Cone inputs to murine striate cortex

por Ekesten, Björn, Gouras, Peter
Publicado 2008

Corneal cross-linking in 9 horses with ulcerative keratitis

por Hellander-Edman, Anna, Makdoumi, Karim, Mortensen, Jes, Ekesten, Björn
Publicado 2013

The refractive state of the eye in Icelandic horses with the Silver mutation

por Johansson, Maria K., Jäderkvist Fegraeus, Kim, Lindgren, Gabriella, Ekesten, Björn
Publicado 2017

Erratum to: The refractive state of the eye in Icelandic horses with the Silver mutation

por Johansson, Maria K., Fegraeus, Kim Jäderkvist, Lindgren, Gabriella, Ekesten, Björn
Publicado 2017

Multiple congenital ocular anomalies in Icelandic horses

por Andersson, Lisa S, Axelsson, Jeanette, Dubielzig, Richard R, Lindgren, Gabriella, Ekesten, Björn
Publicado 2011

Abnormal Appearance of the Area Centralis in Labrador Retrievers With an ABCA4 Loss-of-function Mutation

por Ekesten, Björn, Mäkeläinen, Suvi, Ellis, Stuart, Kjellström, Ulrika, Bergström, Tomas F.
Publicado 2022

Equine Multiple Congenital Ocular Anomalies and Silver Coat Colour Result from the Pleiotropic Effects of Mutant PMEL

por Andersson, Lisa S., Wilbe, Maria, Viluma, Agnese, Cothran, Gus, Ekesten, Björn, Ewart, Susan, Lindgren, Gabriella
Publicado 2013

Effects of achromatic and chromatic lights on pupillary response, endocrinology, activity, and milk production in dairy cows

por Lindkvist, Sofia, Ternman, Emma, Ferneborg, Sabine, Bånkestad, Daniel, Lindqvist, Johan, Ekesten, Björn, Agenäs, Sigrid
Publicado 2021

Targeted analysis of four breeds narrows equine Multiple Congenital Ocular Anomalies locus to 208 kilobases

por Andersson, Lisa S., Lyberg, Katarina, Cothran, Gus, Ramsey, David T., Juras, Rytis, Mikko, Sofia, Ekesten, Björn, Ewart, Susan, Lindgren, Gabriella
Publicado 2011

Deletion in the Bardet–Biedl Syndrome Gene TTC8 Results in a Syndromic Retinal Degeneration in Dogs

por Mäkeläinen, Suvi, Hellsand, Minas, van der Heiden, Anna Darlene, Andersson, Elina, Thorsson, Elina, S. Holst, Bodil, Häggström, Jens, Ljungvall, Ingrid, Mellersh, Cathryn, Hallböök, Finn, Andersson, Göran, Ekesten, Björn, Bergström, Tomas F.
Publicado 2020

An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease

por Mäkeläinen, Suvi, Gòdia, Marta, Hellsand, Minas, Viluma, Agnese, Hahn, Daniela, Makdoumi, Karim, Zeiss, Caroline J., Mellersh, Cathryn, Ricketts, Sally L., Narfström, Kristina, Hallböök, Finn, Ekesten, Björn, Andersson, Göran, Bergström, Tomas F.
Publicado 2019

Inactivation of Pmel Alters Melanosome Shape But Has Only a Subtle Effect on Visible Pigmentation

por Hellström, Anders R., Watt, Brenda, Fard, Shahrzad Shirazi, Tenza, Danièle, Mannström, Paula, Narfström, Kristina, Ekesten, Björn, Ito, Shosuke, Wakamatsu, Kazumasa, Larsson, Jimmy, Ulfendahl, Mats, Kullander, Klas, Raposo, Graça, Kerje, Susanne, Hallböök, Finn, Marks, Michael S., Andersson, Leif
Publicado 2011