Recessive Stargardt disease (STGD1) is an inherited blinding disorder caused by mutations
in the Abca4 gene. ABCA4 is a flippase in photoreceptor outer segments (OS) that …

While rods in the mammalian retina regenerate rhodopsin through a well-characterized
pathway in cells of the retinal pigment epithelium (RPE), cone visual pigments are thought to …

The high sensitivity of night vision requires that rod photoreceptors reliably and reproducibly
signal the absorption of single photons, a process that depends on tight regulation of …

Recessive Stargardt disease (STGD1) is an inherited retinopathy caused by mutations in the
ABCA4 gene. The ABCA4 protein is a phospholipid-retinoid flippase in the outer segments …

Peropsin is a non-visual opsin in both vertebrate and invertebrate species. In mammals,
peropsin is present in the apical microvilli of retinal pigment epithelial (RPE) cells. These …

RMS is a family of soft tissue tumors which is associated with skeletal muscle lineage, and it
usually occurs in the pediatric population. It is the most common sarcoma in the head and …

Paraneoplastic neurological disorder (PND) is a condition due to immune cross-reactivity
between the tumour cells and the normal tissue, whereby the “onconeural” antibodies attack …

Preschoolers’ inhibitory control and early math skills were concurrently and longitudinally
examined in 255 Chinese, African American, Dominican, and Mexican 4-year-olds in the …

Mothers' spontaneous teaching of their 4-year-olds was observed during block play in 230
dyads from low-income African American, Mexican, Dominican, and Chinese backgrounds. …

This letter presents the first case of implementing deep-learning based instrument tracking
on a magnetic anchored surgical endoscope. The compact magnetic actuated endoscope …