<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8</volume><submitter>Chalmel F</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Cone degeneration is the hallmark of the inherited retinal disease retinitis pigmentosa. We have previously identified a trophic factor "Rod-derived Cone Viability Factor (RdCVF) that is secreted by rods and promote cone viability in a mouse model of the disease.&lt;h4>Results&lt;/h4>Here we report the bioinformatic identification and the experimental analysis of RdCVF2, a second trophic factor belonging to the Rod-derived Cone Viability Factor family. The mouse RdCVF gene is known to be bifunctional, encoding both a long thioredoxin-like isoform (RdCVF-L) and a short isoform with trophic cone photoreceptor viability activity (RdCVF-S). RdCVF2 shares many similarities with RdCVF in terms of gene structure, expression in a rod-dependent manner and protein 3D structure. Furtherm</pubmed_abstract><journal>BMC molecular biology</journal><pagination>74</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2064930</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Rod-derived Cone Viability Factor-2 is a novel bifunctional-thioredoxin-like protein with therapeutic potential.</pubmed_title><pmcid>PMC2064930</pmcid><pubmed_authors>Chalmel F</pubmed_authors><pubmed_authors>Sahel JA</pubmed_authors><pubmed_authors>Berdugo N</pubmed_authors><pubmed_authors>Leveillard T</pubmed_authors><pubmed_authors>Morel E</pubmed_authors><pubmed_authors>Lardenois A</pubmed_authors><pubmed_authors>Jaillard C</pubmed_authors><pubmed_authors>Koehl P</pubmed_authors><pubmed_authors>Lambrou G</pubmed_authors><pubmed_authors>Poch O</pubmed_authors><pubmed_authors>Holmgren A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rod-derived Cone Viability Factor-2 is a novel bifunctional-thioredoxin-like protein with therapeutic potential.</name><description>&lt;h4>Background&lt;/h4>Cone degeneration is the hallmark of the inherited retinal disease retinitis pigmentosa. We have previously identified a trophic factor "Rod-derived Cone Viability Factor (RdCVF) that is secreted by rods and promote cone viability in a mouse model of the disease.&lt;h4>Results&lt;/h4>Here we report the bioinformatic identification and the experimental analysis of RdCVF2, a second trophic factor belonging to the Rod-derived Cone Viability Factor family. The mouse RdCVF gene is known to be bifunctional, encoding both a long thioredoxin-like isoform (RdCVF-L) and a short isoform with trophic cone photoreceptor viability activity (RdCVF-S). RdCVF2 shares many similarities with RdCVF in terms of gene structure, expression in a rod-dependent manner and protein 3D structure. Furtherm</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Aug</publication><modification>2026-05-05T04:30:26.92Z</modification><creation>2026-04-07T21:21:45.109Z</creation></dates><accession>S-EPMC2064930</accession><cross_references><pubmed>17764561</pubmed><doi>10.1186/1471-2199-8-74</doi></cross_references></HashMap>