Mitochondrial Research

Monday: 09:00 - 17:00
Tuesday: 09:00 - 17:00
Wednesday: 09:00 - 17:00
Thursday: 09:00 - 17:00
Friday: 09:00 - 17:00
Saturday: -
Sunday: -

About Mitochondrial Research

All of the latest news and updates from the Wellcome Trust centre for Mitochondrial Research at Newcastle University.

Mitochondrial Research Description

The Wellcome Trust Centre for Mitochondrial Research is built on our long standing clinical and scientific expertise in mitochondrial disease. We are totally committed to provide the best of care for our patients and this means that we must understand more about the mechanisms underlying mitochondrial disease. If we are to develop new strategies for preventing or treating mitochondrial disease it is fundamentally dependent upon very high quality research.
On the background of a long history in this area we were delighted to be awarded a Wellcome Trust Centre and the significant support of the Trust and Newcastle University means that we can develop our research into new areas and potentially help more patients with mitochondrial disease.
In addition to our research strategy we are very committed to keeping patients and families fully informed of new advances in mitochondrial research and explaining the complexities of mitochondrial disease. This website is part of our initiative in this area and we want to make sure that everyone finds coming to the website helpful and informative. Over the next few years we will be developing new videos to explain mitochondrial disease and are constantly looking at new ways to explain mitochondrial disease.
One of the things we most value is the continued relationship with our patients and their supporters. Our research over the years has received invaluable help from support from both the Muscular Dystrophy Campaign and The Lily Foundation. Both are marvellous charities that help patients and families with mitochondrial disease. The whole field will only move forward by us all working together to provide better care for all patients with mitochondrial disease.
The Wellcome Trust Centre for Mitochondrial Research, based in Newcastle University, was established in May 2012 Mitochondrial Research Group with the aim of developing a seamlessly integrated programme of basic and clinical mitochondrial disease research. The Centre will not only push forward our understanding of mitochondrial disease mechanisms, but is also committed to training future generations of exceptional young researchers and to a programme of public engagement that will inform the development of its research strategy. A huge breadth of mitochondrial research is undertaken at the Wellcome Trust Centre for Mitochondrial Research, but the Centre is specifically funded to address fundamental questions regarding mitochondrial gene expression, the prevention of mitochondrial DNA disease transmission, the identification of mechanisms by which mitochondrial dysfunction causes neurological problems and the role that mitochondria play in chronic disease.
We have very close links to the NHS Highly Specialised NHS Service for Rare Mitochondrial Disorders of Adults and Children. This Clinical Service is based within the Newcastle upon Tyne Hospitals NHS Foundation Trust and provides care for patients throughout the UK both in terms of diagnosis and management. It is led by Professor Doug Turnbull for adults and Dr Robert McFarland for children. There is a diagnostic laboratory led by Professor Rob Taylor providing tests for both biochemical and genetic diagnosis.
In addition, we are developing the next generation of outstanding scientists through an innovative research training program in mitochondrial medicine and have established a new MRes course in Mitochondrial Biology and Medicine. This course, together with an array of PhD and post-doctoral training iniatives, will enable the Centre to provide world-class education and training in mitochondrial disease research to leading scientists of the future.

Public Engagement
As a Wellcome Trust Centre, we are committed to a process of public engagement that we hope will inform and develop our strategies for research and communication of research outcomes. Our work to prevent the disease passing from mothers to children involves new IVF techniques that involve a greater understanding by the public as well as discussion with key policy makers. We will develop new approaches to engage with patients and public, and guide policy development to support the use of new techniques to prevent transmission of mitochondrial DNA disease.
Our Vision
The Wellcome Trust Centre for Mitochondrial Research is an internationally recognised centre of excellence. We aim to make a major difference to the lives of patients with disease caused by mitochondrial dysfunction. We will achieve this by integrating international quality research with training excellent young scientists and engaging with policy makers, our patients and the public.

Reviews

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Please help support The Lily Foundation by joining their first ever virtual fundraising quiz night with Josh Widdicombe! See below for more information.

