Handschug K - Search Results

1

New insights into the molecular basis of the triple A syndrome.

Huebner A, Kaindl AM, Braun R, Handschug K. Huebner A, et al. Among authors: handschug k. Endocr Res. 2002 Nov;28(4):733-9. doi: 10.1081/erc-120016998. Endocr Res. 2002. PMID: 12530689

2

Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene.

Handschug K, Sperling S, Yoon SJ, Hennig S, Clark AJ, Huebner A. Handschug K, et al. Hum Mol Genet. 2001 Feb 1;10(3):283-90. doi: 10.1093/hmg/10.3.283. Hum Mol Genet. 2001. PMID: 11159947

3

Triple A syndrome--clinical aspects and molecular genetics.

Huebner A, Yoon SJ, Ozkinay F, Hilscher C, Lee H, Clark AJ, Handschug K. Huebner A, et al. Among authors: handschug k. Endocr Res. 2000 Nov;26(4):751-9. doi: 10.3109/07435800009048596. Endocr Res. 2000. PMID: 11196451

4

Chromosomal fragility in patients with triple A syndrome.

Reshmi-Skarja S, Huebner A, Handschug K, Finegold DN, Clark AJ, Gollin SM. Reshmi-Skarja S, et al. Among authors: handschug k. Am J Med Genet A. 2003 Feb 15;117A(1):30-6. doi: 10.1002/ajmg.a.10846. Am J Med Genet A. 2003. PMID: 12548737

5

Triple A syndrome: genotype-phenotype assessment.

Prpic I, Huebner A, Persic M, Handschug K, Pavletic M. Prpic I, et al. Among authors: handschug k. Clin Genet. 2003 May;63(5):415-7. doi: 10.1034/j.1399-0004.2003.00070.x. Clin Genet. 2003. PMID: 12752575

6

The importance of the alpha 2MR/LRP for human genetics. Investigations of the receptor expression in different human blood cells.

Gläser C, Handschug K, Ludvik S, Schell U, Hehr A, Küchenhoff A, Robenek H. Gläser C, et al. Among authors: handschug k. Ann N Y Acad Sci. 1994 Sep 10;737:447-50. doi: 10.1111/j.1749-6632.1994.tb44336.x. Ann N Y Acad Sci. 1994. PMID: 7944149 No abstract available.

7

Low-density lipoprotein receptor-related protein in atherosclerosis development: up-regulation of gene expression in patients with coronary obstruction.

Handschug K, Schulz S, Schnürer C, Köhler S, Wenzel K, Teichmann W, Gläser C. Handschug K, et al. J Mol Med (Berl). 1998 Jul;76(8):596-600. doi: 10.1007/s001090050255. J Mol Med (Berl). 1998. PMID: 9694437

8

Genetic and functional characteristics of the human in vivo LRP1/A2MR receptor suggested as a risk marker for Alzheimer's disease and other complex (degenerative) diseases.

Gläser C, Schulz S, Handschug K, Huse K, Birkenmeier G. Gläser C, et al. Among authors: handschug k. Neurosci Res. 2004 Sep;50(1):85-101. doi: 10.1016/j.neures.2004.06.001. Neurosci Res. 2004. PMID: 15288502

9

Different expression of the alpha2-macroglobulin receptor/low-density lipoprotein receptor-related protein in human keratinocytes and fibroblasts.

Birkenmeier G, Heidrich K, Gläser C, Handschug K, Fabricius EM, Frank R, Reissig D. Birkenmeier G, et al. Among authors: handschug k. Arch Dermatol Res. 1998 Oct;290(10):561-8. doi: 10.1007/s004030050352. Arch Dermatol Res. 1998. PMID: 9836507

10

Angiotensin-converting enzyme gene insertion/deletion polymorphism and peripheral arterial occlusive disease.

Taute BM, Handschug K, Taute R, Seifert H, Gläser C, Podhaisky H. Taute BM, et al. Among authors: handschug k. Vasa. 1998 Aug;27(3):149-53. Vasa. 1998. PMID: 9747149

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