Transcriptional regulation of SLC24A4 (pendrin), a protein causing Pendred-Syndrome, a human hereditary disease associated with deafness and goiter

Projekt: Forschung

PMU-FFF E-09/10/055-PAM

Status	Abgeschlossen
Tatsächlicher Beginn/ -es Ende	19/02/10 → 18/02/12

Functional characterization of pendrin mutations found in the Israeli and Palestinian populations.
Dossena, S. (Erstautor/-in), Nofziger, C. (Co-Autor/-in), Brownstein, Z., Kanaan, M., Avraham, K. B. & Paulmichl, M. (Letztautor/-in), 2011, in: Cellular physiology and biochemistry. 28, 3, S. 477-484
Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung

24 Quellenangaben (Web of Science)
Identification of allelic variants of pendrin (SLC26A4) with loss and gain of function.
Dossena, S. (Erstautor/-in), Bizhanova, A., Nofziger, C. (Co-Autor/-in), Bernardinelli, E., Ramsauer, J., Kopp, P. & Paulmichl, M. (Letztautor/-in), 2011, in: Cellular physiology and biochemistry. 28, 3, S. 4-76
Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung

38 Quellenangaben (Web of Science)
Methylation of the human pendrin promoter.
Lee, A., Nofziger, C. (Co-Autor/-in), Dossena, S. (Co-Autor/-in), Vanoni, S., Diasio, R. & Paulmichl, M. (Letztautor/-in), 2011, in: Cellular physiology and biochemistry. 28, 3, S. 397-406
Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung

7 Quellenangaben (Web of Science)

Projektdetails