Results 151 to 160 of about 209,877 (288)
Stage-sensitive potential of isolated rabbit ICM to differentiate into extraembryonic lineages†. [PDF]
Filimonow K +8 more
europepmc +1 more source
Genome‐wide codon reprogramming of influenza A virus introduces 1956 synonymous mutations across five segments and elevates CpG content, causing defective NA packaging, loss of NS1 accumulation, and enhanced ZAP‐mediated antiviral responses without affecting RNA or protein synthesis. These mechanisms result in profound attenuation and potent homologous
Yang Wang +13 more
wiley +1 more source
The Consequences of DNA Damage in the Early Embryo Are Important for Practical Procedures in Assisted Reproduction. [PDF]
Baran V, Čikoš Š, Fabian D.
europepmc +1 more source
Immunoisolation of centrosomes from Drosophila melanogaster [PDF]
Lange, B., Lehmann, V., Müller, H.
core +2 more sources
HUWE1 in Skeletal Muscle Prevents Muscle Fatigue via Maintaining Iron and Calcium Homeostasis
This study investigates the impact of iron homeostasis on exercise. Loss of the HECT domain‐containing ubiquitin ligase E3 (HUWE1) in skeletal muscle restrains the exercise performance in mice with downregulated ferroportin expression leading to iron overload, which is ameliorated by dietary iron restriction.
Huike Jiao +10 more
wiley +1 more source
Dynamic Remodeling of the Zona Pellucida: Implications for Oocyte Competence and Assisted Reproduction. [PDF]
de la Fuente D +8 more
europepmc +1 more source
Osteoclast‐Derived SLIT3 Mediates Osteoarthritis Pain and Degenerative Changes
In TMJ‐OA, osteoclasts play a significant role in promoting the growth of sensory nerves at the osteochondral interface. In early OA, TRAP+ osteoclast‐derived SLIT3 induces sensory nerve growth into the condylar cartilage. This nerve growth facilitates the development of pain associated with OA.
Weiwei Zhu +13 more
wiley +1 more source
Amplification of Ultra-Trace DNA from Early Sheep Embryos Based on qPCR: Establishing a Gender Identification System. [PDF]
Niu P +7 more
europepmc +1 more source
ABSTRACT Spondylocostal dysostosis (SCDO) is a rare genetic disorder characterized by abnormal development of the axial skeleton, resulting in malformations of the vertebrae and ribs that often impair lung development and lead to significant respiratory morbidity.
Jonathan Rips +8 more
wiley +1 more source

