Hoffjan S - Search Results

1

Association of interleukin-8 receptor alpha polymorphisms with chronic obstructive pulmonary disease and asthma.

Stemmler S, Arinir U, Klein W, Rohde G, Hoffjan S, Wirkus N, Reinitz-Rademacher K, Bufe A, Schultze-Werninghaus G, Epplen JT. Stemmler S, et al. Among authors: hoffjan s. Genes Immun. 2005 May;6(3):225-30. doi: 10.1038/sj.gene.6364181. Genes Immun. 2005. PMID: 15772681

2

The genetics of atopic dermatitis: recent findings and future options.

Hoffjan S, Epplen JT. Hoffjan S, et al. J Mol Med (Berl). 2005 Sep;83(9):682-92. doi: 10.1007/s00109-005-0672-2. Epub 2005 May 18. J Mol Med (Berl). 2005. PMID: 15902388 Review.

3

Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease.

Hoffjan S, Stemmler S, Parwez Q, Petrasch-Parwez E, Arinir U, Rohde G, Reinitz-Rademacher K, Schultze-Werninghaus G, Bufe A, Epplen JT. Hoffjan S, et al. BMC Med Genet. 2005 Sep 28;6:34. doi: 10.1186/1471-2350-6-34. BMC Med Genet. 2005. PMID: 16188043 Free PMC article.

4

Asthma genetics 2006: the long and winding road to gene discovery.

Ober C, Hoffjan S. Ober C, et al. Among authors: hoffjan s. Genes Immun. 2006 Mar;7(2):95-100. doi: 10.1038/sj.gene.6364284. Genes Immun. 2006. PMID: 16395390 Review.

5

Electrophoresis of DNA in human genetic diagnostics - state-of-the-art, alternatives and future prospects.

Gödde R, Akkad DA, Arning L, Dekomien G, Herchenbach J, Kunstmann E, Meins M, Wieczorek S, Epplen JT, Hoffjan S. Gödde R, et al. Among authors: hoffjan s. Electrophoresis. 2006 Mar;27(5-6):939-46. doi: 10.1002/elps.200500675. Electrophoresis. 2006. PMID: 16470775 Review.

6

Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1.

Hoffjan S, Thiels C, Vorgerd M, Neuen-Jacob E, Epplen JT, Kress W. Hoffjan S, et al. Neuromuscul Disord. 2006 Nov;16(11):749-53. doi: 10.1016/j.nmd.2006.07.020. Epub 2006 Sep 26. Neuromuscul Disord. 2006. PMID: 17005396

7

Two common loss-of-function mutations within the filaggrin gene predispose for early onset of atopic dermatitis.

Stemmler S, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S. Stemmler S, et al. Among authors: hoffjan s. J Invest Dermatol. 2007 Mar;127(3):722-4. doi: 10.1038/sj.jid.5700579. Epub 2006 Sep 28. J Invest Dermatol. 2007. PMID: 17008875 Free article. No abstract available.

8

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

9

Association of toll-interacting protein gene polymorphisms with atopic dermatitis.

Schimming TT, Parwez Q, Petrasch-Parwez E, Nothnagel M, Epplen JT, Hoffjan S. Schimming TT, et al. Among authors: hoffjan s. BMC Dermatol. 2007 Mar 16;7:3. doi: 10.1186/1471-5945-7-3. BMC Dermatol. 2007. PMID: 17362526 Free PMC article.

10

On the role of the epidermal differentiation complex in ichthyosis vulgaris, atopic dermatitis and psoriasis.

Hoffjan S, Stemmler S. Hoffjan S, et al. Br J Dermatol. 2007 Sep;157(3):441-9. doi: 10.1111/j.1365-2133.2007.07999.x. Epub 2007 Jun 15. Br J Dermatol. 2007. PMID: 17573887 Review.

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