115 related articles for article (PubMed ID: 29969487)
1. Retinal degeneration mutation in Sftpa1tm1Kor/J and Sftpd -/- targeted mice.
Bhatti F; Kung JW; Vieira F
PLoS One; 2018; 13(7):e0199824. PubMed ID: 29969487
[TBL] [Abstract][Full Text] [Related]
2. Presence of rd8 mutation does not alter the ocular phenotype of late-onset retinal degeneration mouse model.
Sahu B; Chavali VR; Alapati A; Suk J; Bartsch DU; Jablonski MM; Ayyagari R
Mol Vis; 2015; 21():273-84. PubMed ID: 25814825
[TBL] [Abstract][Full Text] [Related]
3. Monitoring mouse retinal degeneration with high-resolution spectral-domain optical coherence tomography.
Kim KH; Puoris'haag M; Maguluri GN; Umino Y; Cusato K; Barlow RB; de Boer JF
J Vis; 2008 Jan; 8(1):17.1-11. PubMed ID: 18318620
[TBL] [Abstract][Full Text] [Related]
4. Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.
Chang B; Hawes NL; Pardue MT; German AM; Hurd RE; Davisson MT; Nusinowitz S; Rengarajan K; Boyd AP; Sidney SS; Phillips MJ; Stewart RE; Chaudhury R; Nickerson JM; Heckenlively JR; Boatright JH
Vision Res; 2007 Mar; 47(5):624-33. PubMed ID: 17267005
[TBL] [Abstract][Full Text] [Related]
5. Influence of genetic variability at the surfactant proteins A and D in community-acquired pneumonia: a prospective, observational, genetic study.
García-Laorden MI; Rodríguez de Castro F; Solé-Violán J; Rajas O; Blanquer J; Borderías L; Aspa J; Briones ML; Saavedra P; Marcos-Ramos JA; González-Quevedo N; Sologuren I; Herrera-Ramos E; Ferrer JM; Rello J; Rodríguez-Gallego C
Crit Care; 2011; 15(1):R57. PubMed ID: 21310059
[TBL] [Abstract][Full Text] [Related]
6. Retinal Macrophages Synthesize C3 and Activate Complement in AMD and in Models of Focal Retinal Degeneration.
Natoli R; Fernando N; Jiao H; Racic T; Madigan M; Barnett NL; Chu-Tan JA; Valter K; Provis J; Rutar M
Invest Ophthalmol Vis Sci; 2017 Jun; 58(7):2977-2990. PubMed ID: 28605809
[TBL] [Abstract][Full Text] [Related]
7. The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation.
Pak JS; Lee EJ; Craft CM
Mol Vis; 2015; 21():1281-94. PubMed ID: 26664249
[TBL] [Abstract][Full Text] [Related]
8. Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.
Chang B; Mandal MN; Chavali VR; Hawes NL; Khan NW; Hurd RE; Smith RS; Davisson ML; Kopplin L; Klein BE; Klein R; Iyengar SK; Heckenlively JR; Ayyagari R
Hum Mol Genet; 2008 Dec; 17(24):3929-41. PubMed ID: 18805803
[TBL] [Abstract][Full Text] [Related]
9. Suppression of developmental retinal cell death but not of photoreceptor degeneration in Bax-deficient mice.
Mosinger Ogilvie J; Deckwerth TL; Knudson CM; Korsmeyer SJ
Invest Ophthalmol Vis Sci; 1998 Aug; 39(9):1713-20. PubMed ID: 9699561
[TBL] [Abstract][Full Text] [Related]
10. Increased susceptibility to fundus camera-delivered light-induced retinal degeneration in mice deficient in oxidative stress response proteins.
Ding Y; Aredo B; Zhong X; Zhao CX; Ufret-Vincenty RL
Exp Eye Res; 2017 Jun; 159():58-68. PubMed ID: 28336262
[TBL] [Abstract][Full Text] [Related]
11. Genetic Association of Pulmonary Surfactant Protein Genes, SFTPA1, SFTPA2, SFTPB, SFTPC, and SFTPD With Cystic Fibrosis.
Lin Z; Thorenoor N; Wu R; DiAngelo SL; Ye M; Thomas NJ; Liao X; Lin TR; Warren S; Floros J
Front Immunol; 2018; 9():2256. PubMed ID: 30333828
[TBL] [Abstract][Full Text] [Related]
12. Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Pang JJ; Chang B; Hawes NL; Hurd RE; Davisson MT; Li J; Noorwez SM; Malhotra R; McDowell JH; Kaushal S; Hauswirth WW; Nusinowitz S; Thompson DA; Heckenlively JR
Mol Vis; 2005 Feb; 11():152-62. PubMed ID: 15765048
[TBL] [Abstract][Full Text] [Related]
13. Development and degeneration of retina in rds mutant mice: light microscopy.
Sanyal S; De Ruiter A; Hawkins RK
J Comp Neurol; 1980 Nov; 194(1):193-207. PubMed ID: 7440795
[TBL] [Abstract][Full Text] [Related]
14. New Developments in Murine Imaging for Assessing Photoreceptor Degeneration In Vivo.
Burns ME; Levine ES; Miller EB; Zam A; Zhang P; Zawadzki RJ; Pugh EN
Adv Exp Med Biol; 2016; 854():269-75. PubMed ID: 26427421
[TBL] [Abstract][Full Text] [Related]
15. Vision deficits precede structural losses in a mouse model of mitochondrial dysfunction and progressive retinal degeneration.
Laliberté AM; MacPherson TC; Micks T; Yan A; Hill KA
Exp Eye Res; 2011 Dec; 93(6):833-41. PubMed ID: 21983042
[TBL] [Abstract][Full Text] [Related]
16. Reduced photoreceptor death and improved retinal function during retinal degeneration in mice lacking innate immunity adaptor protein MyD88.
Syeda S; Patel AK; Lee T; Hackam AS
Exp Neurol; 2015 May; 267():1-12. PubMed ID: 25725353
[TBL] [Abstract][Full Text] [Related]
17. Fertility defects in Surfactant associated protein D knockout female mice: altered ovarian hormone profile.
Kay S; Madan T
Mol Immunol; 2016 Mar; 71():87-97. PubMed ID: 26874827
[TBL] [Abstract][Full Text] [Related]
18. Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function.
Ishiba Y; Higashide T; Mori N; Kobayashi A; Kubota S; McLaren MJ; Satoh H; Wong F; Inana G
Exp Eye Res; 2007 Mar; 84(3):473-85. PubMed ID: 17174953
[TBL] [Abstract][Full Text] [Related]
19. Disruption of the polyubiquitin gene Ubb causes retinal degeneration in mice.
Lim D; Park CW; Ryu KY; Chung H
Biochem Biophys Res Commun; 2019 May; 513(1):35-40. PubMed ID: 30935687
[TBL] [Abstract][Full Text] [Related]
20. Differences in the distribution, phenotype and gene expression of subretinal microglia/macrophages in C57BL/6N (Crb1 rd8/rd8) versus C57BL6/J (Crb1 wt/wt) mice.
Aredo B; Zhang K; Chen X; Wang CX; Li T; Ufret-Vincenty RL
J Neuroinflammation; 2015 Jan; 12():6. PubMed ID: 25588310
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]