Results 191 to 200 of about 6,410,352 (379)
Format-Preserving Encryption: Image Encryption Under FF1 Scheme
We also acknowledge institutional support from the Unit of Information Resources for Research at the “Consejo Superior de Investigaciones Científicas” (CSIC) for the article‐processing charges contribution.
Rodríguez César, Hadrian +3 more
openaire +1 more source
Nuclear pore links Fob1‐dependent rDNA damage relocation to lifespan control
Damaged rDNA accumulates at a specific perinuclear interface that couples nucleolar escape with nuclear envelope association. Nuclear pores at this site help inhibit Fob1‐induced rDNA instability. This spatial organization of damage handling supports a functional link between nuclear architecture, rDNA stability, and replicative lifespan in yeast.
Yamato Okada +5 more
wiley +1 more source
An efficient image encryption scheme based on Lorenz system and quantum-inspired walks. [PDF]
Karmany M +4 more
europepmc +1 more source
IMAGE ENCRYPTION USING CHAOTIC MAPS OF VARIOUS DIMENSIONS: REVIEW
Rekha Raj .
openalex +1 more source
openaire +1 more source
Erythropoietin administration suppresses hepatic soluble epoxide hydrolase (sEH) expression, leading to increased CYP‐derived epoxides. This is associated with a shift in hepatic macrophage polarization characterized by reduced M1 markers and increased M2 markers, along with reduced hepatic inflammation, suppressed hepatic lipogenesis, and attenuated ...
Takeshi Goda +12 more
wiley +1 more source
An optimized novel lightweight block cipher for image encryption. [PDF]
Mohanapriya R, Nithish KV.
europepmc +1 more source
Advanced Partial Image Encryption using Two-Stage Hill Cipher Technique
Panduranga HT, Naveen Kumar S K
openalex +1 more source
A new image encryption scheme based on coupling map lattices with mixed multi-chaos [PDF]
Xingyuan Wang +4 more
openalex +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source

