PHG Foundation | January 2010

  PHG Foundation genomics and policy news
    14 January 2010
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Genomic medicine
We were disappointed with the UK Government’s response to the House of Lords report on Genomic Medicine (15 December); fortunately we are working with the University of Cambridge Cente for Science and Policy in a consultation process with key experts to produce an independent  response with detailed and constructive recommendations for UK health services.

Policy and regulation
In other policy news, we reported on new tools for using evidence to inform policy making (12 January), a new code of conduct for artificial gene synthesis from the International Association of Synthetic Biology (15 December), a critique of the current intellectual property system for science (17 December), and new guidance for UK researchers on the use of human tissue, DNA, and the changing regulatory and governance environment for research (6 January).

Stem cell research and policy
In stem cell research, a new toolkit aims to guide scientists through the regulatory framework in the UK (4 January), and we reported on developments in the US, India and Italy (21 December). A new technique for the genetic manipulation of human embryonic stem cells could help create more effective model disease systems (13 January).

Cancer genomics
Efforts to catalogue different cancer genomes are helping to identify mutations (18 December), and a new study of structural changes in breast cancer cells has found that tandem duplications are the most common form of rearrangement (11 January).

Genetic disease susceptibility
The first report of the human prion disease vCJD in an individual without the susceptibility genotype raises questions about the future number of cases (5 January); we also reported on new evidence for genetic susceptibility to leprosy (8 January) and of a link between G6PD deficiency and protection from malaria infection (22 December).

New reviews and commentaries
Our selection of recent articles of interest (3 January)

Other recent news and research
Gene for devastating kidney disease discovered
Stem cells likely to help genetic disorders first
The human genome ten years on: time to take stock
New genotyping chip for personalised medicine
New gene linked to congenital heart defects
Schizophrenic mouse developed
Study blames two genes for aggressive brain cancer
Gene therapy holds promise for emphysema
Discovery of new inherited eye disease
Responses to consultation on the additional uses of patient data
Genetic link to heart failure
Lack of racial and genetic diversity in stem cell lines used for research
Doctors and scientists back petition to demand reform of England's libel laws
Korean government launches disease genome research
Gene module identified in atherosclerosis
Study identifies genetic predeterminants for diabetes in African-Americans
Indian gene experts pave way for future medicines

See also the Genomics & Health Weekly Update from the CDC Office of Public Health Genomics and the GenInfo Monthly Newsletter from HumGen.

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Created: 16 February 2010