El déficit de alfa-1 antitripsina es una enfermedad rara hereditaria que predispone al desarrollo de enfisema pulmonar y diversas patologías hepáticas como la cirrosis y el hepatocarcinoma
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The Centre for Genomic Regulation (CRG) in Barcelona has secured five highly competitive doctoral fellowships from ”la Caixa” Foundation’s INPhINIT programme.
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Results of a VHIO led study show that up to 90% of chronically hypoxic patients have an EPAS1 alteration in their tumor, a gene critical for adapting to lack of oxygen in populations living at high-al...
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This discovery could facilitate earlier diagnosis in children and also help slow the effects of the syndrome from its earliest stages, significantly improving patients' quality of life.
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A CNIC team has developed an innovative gene therapy strategy for arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5), a rare and deadly inherited condition that particularly affects young ...
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La inhibición de una proteína clave en la señalización del crecimiento celular bloquea la progresión tumoral en el adenocarcinoma de pulmón, según un estudio liderado por el CSIC
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Each tumour is unique, and predicting the therapeutic response to non-small cell lung cancer is a breakthrough in personalized medicine. Given this challenge in biomedicine, the study confirms that th...
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The work identifies variants in genes such as NFU1 that, combined with the disease-causing mutation, can accelerate kidney deterioration. familial hypomagnesaemia with hypercalciuria and nephrocalcin...
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A scientific team at IRB Barcelona has, for the first time, described which hybrid triplexes (DNA-RNA) are most stable within the cell and how they are distributed throughout the human genome.
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Los investigadores han inhibido una proteína llamada ELOVL6, presente en la membrana plasmática de las células, lo que hace que pierda su función y se altere su rigidez y permeabilidad. Esta acci...
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This syndrome is the one that has received the financial donation from Cellers Maset, that through the Pau Massana scholarship collaborates annually with the Parc Taulí Research and Innovation Instit...
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A team from the Sant Pau Research Institute (IR Sant Pau), in collaboration with the Catalan Down Syndrome Foundation, has published in the journal Annals of Neurology the largest study to date on bra...
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La mejor actitud que podemos adoptar es la de trat...
The research team observed changes in head circumf...
AtCDF3 gene induced greater production of sugars a...
En nuestro post hablamos sobre este interesante tipo de célula del...
Telum Therapeutics, a biotechnology company leveraging proprietary met...