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The latest psychological well-being update from the Newcastle Mitochondrial Team includes advice on coping with loneliness and isolation during the ongoing coronavirus situation. To find out more: https://www.newcastle-mitochondria.com/co ronavirus-latest-…/

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Members of the WCMR clinical team have been involved in the production of new consensus statements for mitochondrial disease that are now available for professionals on our website. For more information: https://www.newcastle-mitochondria.com/‚Ä ¶/clinica‚Ķ/index.html

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The Lily Foundation have put together some useful contacts for those feeling particularly vulnerable during the coronavirus crisis. To find out more: https://www.thelilyfoundation.org.uk/…/ coronavirus-useful-…/

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You can now register for support if you have a medical condition that makes you vulnerable to coronavirus. We would urge all people affected by mitochondrial disease to register online using the following link: https://www.gov.uk/coronavirus-extremely- vulnerable

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A huge thank you to Dr Brendan Payne for hosting our first remote WCMR 'Research in Progress' meeting today. It was great to have nearly 70 members of the WCMR team join the call and ask lots of questions.

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Updated advice on coronavirus for patients and families is available here: https://www.newcastle-mitochondria.com/co ronavirus-updated…/

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Please see the latest government advice on shielding to protect from coronavirus: https://www.newcastle-mitochondria.com/co ronavirus-updated…/

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In line with government advice on coronavirus, please see the latest information for mitochondrial patients and their families: https://www.newcastle-mitochondria.com/co ronavirus-updated…/
Information can also be found on The Lily Foundation website: https://www.thelilyfoundation.org.uk/coro navirus-advice/ and the Rare Mitochondrial Disorders website: https://mitochondrialdisease.nhs.uk/…/c oronavirus-and-mito…/

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UPDATED LINKS BELOW. As usual our team are working very hard to ensure the safety of all of our patients. In addition to our patient care and support work, many of our staff will be required to help out the wider NHS community due to the ongoing coronavirus (Covid-19) situation.
During this busy time, we are unable to reply to any comments or queries made via our social media.
... For up to date government guidance on coronavirus, please see https://www.gov.uk/…/coronavirus-covid- 19-uk-government-res…. Also advice from The Lily Foundation https://www.thelilyfoundation.org.uk/coro navirus-advice/ and The Rare Mitochondrial Disorders Service https://mitochondrialdisease.nhs.uk/…/c oronavirus-and-mito…/
We hope you keep safe during this extremely difficult time. Many thanks, The Newcastle Mitochondrial Team.
See More

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The Newcastle Mitochondrial Team recognise that the ongoing coronavirus situation is causing a great deal of uncertainty and anxiety. With this in mind, we would like to share some advice on psychological and emotional wellbeing. To read more: https://www.newcastle-mitochondria.com/co ronavirus-mental-…/

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The NHS Rare Mitochondrial Disorders website has updated advice on coronavirus. To read more: https://mitochondrialdisease.nhs.uk/…/c oronavirus-and-mito…/

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In line with government advice on coronavirus, please read and follow the updated information for mitochondrial patients and their families: https://www.newcastle-mitochondria.com/co ronavirus-latest-…/

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It is with great regret that the WCMR and The Lily Foundation have decided to postpone the Patient Engagement Day due to take place on Tuesday 16th June 2020 in Newcastle as part of Euromit 2020. More information here: http://euromit2020.org/postponement

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The WCMR team have taken the decision to postpone Euromit 2020 as we have a duty of care to the entire mitochondrial community across the world. This includes patients, doctors, researchers and their families. For more information: http://euromit2020.org/postponement

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Jack Collier is a 3rd year PhD student in the WCMR who was awarded a prestigious EMBO short-term fellowship. To find out more about how this award has boosted his PhD studies, click here: https://www.newcastle-mitochondria.com/pr estigious-embo-fe…/

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In light of the ongoing coronavirus situation in the UK, the Newcastle Mitochondrial Team have put together some general advice for those affected by mitochondrial disease. Follow the link for more information: http://www.newcastle-mitochondria.com/cor onavirus-advice-f…/

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The WCMR team would like to congratulate Dr Albert Lim on his recent award from the Leigh Syndrome International Consortium!

More about Mitochondrial Research

Mitochondrial Research is located at Newcastle University, Medical School, Framlington Place, NE2 4HH Newcastle upon Tyne
0191 208 3084
Monday: 09:00 - 17:00
Tuesday: 09:00 - 17:00
Wednesday: 09:00 - 17:00
Thursday: 09:00 - 17:00
Friday: 09:00 - 17:00
Saturday: -
Sunday: -
http://www.newcastle-mitochondria.com/