Samardzija M - Search Results

1

OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and Dent disease.

Festa BP, Berquez M, Gassama A, Amrein I, Ismail HM, Samardzija M, Staiano L, Luciani A, Grimm C, Nussbaum RL, De Matteis MA, Dorchies OM, Scapozza L, Wolfer DP, Devuyst O. Festa BP, et al. Among authors: samardzija m. Hum Mol Genet. 2019 Jun 15;28(12):1931-1946. doi: 10.1093/hmg/ddy449. Hum Mol Genet. 2019. PMID: 30590522 Free PMC article.

2

HIF-1-induced erythropoietin in the hypoxic retina protects against light-induced retinal degeneration.

Grimm C, Wenzel A, Groszer M, Mayser H, Seeliger M, Samardzija M, Bauer C, Gassmann M, Remé CE. Grimm C, et al. Among authors: samardzija m. Nat Med. 2002 Jul;8(7):718-24. doi: 10.1038/nm723. Epub 2002 Jun 17. Nat Med. 2002. PMID: 12068288

3

The genetic modifier Rpe65Leu(450): effect on light damage susceptibility in c-Fos-deficient mice.

Wenzel A, Grimm C, Samardzija M, Remé CE. Wenzel A, et al. Among authors: samardzija m. Invest Ophthalmol Vis Sci. 2003 Jun;44(6):2798-802. doi: 10.1167/iovs.02-1134. Invest Ophthalmol Vis Sci. 2003. PMID: 12766089

4

Constitutive overexpression of human erythropoietin protects the mouse retina against induced but not inherited retinal degeneration.

Grimm C, Wenzel A, Stanescu D, Samardzija M, Hotop S, Groszer M, Naash M, Gassmann M, Remé C. Grimm C, et al. Among authors: samardzija m. J Neurosci. 2004 Jun 23;24(25):5651-8. doi: 10.1523/JNEUROSCI.1288-04.2004. J Neurosci. 2004. PMID: 15215287 Free PMC article.

5

Molecular mechanisms of light-induced photoreceptor apoptosis and neuroprotection for retinal degeneration.

Wenzel A, Grimm C, Samardzija M, Remé CE. Wenzel A, et al. Among authors: samardzija m. Prog Retin Eye Res. 2005 Mar;24(2):275-306. doi: 10.1016/j.preteyeres.2004.08.002. Epub 2004 Nov 11. Prog Retin Eye Res. 2005. PMID: 15610977 Review.

6

Rpe65 as a modifier gene for inherited retinal degeneration.

Samardzija M, Wenzel A, Naash M, Remé CE, Grimm C. Samardzija M, et al. Eur J Neurosci. 2006 Feb;23(4):1028-34. doi: 10.1111/j.1460-9568.2006.04639.x. Eur J Neurosci. 2006. PMID: 16519667 Free PMC article.

7

The prion protein is neuroprotective against retinal degeneration in vivo.

Frigg R, Wenzel A, Samardzija M, Oesch B, Wariwoda H, Navarini AA, Seeliger MW, Tanimoto N, Remé C, Grimm C. Frigg R, et al. Among authors: samardzija m. Exp Eye Res. 2006 Dec;83(6):1350-8. doi: 10.1016/j.exer.2006.07.010. Epub 2006 Sep 6. Exp Eye Res. 2006. PMID: 16952355

8

Differential role of Jak-STAT signaling in retinal degenerations.

Samardzija M, Wenzel A, Aufenberg S, Thiersch M, Remé C, Grimm C. Samardzija M, et al. FASEB J. 2006 Nov;20(13):2411-3. doi: 10.1096/fj.06-5895fje. Epub 2006 Sep 11. FASEB J. 2006. PMID: 16966486

9

Caspase-1 ablation protects photoreceptors in a model of autosomal dominant retinitis pigmentosa.

Samardzija M, Wenzel A, Thiersch M, Frigg R, Remé C, Grimm C. Samardzija M, et al. Invest Ophthalmol Vis Sci. 2006 Dec;47(12):5181-90. doi: 10.1167/iovs.06-0556. Invest Ophthalmol Vis Sci. 2006. PMID: 17122101

10

R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal.

Samardzija M, von Lintig J, Tanimoto N, Oberhauser V, Thiersch M, Remé CE, Seeliger M, Grimm C, Wenzel A. Samardzija M, et al. Hum Mol Genet. 2008 Jan 15;17(2):281-92. doi: 10.1093/hmg/ddm304. Epub 2007 Oct 12. Hum Mol Genet. 2008. PMID: 17933883 Free article.

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