Overview

retinal2


'retinal2' can also refer to...

retinal2

NR2E3-Linked Retinal Degenerations Enhanced S-Cone Sensitivity Syndrome, Goldmann-Favre Syndrome, Clumped Pigmentary Retinal Degeneration, and Retinitis Pigmentosa

Deficiency of pantothenate kinase 2 (Pank2) in mice leads to retinal degeneration and azoospermia

Dlx2 homeobox gene transcriptional regulation of Trkb neurotrophin receptor expression during mouse retinal development

Incidence Rates of Retinal Detachment in 2 Cohorts of Patients Treated With Oral Fluoroquinolones or Amoxicillin

CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice

KASH protein Syne-2/Nesprin-2 and SUN proteins SUN1/2 mediate nuclear migration during mammalian retinal development

Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cells

Are Retinal Microvascular Phenotypes Associated With the 1675G/A Polymorphism in the Angiotensin II Type-2 Receptor Gene?

Animals deficient in C2Orf71, an autosomal recessive retinitis pigmentosa-associated locus, develop severe early-onset retinal degeneration

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration

In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development

Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene

The Gene Responsible for Autosomal Dominant Doyne's Honeycomb Retinal Dystrophy (DHRD) Maps to Chromosome 2p16

Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice

Cytomegalovirus Infection Decreases Expression of Thrombospondin-1 and -2 in Cultured Human Retinal Glial Cells: Effects of Antiviral Agents

Aging and Dementia-2Retinal and Serum Lutein and Zeaxanthin: Relation to White Matter Integrity in Younger and Older Adults

Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors

 

More Like This

Show all results sharing this subject:

  • Chemistry

GO

Show Summary Details

Quick Reference

(sometimes) an alternative name for 3,4‐didehydroretinal(especially to distinguish it from retinal1; not recommended).

Subjects: Chemistry.


Reference entries

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.