16.06.14

Gene therapy: a "molecular scalpel" corrects the genes of blood stem cells

A group of researchers at the San Raffaele Telethon Institute for Gene Therapy (TIGET) in Milan was able for the first time to rewrite the DNA of human blood stem cells by editing the genome.

From Research

16.06.14

Cardiomyopathies: a protein has been discovered that keeps the heart young

It's called Atrogin-1 and it's a protein that plays an important role in cardiac health: its task, as demonstrated by a study funded by Telethon, is to identify and dispose of the waste substances produced by cellular activity, which would be harmful to the heart.

From Research

10.02.14

Ipex syndrome: fresh hope for a cure from Telethon - San Raffaele researchers

From Telethon - San Raffaele research come new treatment prospects for a rare genetic diseases affecting the immune system, IPEX syndrome.

From Research

10.02.14

Towards success

Up to June 30, 2013, the Telethon Foundation has invested over € 394 million to fund 2470 research projects, which have yielded 9350 articles in international scientific journals.

From Telethon Foundation

14.01.14

From Telethon-funded gene therapy comes a new weapon in the battle against cancer

The innovative technique developed in the laboratories of the Telethon San Raffaele Institute for Gene Therapy for the treatment of two extremely serious genetic diseases can also be effective in treating tumours.

From Research

14.01.14

TIGEM: a centre of excellence for the south

The new premises of the Telethon Institute for Genetics and Medicine (Tigem) is set to open in the former "Olivetti area" in Pozzuoli.

From Research

06.11.13

Research into a rare kidney disease reveals a mechanism responsible for hypertension

Research into a rare kidney disease has shed important light on a possible way to tackle high blood pressure, a risk factor for the circulatory system that in Italy alone affects a third of the adult population.

From Research

29.10.13

Polycystic kidney: a problem of tubule expansion lies at the base of polycystic kidney disease

New light has been shed on the molecular mechanisms that lie at the base of one of the most common genetic diseases, autosomal dominant polycystic kidney, which in Italy alone affects 60 thousand people.

From Research

16.10.13

Collaboration agreement between Telethon Foundation and Rare Partners

Telethon has renewed the agreement with Rare Partners for the development of diagnostic tools and therapeutic approaches based on the results of research projects funded by the Telethon Foundation.

From Telethon Foundation

Il tuo browser non è più supportato da Microsoft, esegui l'upgrade a Microsoft Edge per visualizzare il sito.