RPE65 (Russian Wikipedia)

Analysis of information sources in references of the Wikipedia article "RPE65" in Russian language version.

refsWebsite

Global rank Russian rank

4^th place

6^th place

2^nd place

3^rd place

1^st place

low place

doi.org (Global: 2^nd place; Russian: 3^rd place)

Bowne, SJ; Humphries, M.M., Sullivan, L.S., Kenna, P.F., Tam, L.C., Kiang, A.S., Campbell, M., Weinstock, G.M., Koboldt, D.C., Ding, L., Fulton, R.S., Sodergren, E.J., Allman, D., Millington-Ward, S., Palfi, A., McKee, A., Blanton, S.H., Slifer, S., Konidari, I., Farrar, G.J., Daiger, S.P., Humphries, P. A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (англ.) // European journal of human genetics : EJHG : journal. — 2011. — 8 June (vol. 19, no. 10). — P. 1074—1081. — doi:10.1038/ejhg.2011.86. — PMID 21654732.
Bennett J., Ashtari M., Wellman J., et al. AAV2 gene therapy readministration in three adults with congenital blindness (англ.) // Sci Transl Med^[англ.] : journal. — 2012. — February (vol. 4, no. 120). — P. 120ra15. — doi:10.1126/scitranslmed.3002865. — PMID 22323828.

Hamel C.P., Tsilou E., Pfeffer B.A., Hooks J.J., Detrick B., Redmond T.M. Molecular cloning and expression of RPE65, a novel retinal pigment epithelium-specific microsomal protein that is post-transcriptionally regulated in vitro (англ.) // J Biol Chem : journal. — 1993. — August (vol. 268, no. 21). — P. 15751—15757. — PMID 8340400.
Entrez Gene: RPE65 retinal pigment epithelium-specific protein 65kDa . Архивировано 7 марта 2010 года.
Bowne, SJ; Humphries, M.M., Sullivan, L.S., Kenna, P.F., Tam, L.C., Kiang, A.S., Campbell, M., Weinstock, G.M., Koboldt, D.C., Ding, L., Fulton, R.S., Sodergren, E.J., Allman, D., Millington-Ward, S., Palfi, A., McKee, A., Blanton, S.H., Slifer, S., Konidari, I., Farrar, G.J., Daiger, S.P., Humphries, P. A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (англ.) // European journal of human genetics : EJHG : journal. — 2011. — 8 June (vol. 19, no. 10). — P. 1074—1081. — doi:10.1038/ejhg.2011.86. — PMID 21654732.
Bennett J., Ashtari M., Wellman J., et al. AAV2 gene therapy readministration in three adults with congenital blindness (англ.) // Sci Transl Med^[англ.] : journal. — 2012. — February (vol. 4, no. 120). — P. 120ra15. — doi:10.1126/scitranslmed.3002865. — PMID 22323828.

Bennett J., Ashtari M., Wellman J., et al. AAV2 gene therapy readministration in three adults with congenital blindness (англ.) // Sci Transl Med^[англ.] : journal. — 2012. — February (vol. 4, no. 120). — P. 120ra15. — doi:10.1126/scitranslmed.3002865. — PMID 22323828.