Petrasch-Parwez E - Search Results

1

SOX9 duplication linked to intersex in deer.

Kropatsch R, Dekomien G, Akkad DA, Gerding WM, Petrasch-Parwez E, Young ND, Altmüller J, Nürnberg P, Gasser RB, Epplen JT. Kropatsch R, et al. PLoS One. 2013 Sep 6;8(9):e73734. doi: 10.1371/journal.pone.0073734. eCollection 2013. PLoS One. 2013. PMID: 24040047 Free PMC article.

2

Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients.

Akkad DA, Hoffjan S, Petrasch-Parwez E, Beygo J, Gold R, Epplen JT. Akkad DA, et al. J Autoimmun. 2009 Mar;32(2):110-5. doi: 10.1016/j.jaut.2009.01.002. Epub 2009 Feb 23. J Autoimmun. 2009. PMID: 19231135

3

Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.

Dekomien G, Vollrath C, Petrasch-Parwez E, Boevé MH, Akkad DA, Gerding WM, Epplen JT. Dekomien G, et al. Neurogenetics. 2010 May;11(2):163-74. doi: 10.1007/s10048-009-0223-z. Epub 2009 Sep 24. Neurogenetics. 2010. PMID: 19777273

4

Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene.

Kropatsch R, Petrasch-Parwez E, Seelow D, Schlichting A, Gerding WM, Akkad DA, Epplen JT, Dekomien G. Kropatsch R, et al. Mol Cell Probes. 2010 Dec;24(6):357-63. doi: 10.1016/j.mcp.2010.07.007. Epub 2010 Aug 4. Mol Cell Probes. 2010. PMID: 20691256

5

Ccdc66 null mutation causes retinal degeneration and dysfunction.

Gerding WM, Schreiber S, Schulte-Middelmann T, de Castro Marques A, Atorf J, Akkad DA, Dekomien G, Kremers J, Dermietzel R, Gal A, Rülicke T, Ibrahim S, Epplen JT, Petrasch-Parwez E. Gerding WM, et al. Hum Mol Genet. 2011 Sep 15;20(18):3620-31. doi: 10.1093/hmg/ddr282. Epub 2011 Jun 16. Hum Mol Genet. 2011. PMID: 21680557

6

Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families.

Kastner S, Thiemann IJ, Dekomien G, Petrasch-Parwez E, Schreiber S, Akkad DA, Gerding WM, Hoffjan S, Günes S, Günes S, Bagci H, Epplen JT. Kastner S, et al. Among authors: petrasch parwez e. Invest Ophthalmol Vis Sci. 2015 Dec;56(13):8045-53. doi: 10.1167/iovs.15-17473. Invest Ophthalmol Vis Sci. 2015. PMID: 26720455

7

Haplotype-defined linkage region for gPRA in Schapendoes dogs.

Lippmann T, Jonkisz A, Dobosz T, Petrasch-Parwez E, Epplen JT, Dekomien G. Lippmann T, et al. Mol Vis. 2007 Feb 7;13:174-80. Mol Vis. 2007. PMID: 17327822 Free PMC article.

8

Neurodegeneration in the olfactory bulb and olfactory deficits in the Ccdc66 -/- mouse model for retinal degeneration.

Schreiber S, Petrasch-Parwez E, Porrmann-Kelterbaum E, Förster E, Epplen JT, Gerding WM. Schreiber S, et al. Among authors: petrasch parwez e. IBRO Rep. 2018 Aug 24;5:43-53. doi: 10.1016/j.ibror.2018.08.004. eCollection 2018 Dec. IBRO Rep. 2018. PMID: 30211337 Free PMC article.

9

No evidence of an association between polymorphisms in the IRAK-M gene and atopic dermatitis in a German cohort.

Beygo J, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S. Beygo J, et al. Mol Cell Probes. 2009 Feb;23(1):16-9. doi: 10.1016/j.mcp.2008.10.002. Epub 2008 Oct 26. Mol Cell Probes. 2009. PMID: 19013233

10

Association screen for atopic dermatitis candidate gene regions using microsatellite markers in pooled DNA samples.

Hoffjan S, Parwez Q, Petrasch-Parwez E, Falkenstein D, Nothnagel M, Epplen JT. Hoffjan S, et al. Int J Immunogenet. 2006 Dec;33(6):401-9. doi: 10.1111/j.1744-313X.2006.00631.x. Int J Immunogenet. 2006. PMID: 17117949

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