Kupka S - Search Results

1

Cancer immunoediting by GITR (glucocorticoid-induced TNF-related protein) ligand in humans: NK cell/tumor cell interactions.

Baltz KM, Krusch M, Bringmann A, Brossart P, Mayer F, Kloss M, Baessler T, Kumbier I, Peterfi A, Kupka S, Kroeber S, Menzel D, Radsak MP, Rammensee HG, Salih HR. Baltz KM, et al. Among authors: kupka s. FASEB J. 2007 Aug;21(10):2442-54. doi: 10.1096/fj.06-7724com. Epub 2007 Mar 14. FASEB J. 2007. PMID: 17360848

2

Deficient membrane integration of the novel p.N14D-GJB2 mutant associated with non-syndromic hearing impairment.

Haack B, Schmalisch K, Palmada M, Böhmer C, Kohlschmidt N, Keilmann A, Zechner U, Limberger A, Beckert S, Zenner HP, Lang F, Kupka S. Haack B, et al. Among authors: kupka s. Hum Mutat. 2006 Nov;27(11):1158-9. doi: 10.1002/humu.9464. Hum Mutat. 2006. PMID: 17041897

3

PGK1 a potential marker for peritoneal dissemination in gastric cancer.

Zieker D, Königsrainer I, Traub F, Nieselt K, Knapp B, Schillinger C, Stirnkorb C, Fend F, Northoff H, Kupka S, Brücher BL, Königsrainer A. Zieker D, et al. Among authors: kupka s. Cell Physiol Biochem. 2008;21(5-6):429-36. doi: 10.1159/000129635. Epub 2008 Apr 24. Cell Physiol Biochem. 2008. PMID: 18453750 Free article.

4

Gene expression analysis in chronic postradiation proctopathy.

Traub F, Schleicher S, Kirschniak A, Zieker D, Kupka S, Weinmann M, Königsrainer A, Kratt T. Traub F, et al. Among authors: kupka s. Int J Colorectal Dis. 2012 Jul;27(7):879-84. doi: 10.1007/s00384-011-1387-1. Epub 2011 Dec 16. Int J Colorectal Dis. 2012. PMID: 22173715

5

Frequencies of GJB2 mutations in German control individuals and patients showing sporadic non-syndromic hearing impairment.

Kupka S, Braun S, Aberle S, Haack B, Ebauer M, Zeissler U, Zenner HP, Blin N, Pfister M. Kupka S, et al. Hum Mutat. 2002 Jul;20(1):77-8. doi: 10.1002/humu.9044. Hum Mutat. 2002. PMID: 12112666

6

GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary.

Tóth T, Kupka S, Haack B, Riemann K, Braun S, Fazakas F, Zenner HP, Muszbek L, Blin N, Pfister M, Sziklai I. Tóth T, et al. Among authors: kupka s. Hum Mutat. 2004 Jun;23(6):631-2. doi: 10.1002/humu.9250. Hum Mutat. 2004. PMID: 15146474

7

Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.

Kupka S, Tóth T, Wróbel M, Zeissler U, Szyfter W, Szyfter K, Niedzielska G, Bal J, Zenner HP, Sziklai I, Blin N, Pfister M. Kupka S, et al. Hum Mutat. 2002 Mar;19(3):308-9. doi: 10.1002/humu.9017. Hum Mutat. 2002. PMID: 11857751

8

A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10.

Pfister M, Tóth T, Thiele H, Haack B, Blin N, Zenner HP, Sziklai I, Nürnberg P, Kupka S. Pfister M, et al. Among authors: kupka s. Mol Med. 2002 Oct;8(10):607-11. Mol Med. 2002. PMID: 12477971 Free PMC article.

9

High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients.

Schulte C, Geisthoff U, Lux A, Kupka S, Zenner HP, Blin N, Pfister M. Schulte C, et al. Among authors: kupka s. Hum Mutat. 2005 Jun;25(6):595. doi: 10.1002/humu.9345. Hum Mutat. 2005. PMID: 15880681

10

[Mitochondrial A1555G mutation. Molecular genetic diagnosis in sporadic cases of non-syndromic hearing impairment].

Kupka S, Bodden-Kamps B, Baur M, Zenner HP, Pfister M. Kupka S, et al. HNO. 2004 Nov;52(11):968-72. doi: 10.1007/s00106-003-0994-8. HNO. 2004. PMID: 15309320 Clinical Trial. German.

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