  1. 2. velj

    Excited to have a new outstanding cancer immunologist to work with !

    Poništi
  2. 18. sij

    Great writeup of our recent work by from . Always nice when other people do a better job explaining your work than you!

    Poništi
  3. proslijedio/la je Tweet
    14. sij

    Letter from & co on "Reinvigorating NIH Grant Peer Review" | Encourages immunologists & colleagues throughout biomedical research funded by the NIH to take the “Once-a-Year” pledge & provides suggestions to improve grant study sections

    , , i još njih 4
    Poništi
  4. 19. pro 2019.

    Notice the small piles of chillies on the side if everyones plate. Spiiiiicy!!!

    Poništi
  5. 14. pro 2019.

    When the pre-activated T-cells find it, they can receive all the signals they need to become killers. Could be a 2-step process to stop over production of killers when only a localized response is needed. Still a lot to understand about this obviously.

    Prikaži ovu nit
    Poništi
  6. 14. pro 2019.

    When T-cells encounter these conditions, they might only activate enough to start scanning for regions of increased inflammatory signals such as these outposts in the tumor. This outpost is then a way to concentrate the limiting amounts of danger signals and antigen.

    Prikaži ovu nit
    Poništi
  7. 14. pro 2019.

    then travel to this structure to encounter antigen again before taking the final step of its differentiation. Seems like a bad design. My wild guess is that there is a lack of ‘danger signals’ or low concentrations of tumor antigen in the peripheral sites.

    Prikaži ovu nit
    Poništi
  8. 14. pro 2019.

    There is a perfectly good lymph node with dendritic cells joined directly to the cancer by blood/lymphatic vessels. Why go to the trouble of building an outpost of these cells in the tumor. It seems to me a T-cell would need to see antigen in a lymph-node,

    Prikaži ovu nit
    Poništi
  9. 14. pro 2019.

    Lots of questions to follow up on. Mechanisms that cause the generation, how tumors might inhibit to escape T-cell destruction, if these structures correlate with response to checkpoint therapy etc. etc. What I think is most interesting is why the immune system does this.

    Prikaži ovu nit
    Poništi
  10. 11. pro 2019.

    Thanks to all our friends and collaborators over the years who helped us with this work. This work was only possible with our outstanding physician and immunologist collaborators!

    Poništi
  11. 15. sij 2019.

    Check out the first article from our lab in ! Describing how novel non-coding RNAs undergo changes during T cell differentiation. Thousands of previously unannotated genes, many shared in human and mouse. Great work Will Hudson &

    Poništi
  12. 2. pro 2018.

    Thanks for all the kind welcomes, very excited to join all you friendly tweeters!

    Poništi

Čini se da učitavanje traje već neko vrijeme.

Twitter je možda preopterećen ili ima kratkotrajnih poteškoća u radu. Pokušajte ponovno ili potražite dodatne informacije u odjeljku Status Twittera.

    Možda bi vam se svidjelo i ovo:

    ·