Schleithoff L - Search Results

1

GSK-3β controls NF-kappaB activity via IKKγ/NEMO.

Medunjanin S, Schleithoff L, Fiegehenn C, Weinert S, Zuschratter W, Braun-Dullaeus RC. Medunjanin S, et al. Among authors: schleithoff l. Sci Rep. 2016 Dec 8;6:38553. doi: 10.1038/srep38553. Sci Rep. 2016. PMID: 27929056 Free PMC article.

2

Aceruloplasminaemia: a family with a novel mutation and long-term therapy with deferasirox.

Lindner U, Schuppan D, Schleithoff L, Habeck JO, Grodde T, Kirchhof K, Stoelzel U. Lindner U, et al. Among authors: schleithoff l. Horm Metab Res. 2015 Apr;47(4):303-8. doi: 10.1055/s-0034-1383650. Epub 2014 Aug 4. Horm Metab Res. 2015. PMID: 25089372

3

Novel ceruloplasmin mutation causing aceruloplasminemia with hepatic iron overload and diabetes without neurological symptoms.

Rusticeanu M, Zimmer V, Schleithoff L, Wonney K, Viera J, Zimmer A, Hübschen U, Bohle RM, Grünhage F, Lammert F. Rusticeanu M, et al. Among authors: schleithoff l. Clin Genet. 2014 Mar;85(3):300-1. doi: 10.1111/cge.12145. Epub 2013 Apr 5. Clin Genet. 2014. PMID: 23557349 No abstract available.

4

Gene symbol: PRSS1. Disease: Pancreatitis, hereditary. Accession #Hm0542.

Schleithoff L, Seelig HP. Schleithoff L, et al. Hum Genet. 2006 Feb;118(6):779. Hum Genet. 2006. PMID: 17297697 No abstract available.

5

Gene symbol: TNFSF5. Disease: Hyper-IgM syndrome. Accession #Hm0539.

Schleithoff LS, Seelig HP. Schleithoff LS, et al. Hum Genet. 2006 Feb;118(6):778. Hum Genet. 2006. PMID: 17297694 No abstract available.

6

Gene symbol: SERPINC1. Disease: Antithrombin deficiency. Accession #Hd0514.

Schleithoff L, Seelig HP. Schleithoff L, et al. Hum Genet. 2006 Feb;118(6):775. Hum Genet. 2006. PMID: 17297683 No abstract available.

7

Loss of wild-type MEN1 gene expression in multiple endocrine neoplasia type 1-associated parathyroid adenoma.

Ludwig L, Schleithoff L, Kessler H, Wagner PK, Boehm BO, Karges W. Ludwig L, et al. Among authors: schleithoff l. Endocr J. 1999 Aug;46(4):539-44. doi: 10.1507/endocrj.46.539. Endocr J. 1999. PMID: 10580746 Free article.

8

Genomic structure and functional expression of a human alpha(2)/delta calcium channel subunit gene (CACNA2).

Schleithoff L, Mehrke G, Reutlinger B, Lehmann-Horn F. Schleithoff L, et al. Genomics. 1999 Oct 15;61(2):201-9. doi: 10.1006/geno.1999.5941. Genomics. 1999. PMID: 10534405

9

Screening of the ryanodine receptor gene in 105 malignant hyperthermia families: novel mutations and concordance with the in vitro contracture test.

Brandt A, Schleithoff L, Jurkat-Rott K, Klingler W, Baur C, Lehmann-Horn F. Brandt A, et al. Among authors: schleithoff l. Hum Mol Genet. 1999 Oct;8(11):2055-62. doi: 10.1093/hmg/8.11.2055. Hum Mol Genet. 1999. PMID: 10484775

10

A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions.

Lerche H, Biervert C, Alekov AK, Schleithoff L, Lindner M, Klinger W, Bretschneider F, Mitrovic N, Jurkat-Rott K, Bode H, Lehmann-Horn F, Steinlein OK. Lerche H, et al. Among authors: schleithoff l. Ann Neurol. 1999 Sep;46(3):305-12. doi: 10.1002/1531-8249(199909)46:3<305::aid-ana5>3.0.co;2-5. Ann Neurol. 1999. PMID: 10482260

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