Results 91 to 100 of about 182,280 (265)
Guimarães Editores [editorial] (Lisboa, 1899- )
Verbete dedicado a esta editora centenária, integrado na secção portuguesa do Portal Editores y Editoriales Iberoamericanos (siglos XIX XXI) - EDI-RED, o qual faz parte integrante do mega-portal Biblioteca Virtual Miguel de Cervantes, da Fundação Miguel ...
Melo, Daniel
core
Organic electrochemical transistors bridge biological ionic signaling and neuromorphic computation through volumetric electrochemical gating. This review connects Organic mixed ionic–electronic conductor materials, device architectures, and manufacturing technologies to show how geometry, ion transport, and fabrication strategies program plasticity ...
Hyunjin Lee +5 more
wiley +1 more source
Entre 1931 y 1932, como ocurrió en otras regiones españolas, Castilla y León asistió al resurgir de un regionalismo que hasta la fecha apenas había dado síntomas de vitalidad.
Luis Felipe PALACIOS
doaj
Message from the editors of the theme issueMensagem dos editores do ...
Menezes Amaral, Carlos Eduardo +2 more
core
Engineered Transformer Base Editor with Enhanced Editing Efficiency
A highly efficient transformer base editor system achieves robust genomic editing in a humanized mouse model. This work establishes a versatile and translatable platform, opening new avenues for precision gene therapy. ABSTRACT Canonical cytosine base editors (CBEs) achieve precise C‐to‐T conversions without inducing DNA double‐strand breaks (DSBs ...
Bowen Chen +5 more
wiley +1 more source
Informação e formação na área farmacêutica [PDF]
Anselmo Gomes de OLIVEIRA +1 more
doaj +1 more source
Retos pendientes y nuevas situaciones en la gestión de la propiedad intelectual
No podemos decir que la propiedad intelectual no esté de moda. Nunca se habían hecho tantos informes, cursos, estudios y publicaciones; nunca fue tan frecuente acercarse a la legislación exterior o aventurarse en nuevos enfoques para nuevas situaciones ...
Martínez Rodríguez, Emiliano
doaj
CRISPR and Gene Augmentation Rescue Trabecular Meshwork Dysfunction in iPSC Models of Lowe Syndrome
By modeling Lowe syndrome using patient‐derived iPSCs, this study establishes a human disease model that faithfully recapitulates OCRL deficiency‐associated ciliary and cytoskeletal defects. The model enables evaluation of both mutation‐agnostic DNA augmentation and CRISPR‐mediated mutation correction strategies, both of which restore OCRL function and
Siyu Chen +11 more
wiley +1 more source

