United Kingdom: ME Research UK (MERUK) News

Discussion in 'General ME/CFS news' started by Andy, Feb 23, 2018.

  1. Andy

    Andy Retired committee member

    Messages:
    23,739
    Location:
    Hampshire, UK
    Funding announcement.

    Cause-effect relationships in the mitochondrial energy inefficiency in ME/CFS

    "We are very pleased to announce that ME Research UK has made a new award for PhD-level research. This project is being conducted at La Trobe University in Melbourne, Australia by PhD student Tina Katsaros under the supervision of Dr Sarah Annesley."

    https://www.meresearch.org.uk/research/cause-effect-relationships/
     
    Binkie4, Jacob Richter, obeat and 7 others like this.
  2. InitialConditions

    InitialConditions Senior Member (Voting Rights)

    Messages:
    1,852
    Location:
    North-West England
    ME Research Annual Report 2022 (published May 2023)
     

    Attached Files:

    MEMarge, RedFox, Hutan and 3 others like this.
  3. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    6,373
    Last edited: Jul 5, 2023
    Ash, Peter Trewhitt and Trish like this.
  4. Sly Saint

    Sly Saint Senior Member (Voting Rights)

    Messages:
    10,239
    Location:
    UK
  5. Andy

    Andy Retired committee member

    Messages:
    23,739
    Location:
    Hampshire, UK
    Binkie4, Ash, Amw66 and 8 others like this.
  6. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    6,373
    From Facebook:
    Our 2023 call for grant applications ended just over a week ago and we were delighted with the response – 24 high-quality applications from researchers around the world, and addressing a number of important research questions. Now begins the challenging task for our Science Committee to assess all these projects.

    Unfortunately they would only have the funds to fund a fraction of them.
     
    Binkie4, MEMarge, RedFox and 3 others like this.
  7. Andy

    Andy Retired committee member

    Messages:
    23,739
    Location:
    Hampshire, UK
    ME Research UK and Daphne Jackson Trust launch ME/CFS Fellowship

    "Applications are invited for a three-year Daphne Jackson Fellowship co-sponsored by ME Research UK. The Fellowship is open to talented researchers with a PhD – likely in a life science e.g. biomedical sciences, whole organismal biology, molecular genetics, infection and microbiology, structural biology, biological chemistry, who wish to return to research within a UK university or research institution after a career break of two or more years."

    https://www.meresearch.org.uk/me-research-uk-and-daphne-jackson-trust-launch-me-cfs-fellowship/
     
    Binkie4, MEMarge, RedFox and 6 others like this.
  8. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    6,373
    @meresearchuk ME Research UK has launched a new X/Twitter feed, namely, the ME Research UK - Reseacher Zone (@MEresearchzone) which will share information and resources for researchers in the field of ME/CFS. This will operate alongside the current general feed - @MEResearchUK but aimed at researchers, whether established or early career.

     
    MEMarge, RedFox, Ash and 1 other person like this.
  9. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    6,373
  10. Andy

    Andy Retired committee member

    Messages:
    23,739
    Location:
    Hampshire, UK
    RedFox, Binkie4, Starlight and 5 others like this.
  11. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    6,373
    Binkie4, Simon M, Amw66 and 2 others like this.
  12. Sly Saint

    Sly Saint Senior Member (Voting Rights)

    Messages:
    10,239
    Location:
    UK
    Merged thread - see also post #33 above.

    https://www.reed.co.uk/jobs/daphne-jackson-fellowship/51264608
     
    Last edited by a moderator: Sep 21, 2023
    Binkie4, MEMarge, Simon M and 2 others like this.
  13. Andy

    Andy Retired committee member

    Messages:
    23,739
    Location:
    Hampshire, UK
    Ongoing project: Exploring patterns of antibodies in moderate and severe ME/CFS

    "One possible route to the development of such a tool is to look at the pattern of antibodies produced by the body as part of the immune response, and the central idea behind Dr Lacerda and Prof. Cambridge’s study is that many of the features of ME/CFS could stem from the body’s immune system attacking its own damaged proteins following an infectious or toxic insult. These proteins may be damaged by an excess of toxic molecules (reactive oxygen species).

    An immune response is characterised by the production of antibodies, and Dr Lacerda and Prof. Cambridge plan to analyse the pattern of antibodies in samples from patients with moderate and severe ME/CFS (from the UK ME/CFS Biobank), linking them to changes in specific proteins. Their results may form the basis of new diagnostic tools for the disease, including stratification of patients based on severity."

    https://www.meresearch.org.uk/research/lacerda-061-info/
     
    Hutan, mango, DokaGirl and 7 others like this.
  14. MEMarge

    MEMarge Senior Member (Voting Rights)

    Messages:
    2,946
    Location:
    UK
    This sounds very interesting.
    It's presumably the Dr Cambridge that Jo Edwards has worked with from UCL.
     
  15. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    6,373
     
    Last edited: Oct 4, 2023
    EndME, Hutan, mango and 10 others like this.
  16. Ash

    Ash Senior Member (Voting Rights)

    Messages:
    1,884
    Location:
    UK
    I feel in my body like this is happening.
     
    MEMarge and Jacob Richter like this.
  17. duncan

    duncan Senior Member (Voting Rights)

    Messages:
    1,779
    If I had my druthers I'd throw one or two other chronic conditions into the mix of that study just posted by @Dolphin , e.g. MS and leprosy.

    ETA, Sorry, it was posted by @Andy
     
    Jacob Richter and Kitty like this.
  18. Jonathan Edwards

    Jonathan Edwards Senior Member (Voting Rights)

    Messages:
    17,060
    Location:
    London, UK
    Jo Cambridge has been working on this screening method for some time. It is a bit like a DecodeME for antibodies - looking across a very wide range then trying to make sure a signal is meaningful.

    Unfortunately Jo has been seriously unwell and is only just now getting through that.
     
    Lou B Lou, EndME, Hutan and 18 others like this.
  19. FMMM1

    FMMM1 Senior Member (Voting Rights)

    Messages:
    2,812
    Very interesting. The rituximab study [B-cell auto-antibodies] was relatively small & the [Fluge & Mella] Daratumumab [plasma cell auto-antibodies] study is very small (6 participants). Would a negative results for Daratumumab e.g. indicate that autoantibodies are not a common
    disease mechanism? Still, identifying a rare autoimmune case might give a clue to a more common [non-autoimmune] mechanism. So many questions ---

    Good to hear Jo's health has improved.
     
    Binkie4, Ash, MEMarge and 2 others like this.
  20. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    6,373
    ME Research UK

    ·
    ME Research UK is delighted to announce that we have awarded funding to Prof. Simon Carding at the Quadram Institute for a new project investigating the role of gut viruses in ME/CFS.

    The researchers plan a comprehensive analysis of the gut virome in people with ME/CFS, to identify signature viruses that might be involved in the development of the disease, and could represent a new biomarker. They will also look at whether they respond to microbiota transplantation therapy.

    Read more: https://www.meresearch.org.uk/research/carding-060
    More detailed description:
    https://www.meresearch.org.uk/research/carding-060-info

     
    Hutan, Chezboo, mango and 4 others like this.

Share This Page