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A Dpagt1 Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice.
Published in:
International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 12005, doi. 10.3390/ijms231912005
By:
- Hyde, Lillian F.;
- Kong, Yang;
- Zhao, Lihong;
- Rao, Sriganesh Ramachandra;
- Wang, Jieping;
- Stone, Lisa;
- Njaa, Andrew;
- Collin, Gayle B.;
- Krebs, Mark P.;
- Chang, Bo;
- Fliesler, Steven J.;
- Nishina, Patsy M.;
- Naggert, Jürgen K.
Publication type:
Article
A Splicing Mutation in Slc4a5 Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction.
Published in:
International Journal of Molecular Sciences, 2022, v. 23, n. 4, p. 2220, doi. 10.3390/ijms23042220
By:
- Collin, Gayle B.;
- Shi, Lanying;
- Yu, Minzhong;
- Akturk, Nurten;
- Charette, Jeremy R.;
- Hyde, Lillian F.;
- Weatherly, Sonia M.;
- Pera, Martin F.;
- Naggert, Jürgen K.;
- Peachey, Neal S.;
- Nishina, Patsy M.;
- Krebs, Mark P.
Publication type:
Article
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.
Published in:
Cells (2073-4409), 2020, v. 9, n. 4, p. 931, doi. 10.3390/cells9040931
By:
- Collin, Gayle B.;
- Gogna, Navdeep;
- Chang, Bo;
- Damkham, Nattaya;
- Pinkney, Jai;
- Hyde, Lillian F.;
- Stone, Lisa;
- Naggert, Jürgen K.;
- Nishina, Patsy M.;
- Krebs, Mark P.
Publication type:
Article
Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1<sup>rd8</sup> mouse model.
Published in:
PLoS Genetics, 2022, v. 18, n. 6, p. 1, doi. 10.1371/journal.pgen.1009798
By:
- Weatherly, Sonia M.;
- Collin, Gayle B.;
- Charette, Jeremy R.;
- Stone, Lisa;
- Damkham, Nattaya;
- Hyde, Lillian F.;
- Peterson, James G.;
- Hicks, Wanda;
- Carter, Gregory W.;
- Naggert, Jürgen K.;
- Krebs, Mark P.;
- Nishina, Patsy M.
Publication type:
Article

Found: 4

A Dpagt1 Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice.

A Splicing Mutation in Slc4a5 Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction.

Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1<sup>rd8</sup> mouse model.