Akkad DA - Search Results

1

ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease.

Arning L, Monté D, Hansen W, Wieczorek S, Jagiello P, Akkad DA, Andrich J, Kraus PH, Saft C, Epplen JT. Arning L, et al. Among authors: akkad da. J Mol Med (Berl). 2008 Apr;86(4):485-90. doi: 10.1007/s00109-007-0299-6. Epub 2008 Mar 8. J Mol Med (Berl). 2008. PMID: 18327563

2

PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease.

Taherzadeh-Fard E, Saft C, Akkad DA, Wieczorek S, Haghikia A, Chan A, Epplen JT, Arning L. Taherzadeh-Fard E, et al. Among authors: akkad da. Mol Neurodegener. 2011 May 19;6(1):32. doi: 10.1186/1750-1326-6-32. Mol Neurodegener. 2011. PMID: 21595933 Free PMC article.

3

Association of age at onset in Huntington disease with functional promoter variations in NPY and NPY2R.

Kloster E, Saft C, Akkad DA, Epplen JT, Arning L. Kloster E, et al. Among authors: akkad da. J Mol Med (Berl). 2014 Feb;92(2):177-84. doi: 10.1007/s00109-013-1092-3. J Mol Med (Berl). 2014. PMID: 24121255

4

On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors.

Wagenleiter SE, Jagiello P, Akkad DA, Arning L, Griga T, Klein W, Epplen JT. Wagenleiter SE, et al. Among authors: akkad da. J Negat Results Biomed. 2005 Nov 30;4:8. doi: 10.1186/1477-5751-4-8. J Negat Results Biomed. 2005. PMID: 16318629 Free PMC article.

5

Genomic NGFB variation and multiple sclerosis in a case control study.

Akkad DA, Kruse N, Arning L, Gold R, Epplen JT. Akkad DA, et al. BMC Med Genet. 2008 Dec 8;9:107. doi: 10.1186/1471-2350-9-107. BMC Med Genet. 2008. PMID: 19063739 Free PMC article.

6

Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults.

Ocklenburg S, Arning L, Gerding WM, Hengstler JG, Epplen JT, Güntürkün O, Beste C, Akkad DA. Ocklenburg S, et al. Among authors: akkad da. Mol Neurobiol. 2016 Nov;53(9):6355-6361. doi: 10.1007/s12035-015-9534-2. Epub 2015 Nov 16. Mol Neurobiol. 2016. PMID: 26572639

7

Polymorphisms in genes encoding leptin, ghrelin and their receptors in German multiple sclerosis patients.

Rey LK, Wieczorek S, Akkad DA, Linker RA, Chan A, Hoffjan S. Rey LK, et al. Among authors: akkad da. Mol Cell Probes. 2011 Oct-Dec;25(5-6):255-9. doi: 10.1016/j.mcp.2011.05.004. Epub 2011 Jun 12. Mol Cell Probes. 2011. PMID: 21664965

8

Multiple sclerosis in families: risk factors beyond known genetic polymorphisms.

Akkad DA, Lee DH, Bruch K, Haghikia A, Epplen JT, Hoffjan S, Linker RA. Akkad DA, et al. Neurogenetics. 2016 Apr;17(2):131-5. doi: 10.1007/s10048-016-0474-4. Epub 2016 Feb 11. Neurogenetics. 2016. PMID: 26865406

9

No association between synapsin III gene promoter polymorphisms and multiple sclerosis in German patients.

Akkad DA, Gödde R, Epplen JT. Akkad DA, et al. J Neurol. 2006 Oct;253(10):1365-6. doi: 10.1007/s00415-006-0214-z. Epub 2006 Sep 13. J Neurol. 2006. PMID: 16972123

10

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. Among authors: akkad da. Neurogenetics. 2010 May;11(2):163-74. doi: 10.1007/s10048-009-0223-z. Epub 2009 Sep 24. Neurogenetics. 2010. PMID: 19777273

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