Results 261 to 270 of about 165,368 (343)
Developmental Characterization of the Choroid Plexus in Sialidosis (Neu1 Deficient) Mice
Danielle Helton
openalex +1 more source
The conversion of lactate to lactyl‐CoA facilitates enzymatic histone lactylation, transforming glycolytic by‐products into an epigenetic regulatory mechanism for gene expression. Lactylation modification influences macrophage polarization towards M1 or M2 phenotypes, affecting outcomes in infection, cancer and fibrosis. Targeting lactylation modifiers
Houhua Guo +5 more
wiley +1 more source
ABSTRACT Background Cerebral perivascular spaces (PVS) are involved in cerebrospinal fluid (CSF) circulation and clearance of metabolic waste in adult humans. A high number of PVS has been reported in autism spectrum disorder (ASD) but its relationship with CSF and disease severity is unclear.
Giulia Frigerio +8 more
wiley +1 more source
Axial Length Profiles in Inherited Retinal Diseases-A Genotypic and Phenotypic Analysis. [PDF]
Zhang L +8 more
europepmc +1 more source
Cystoid macular edema in gyrate atrophy of choroid and retina associated with hyperornithinemia
Martina Galiot Delić +5 more
openalex +2 more sources
RPE‐targeted gene therapy restored melanin expression and relieved ocular dysfunction. By optimizing the injection method, a wider range of melanin expression and better therapeutic effects have been achieved. ABSTRACT Oculocutaneous albinism (OCA) represents a genetically heterogeneous autosomal recessive condition marked by reduced melanin production
Li Song +18 more
wiley +1 more source
The Influence of Highly Aspherical Lenslets on Choroidal Thickness and Axial Length. [PDF]
Paulasto L, Carré C, Loertscher M.
europepmc +1 more source

