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genetics

Centre for Personalised Medicine

Extra - 2023-24: the year in review

We discuss the highlights for the CPM in 2023-24, and look forward to the next year.
A Good Science Read

A Good Science Read: On the Origin of Modern Humans

Professor Chris Miller and Professor Frances Ashcroft discuss 'Who We Are and How We Got Here' by the Harvard geneticist David Reich.
Centre for Personalised Medicine

Series 2 Episode 7 - Why research regulation falls short in genomic medicine

As a society, we tend to focus a lot on risk and try to control it through regulation - but how well does that work for ensuring ethical practice in genomics? We talk to Dr Kate Lyle about her research on this topic.
Centre for Personalised Medicine

Series 2 Episode 3 - Sharing genetic results within families

Who does a genetic result belong to? What might help people to share genetic information with their relatives? We talk to Lisa Ballard and Anneke Lucassen.
Centre for Personalised Medicine

Series 2 Episode 2 - Why context matters in genetic testing

How can the same genetic finding can mean different things in different people? What does this mean for 'personalising' genetic results? Anneke Lucassen talks to us about this issue.
Families for the Treatment of Hereditary Motor Neuron Disease

The Future of Treating Genetic MND

Professor Kevin Talbot, University of Oxford, gives the fifth and final talk in the day's event, looking at the future of genetic MND and what the future holds for it.
Wolfson College Podcasts

The Quest for the Structure of the Ribosome: A Personal Voyage

The 2019 Haldane Lecture was delivered by Sir Venki Ramakrishnan, President of the Royal Society, on February 7th at Wolfson College, Oxford. The lecture was introduced by College President Sir Tim Hitchens.
Surgical Grand Rounds Lectures

The 100,000 Genomes Project

Ms Jennifer Whitfield talks about the 100,000 Genomes Project, which aims to establish a new genomic medicine service through the NHS by sequencing the entire genomes of around 70,000 people with rare inherited diseases or cancer.
Journey of a Molecular Detective; David Sherratt

Epigenetics: Environment, embodiment and equality

Rebecca Richmond gives a talk for the UBVO seminar series on 13th October 2016.
Journey of a Molecular Detective; David Sherratt

Tracking infections

Professor Derrick Crook from our Experimental Medicine division tells us about his research on tracking infections
Journey of a Molecular Detective; David Sherratt

Tracking infections

Professor Derrick Crook from our Experimental Medicine division tells us about his research on tracking infections
Wellcome Trust Centre for Human Genetics

Method in the Motion

A unique evening combining a scientific talk with inspirational dance.
Journey of a Molecular Detective; David Sherratt

How can massive genetic studies help us prevent and treat diabetes?

Any pair of individuals will share 99.9% of their DNA. But that 0.1% difference can tell us a huge amount about the causes of disease and how we can treat them. Find out more about the genetics that underpin type 2 diabetes.
The Secrets of Mathematics

Modelling genes: the backwards and forwards of mathematical population genetics - Alison Etheridge

In this lecture Professor Alison Etheridge explores some of the simple mathematical caricatures that underpin our understanding of modern genetic data.
Anthropology

Inflammaging and its role in ageing and age-related diseases

Cristina Giuliani (Bologna) places inflammaging, and genetics, within an evolutionary perspective. A medical anthropology seminar given on 1 February 2016.
Journey of a Molecular Detective; David Sherratt

Governing Plastic Biology: Biopolitics in Epigenetic Times.

Maurizio Meloni, University of Sheffield, gives a talk for the UBVO seminar series.
Journey of a Molecular Detective; David Sherratt

Rare neurological disorders

Chorea-Acanthocytosis: ChAc is a rare progressive neurological disorder caused by mutations in a very complex gene.
Genetics

Rare neurological disorders

Chorea-Acanthocytosis: ChAc is a rare progressive neurological disorder caused by mutations in a very complex gene.
Journey of a Molecular Detective; David Sherratt

Computation and genetics

Resistance to drugs in bacteria can be aquired by swapping genes between individual bacteria. Computer programs developed by Dr Iqbal enable doctors to predict which antibiotics will be met with drug resistance, enabling the selection of the right drug.
Genetics

Computation and genetics

Resistance to drugs in bacteria can be aquired by swapping genes between individual bacteria. Computer programs developed by Dr Iqbal enable doctors to predict which antibiotics will be met with drug resistance, enabling the selection of the right drug.

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