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Large proportion of low frequency microsatellite-instability and loss of heterozygosity in pheochromocytoma and endocrine tumors detected with an extended marker panel.
Published in:
Journal of Cancer Research & Clinical Oncology, 2008, v. 134, n. 4, p. 463, doi. 10.1007/s00432-007-0307-9
By:
- Kupka, Susan;
- Haack, Birgit;
- Zdichavsky, Marty;
- Mlinar, Tanja;
- Kienzle, Christine;
- Bock, Thomas;
- Kandolf, Reinhard;
- Kroeber, Stefan-Martin;
- Königsrainer, Alfred
Publication type:
Article
PGK1 a Potential Marker for Peritoneal Dissemination in Gastric Cancer.
Published in:
Cellular Physiology & Biochemistry (Karger AG), 2008, v. 21, n. 5/6, p. 429, doi. 10.1159/000129635
By:
- Zieker, Derek;
- Königsrainer, Ingmar;
- Traub, Frank;
- Nieselt, Kay;
- Knapp, Bettina;
- Schillinger, Christian;
- Stirnkorb, Christian;
- Fend, Falko;
- Northoff, Hinnak;
- Kupka, Susan;
- Brücher, Björn L. D. M.;
- Königsrainer, Alfred
Publication type:
Article
A Genotype-Phenotype Correlation with Gender-Effect for Hearing Impairment Caused by TECTA Mutations.
Published in:
Cellular Physiology & Biochemistry (Karger AG), 2004, v. 14, n. 4-6, p. 369, doi. 10.1159/000080347
By:
- Pfister, Markus;
- Thiele, Holger;
- Van Camp, Guy;
- Fransen, Erik;
- Apaydin, Fazil;
- Aydin, Ömer;
- Leistenschneider, Peter;
- Devoto, Marcella;
- Zenner, Hans-Peter;
- Blin, Nikolaus;
- Nürnberg, Peter;
- Ozkarakas, Haluk;
- Kupka, Susan
Publication type:
Article
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.
Published in:
Human Genetics, 2002, v. 110, n. 5, p. 389, doi. 10.1007/s00439-002-0719-1
By:
- Cryns, Kim;
- Pfister, Markus;
- Pennings, Ronald J. E.;
- Bom, Steven J. H.;
- Flothmann, Kris;
- Caethoven, Goele;
- Kremer, Hannie;
- Schatteman, Isabelle;
- Köln, Karen A.;
- Tóth, Tímea;
- Kupka, Susan;
- Blin, Nikolaus;
- Nürnberg, Peter;
- Thiele, Holger;
- van de Heyning, Paul H.;
- Reardon, William;
- Stephens, Dafydd;
- Cremers, Cor W. R. J.;
- Smith, Richard J. H.;
- Camp, Guy Van
Publication type:
Article
MSH2 and CXCR4 involvement in malignant VIPoma.
Published in:
World Journal of Surgical Oncology, 2012, v. 10, n. 1, p. 264, doi. 10.1186/1477-7819-10-264
By:
- Mller, Sven;
- Kupka, Susan;
- K”nigsrainer, Ingmar;
- Northoff, Hinnak;
- Sotlar, Karl;
- Bock, Thomas;
- Kandolf, Reinhard;
- Traub, Frank;
- K”nigsrainer, Alfred;
- Zieker, Derek
Publication type:
Article
Cancer immunoediting by GITR (glucocorticoid-induced TNF-related protein) ligand in humans: NK cell/tumor cell interactions.
Published in:
FASEB Journal, 2007, v. 21, n. 10, p. 2442, doi. 10.1096/fj.06-7724com
By:
- Baltz, Katrin M.;
- Krusch, Matthias;
- Bringmann, Anita;
- Brossart, Peter;
- Mayer, Frank;
- Kloss, Mercedes;
- Baessler, Tina;
- Kumbier, Ingrid;
- Peterfi, Andrea;
- Kupka, Susan;
- Kroeber, Stefan;
- Menzel, Dagmar;
- Radsak, Markus P.;
- Rammensee, Hans-Georg;
- Salih, Helmut R.
Publication type:
Article
High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients.
Published in:
Human Mutation, 2005, v. 25, n. 6, p. 595, doi. 10.1002/humu.9345
By:
- Schulte, Claudia;
- Geisthoff, Urban;
- Lux, Andreas;
- Kupka, Susan;
- Zenner, Hans-Peter;
- Blin, Nikolaus;
- Pfister, Markus
Publication type:
Article
GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary.
Published in:
Human Mutation, 2004, v. 23, n. 6, p. 631, doi. 10.1002/humu.9250
By:
- Tóth, Tímea;
- Kupka, Susan;
- Haack, Birgit;
- Riemann, Kathrin;
- Braun, Simone;
- Fazakas, Ferenc;
- Zenner, Hans-Peter;
- Muszbek, László;
- Blin, Nikolaus;
- Pfister, Markus;
- Sziklai, István
Publication type:
Article
Frequencies of GJB2 mutations in German control individuals and patients showing sporadic non-syndromic hearing impairment.
Published in:
Human Mutation, 2002, v. 20, n. 1, p. 77, doi. 10.1002/humu.9044
By:
- Kupka, Susan;
- Braun, Simone;
- Aberle, Susanne;
- Haack, Birgit;
- Ebauer, Margret;
- Zeißler, Ulrike;
- Zenner, Hans-Peter;
- Blin, Nikolaus;
- Pfister, Markus
Publication type:
Article
Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
Published in:
Human Mutation, 2002, v. 19, n. 3, p. 308, doi. 10.1002/humu.9017
By:
- Kupka, Susan;
- Tóth, Tímea;
- Wróbel, Maciej;
- Zeißler, Ulrike;
- Szyfter, Witold;
- Szyfter, Krzysztof;
- Niedzielska, Grazyna;
- Bal, Jerzy;
- Zenner, Hans-Peter;
- Sziklai, István;
- Blin, Nikolaus;
- Pfister, Markus
Publication type:
Article
Genotype-phenotype correlation in a new family with TECTA mutation
Published in:
2003
By:
- Pfister, Markus H.F.;
- Ozkarakas, Haluk;
- Van Camp, Guy;
- Blin, Nikolaus;
- Zenner, Hans Peter;
- Nuernberg, Peter;
- Kupka, Susan
Publication type:
Abstract

Found: 11