Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

NRL^-/- gene edited human embryonic stem cells generate rod-deficient retinal organoids enriched in S-cone-like photoreceptors.

Autor: Cuevas, Elisa, Holder, Daniel L., Alshehri, Ashwak H., Tréguier, Julie, Lakowski, Jörn, Sowden, Jane C.

Publikováno v: Stem Cells; Apr2021, Vol. 39 Issue 4, p414-428, 15p

NRL−/−gene edited human embryonic stem cells generate rod‐deficient retinal organoids enriched in S‐cone‐like photoreceptors

Autor: Cuevas, Elisa, Holder, Daniel L., Alshehri, Ashwak H., Tréguier, Julie, Lakowski, Jörn, Sowden, Jane C.

Publikováno v: Stem Cells; April 2021, Vol. 39 Issue: 4 p414-428, 15p

Mutation of SALL2 causes recessive ocular coloboma in humans and mice

Autor: Kelberman, Daniel, Islam, Lily, Lakowski, Jörn, Bacchelli, Chiara, Chanudet, Estelle, Lescai, Francesco, Patel, Aara, Stupka, Elia, Buck, Anja, Wolf, Stephan, Beales, Philip L, Jacques, Thomas S, Bitner-Glindzicz, Maria, Liasis, Alki, Lehmann, Ordan J, Kohlhase, Jürgen, Nischal, Ken K, Sowden, Jane C

Publikováno v: Kelberman, D, Islam, L, Lakowski, J, Bacchelli, C, Chanudet, E, Lescai, F, Patel, A, Stupka, E, Buck, A, Wolf, S, Beales, P L, Jacques, T S, Bitner-Glindzicz, M, Liasis, A, Lehmann, O J, Kohlhase, J, Nischal, K K & Sowden, J C 2014, ' Mutation of SALL2 causes recessive ocular coloboma in humans and mice ', Human Molecular Genetics, vol. 23, no. 10, ddt643, pp. 2511-2526 . https://doi.org/10.1093/hmg/ddt643
Kelberman, D, Islam, L, Lakowski, J, Bacchelli, C, Chanudet, E, Lescai, F, Patel, A, Stupka, E, Buck, A, Wolf, S, Beales, P L, Jacques, T S, Bitner-Glindzicz, M, Liasis, A, Lehmann, O J, Kohlhase, J, Nischal, K K & Sowden, J C 2014, ' Mutation of SALL2 causes recessive ocular coloboma in humans and mice ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddt643

Ocular coloboma is a congenital defect resulting from failure of normal closure of the optic fissure during embryonic eye development. This birth defect causes childhood blindness worldwide, yet the genetic etiology is poorly understood. Here, we ide

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::50ee864e4bdcfc953c8575a8c102ab32
https://pure.au.dk/portal/da/publications/mutation-of-sall2-causes-recessive-ocular-coloboma-in-humans-and-mice(95c230fa-efe8-4211-ada6-b639b88e61e8).html