SpliceBio closes a $135 million Series B round led by EQT Life Sciences and Sanofi Ventures. Participants include Ysios and Asabys, among others

by Ysios Capital

The funding will be used to advance the clinical development of SpliceBio’s lead gene therapy candidate, SB-007 for Stargardt disease, including the ongoing interventional Phase 1/2 ASTRA study and ...

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Potential targets are identified for preventive cancer vaccines in Lynch syndrome

by Fundació Clínic per a la Recerca Biomèdica

It has been identified 24 neopeptides that could be good targets for designing preventive cancer vaccines in people with Lynch syndrome. The results show that the selected peptides are repeated among ...

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An international study led by CIC bioGUNE identifies key mechanisms of an enzyme involved in a rare metabolic disease

by CIC bioGUNE

The research, published in The FEBS Journal, improves understanding of classical homocystinuria, a hereditary metabolic disorder, and proposes new potential therapeutic approaches.

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Bioinformatics team drives significant improvements in hereditary cancer prevention and treatment

by IDIBELL - Institut d’Investigació Biomèdica de Bellvitge

A team of bioinformatics specialists from IDIBELL-ICO have identified ClinCNV and GATK-gCNV as the two most accurate current bioinformatics tools in the detection of a certain type of variants related...

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ORYZON receives European Medicines Agency approval to initiate a Phase Ib study of iadademstat in sickle cell disease

by Oryzon Genomics

Oryzon Genomics, a clinical-stage biopharmaceutical company and a European leader in epigenetics, today announced that the European Medicines Agency (EMA) has approved its Clinical Trial Application (...

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A multicenter study identifies the differentiated risk of colorectal cancer depending on the affected gene in Lynch syndrome

by Fundació Clínic per a la Recerca Biomèdica

Researchers from Clínic-IDIBAPS, within the framework of the Clínic Barcelona Comprehensive Cancer Center, have led a study analyzing how genetic mutations associated with Lynch syndrome influence t...

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IMPaCT-GENóMICA logra mejorar notablemente la tasa de diagnóstico genético

by Professional Newco

IMPaCT-GENóMICA realiza la secuenciación del genoma completo a las personas que acceden al programa tras no haber obtenido el diagnóstico con las pruebas asistenciales habituales. Con herramientas ...

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The MOSCAT Project Identifies a Hereditary Cardiac Cause in 9.5% of Sudden Deaths in Individuals Aged 35 and Under

by IdiBGi

The results, recently published, provide a practical guide for forensic doctors and cardiologists to determine when post-mortem genetic testing is most appropriate.

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A lipid metabolism enzyme is revealed as a new way to raise levels of the key protein in spinal muscular atrophy

by IRB Lleida. Institut de Recerca Biomèdica

It has been identified a biological target for combating spinal muscular atrophy: acid sphingomyelinase (ASM), an enzyme involved in the metabolism of lipids in the nervous system. Blocking its activi...

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El síndrome de Lynch también se asocia a un mayor riesgo de cáncer de páncreas y de vías biliares

by Professional Newco

Un estudio multicéntrico ha demostrado que las personas con síndrome de Lynch presentan un riesgo significativamente mayor de desarrollar cáncer de páncreas y colangiocarcinoma (cáncer de las ví...

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ORYZON announces First‑Patient‑In (FPI) in RESTORE Phase Ib trial of iadademstat in sickle cell disease

by Oryzon Genomics

Recently approved by the European Medicines Agency, RESTORE will evaluate iadademstat’s ability to raise fetal hemoglobin (HbF) in adult patients with SCD

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A new technique helps detect hidden heart problems and improve their localisation

by Universitat Politècnica de València

En sus estudios, publicados en la revista científica Heart Rhythm, presenta la métrica Vector Field Heterogeneity (VFH), presentan un nuevo indicador diseñado para cuantificar las heterogeneidades ...

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