Una variante genética protege del alzhéimer de aparición tardía asociado a APOE4

by Revista Genética Médica

La mutación Christchurch, que protege de la enfermedad de Alzheimer familiar causada por mutaciones en el gen PSEN1, también protege del efecto negativo de la variante APOE4, principal factor de rie...

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Glycobasque 6: A successful convergence of leading minds in glycoscience

by CIC bioGUNE

Professionals, experts, and researchers across diverse glycoscience disciplines, encompassing glycobiology, immunology, and carbohydrate chemistry, converge at the 6th edition of Glycobasque.

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New research to develop treatment for ultrarare disease caused by ADSL gene mutation

by Universitat Autònoma de Barcelona (UAB)

The UAB has launched a new campaign to raise funds to study a gene therapy for adenylsuccinate lyase deficiency (ADSL), a rare genetic disease suffered by about 80 children in the world, including two...

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Vall d'Hebron participates in clinical trial to test a new gene therapy in patients with severe combined immunodeficiency

by Vall d’Hebron

The project RECOMB, in which Vall d'Hebron participates, has recently launched a clinical trial to develop a gene therapy to cure patients with SCID, popularly known as "bubble child syndrome" who hav...

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Global trends in digital therapies

by Instituto de Investigación e Innovación Parc Taulí

The Spanish Agency for Medicines and Health Products (AEMPS) defines them advanced therapies as medicines for human use that may be based on genes (gene therapy), cells (cellular therapy) or fabrics (...

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The Ministry of Science and Innovation awards more than 6 million euros to 46 projects led by University researchers

by Universidad de Navarra

The Ministry of Science and Innovation has awarded more than 6 million euros to 46 projects led by researchers from the University of Navarra, corresponding to different areas of knowledge.

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Investigadores del Cima y de la Clínica reciben cerca de 5 millones del Ministerio de Ciencia e Innovación para 27 proyectos científicos

by CIMA - Centro de Investigación Médica Aplicada

El Ministerio de Ciencia e Innovación ha concedido cerca de 5 millones de euros a 27 proyectos liderados por investigadores de la Clínica Universidad de Navarra y del Cima para la lucha contra el cÃ...

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Vall d'Hebron receives 2.6 million euros for research into advanced therapies

by Vall d’Hebron

CERTERA's objective is to create a coordinated research and innovation structure to accelerate the preclinical and early stage clinical development of these types of therapies.

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SparingVision Reaches Final Dose Escalation Step in PRODYGY Trial with SPVN06 for retinitis pigmentosa

by Ysios Capital

SparingVision today announces a key advancement in its Phase I/II clinical trial for SPVN06, the Company’s lead gene-agnostic investigational gene therapy for the treatment of retinitis pigmentosa (...

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New therapeutic approach to treat retinitis pigmentosa and other serious eye diseases

by Fundació Bosch i Gimpera

Researchers at the University of Barcelona are participating in a new consortium to design a drug with an innovative approach against this disease, which could also be used to treat other hereditary r...

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Seis niños con sordera hereditaria mejoran la audición gracias a la terapia génica

by Revista Genética Médica

Dos recientes estudios ofrecen importantes avances en la utilización de terapia génica como tratamiento para la pérdida auditiva.

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Vivet Therapeutics receives EUR 4.9 million to advance development of a gene therapy

by Ysios Capital

Vivet Therapeutics announces the financing of EUR 4.9 million received from the French government to advance the development of a gene therapy for the treatment of cerebrotendinous xanthomatosis (CTX)...

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