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1 天
Data and Safety Monitoring Board Approves Initiation of Phase 2 of OCU410ST GARDian ...
Determined the high dose of OCU410ST to be the maximum tolerated doseNo serious adverse events have been reportedApproved ...
modernretina
3 天
AAO 2024: Deuterated vitamin A preserves vision in Stargardt disease
Christine N. Kay, MD, discussed her presentation, "Deuterated vitamin A preserves vision in Stargardt’s disease (TEASE study) ...
4 天
Archie Hare from Richmond Dales ASC beat 100m swim record
At just 16 years old, Archie Hare, a fiercely competitive and sport-mad teenager from North Yorkshire, is making headlines in the world ...
Science Daily
6 天
Analysis of retinal proteins identifies new drug targets for treating inherited retinal ...
Researchers have identified new drug targets for therapies that could benefit patients with different forms of retinitis ...
7 天
Analysis of proteins identifies new drug targets for treating inherited retinal degenerations
An international team of researchers has identified new drug targets for therapies that could benefit patients with different ...
Le Lézard
9 天
PharmAbcine Announces Safety Approval for 4mg Single-dose Cohort in Phase 1 Clinical Trial ...
PharmAbcine, Inc. (KOSDAQ: 208340), a clinical-stage public company developing next-generation therapeutics to address unmet medical needs, ...
10 天
Belite Bio Announces Presentations at the American Academy of Ophthalmology 2024 Annual Meeting
Therefore, Belite Bio is evaluating safety and efficacy of Tinlarebant in GA patients in a 2-year Phase 3 study (PHOENIX). Belite Bio is a clinical-stage biopharmaceutical drug development company ...
11 天
Understanding Leber's Congenital Amaurosis: A Rare Genetic Eye Disorder
Leber's congenital amaurosis is a rare genetic disease caused by mutations in genes. Frida Bollani Magoni, daughter of ...
Newport Beach Independent
12 天
Set Your Sights on a True-Life Tale with ‘The Blind Sea’ at Newport Beach Film Festival
By age five, only a blurry and distorted three percent of Matt Formston’s vision remained. Despite this Australian athlete’s ...
GEN
13 天
Hubble Therapeutics Taps Andelyn to Manufacture Clinical Grade AAV for Eye Disorder Gene ...
LCA16 is a retinal dystrophy resulting from a genetic mutation which expresses a critical ion channel in retinal pigment epithelium cells.
14 天
ST takes a closer look at 4 rare eye diseases affecting children to mark World Sight Day
World Sight Day aims to raise awareness of vision impairment and blindness, and promote eye care. Read more at ...
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