Results 161 to 170 of about 640,739 (357)
Peripheral retinal degeneration.
British Journal of Ophthalmology, 2020 H. Yaoeda
semanticscholar +1 more source
Corticospinal Tract Development, Evolution, and Skilled Movements
Movement Disorders, EarlyView.Abstract The evolution of the corticospinal tract (CST) is closely linked to the development of skilled voluntary movements in mammals. The main evolutionary divergence concerns the position of the CST within the spinal cord white matter and its postsynaptic targets in the grey matter.
Emmanuel Roze +2 more
wiley +1 more source
Retinal vascular architecture is maintained in retinal degeneration: corrosion cast and electron microscope study [PDF]
, 2001 Imran Ahmed Bhutto, Tsugio Amemiya
openalex +1 more source
Current Advances in the Combination of Fatty Acids and Resveratrol to Fight Ocular Diseases
Molecular Nutrition &Food Research, EarlyView.Graphical abstract illustrating the effects of Resvega administration on choroidal neovascularization and resveratrol metabolism in the retina. The diagram illustrates that oral administration of Resvega leads to a decrease in choroidal neovascularization.
Dominique Delmas +3 more
wiley +1 more source
Molecular Nutrition &Food Research, EarlyView.(Poly)phenols constitute a source of natural therapeutic molecules capable of targeting angiogenesis in different scenarios. This review summarizes the current evidence of the role of (poly)phenols in modulating angiogenesis. The reader can find a compilation of preclinical and human investigations describing pro‐ and anti‐angiogenic effects of these ...
María Ángeles Ávila‐Gálvez +5 more
wiley +1 more source
A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation (Pdebrd1) in FVB/N-derived transgenic mice [PDF]
, 2001 Estela Giménez, Lluı́s Montoliu
openalex +1 more source
RETINAL DEGENERATION IN HEREDITARY ATAXIA [PDF]
Journal of Neurology, Neurosurgery & Psychiatry, 1956 L. Wadensten, U. Lindblom, Å. Björk
openaire +3 more sources
The Journal of Pathology, EarlyView.Abstract Variants in the CNGB3 gene, encoding the B3‐subunit of the cone photoreceptor cyclic nucleotide gated channel, are a major cause of autosomal recessive achromatopsia, a rare inherited retinal disease. The mutation spectrum of achromatopsia‐associated CNGB3 variants comprises all types of mutations, including those that are straightforward to ...
Katharina Rawnsley +3 more
wiley +1 more source