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ME Research UK: Role of Sirt1/NOS axis in vascular and immune homeostasis: a missing piece in the ME/CFS puzzle?

Discussion in 'ME/CFS research' started by Andy, Aug 21, 2019.

  1. Andy

    Andy Committee Member

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    Location:
    Hampshire, UK
    http://www.meresearch.org.uk/our-research/sirt1-nos-axis/

    https://twitter.com/user/status/1163390146156400641
     
    Andy, Aug 21, 2019
    #1
    Marky, Barry, hinterland and 22 others like this.
  2. Saz94

    Saz94 Senior Member (Voting Rights)

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    How long will it take to get the results of this?
     
    Saz94, Aug 21, 2019
    #2
    Barry likes this.
  3. Hoopoe

    Hoopoe Senior Member (Voting Rights)

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    I often think that I have some sort of inflammation going on, in different body parts. It feels like mild inflammation at least. Maybe it's not the c-reactive protein kind of inflammation. Something is happening there but it's not clear what.

    Is there a list of processes that feel like inflammation but aren't considered inflammation in the strict sense?
     
    Hoopoe, Aug 21, 2019
    #3
    andypants, alktipping, Saz94 and 2 others like this.
  4. Trish

    Trish Moderator Staff Member

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    55,414
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    UK
    A wild guess, a couple of years minimum?

    Say, at best, a few months to do the experiments, then six month to a year to analyse the results and write the paper, given that academics have a lot of other responsibilities as well, then a few months to find a journal to accept the submission, a few more months for the paper to be peer reviewed and if necessary the paper amended, then a few more months for the journal to get around to publishing it.
     
    Trish, Aug 21, 2019
    #4
    Barry, MEMarge, alktipping and 3 others like this.
  5. InitialConditions

    InitialConditions Senior Member (Voting Rights)

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    Location:
    North-West England
    Most academic research projects have a timeline of roughly three years, with results expected in the third year. This is of course variable.
     
    InitialConditions, Aug 21, 2019
    #5
    alktipping, Trish, ME/CFS Skeptic and 2 others like this.

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