Lataa...

Genomic DNA nanoparticles rescue rhodopsin-associated retinitis pigmentosa phenotype

Mutations in the rhodopsin gene cause retinal degeneration and clinical phenotypes including retinitis pigmentosa (RP) and congenital stationary night blindness. Effective gene therapies have been difficult to develop, however, because generating precise levels of rhodopsin expression is critical; o...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:FASEB J
Päätekijät: Han, Zongchao, Banworth, Marcellus J., Makkia, Rasha, Conley, Shannon M., Al-Ubaidi, Muayyad R., Cooper, Mark J., Naash, Muna I.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Federation of American Societies for Experimental Biology 2015
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4447225/
https://ncbi.nlm.nih.gov/pubmed/25713057
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.15-270363
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!