Publications (selected)

2018

Wunderlich, G., Brunn, A., Daimagüler, H.S., Bozoglu, T., Fink, G.R., Lehmann, H.C., Weis, J. and Cirak, S. Long term history of a congenital core-rod myopathy with compound heterozygous mutations in the Nebulin gene. Acta Myologica, 37(2), p.121.

Dorn, T., Kornherr, J., Parrotta, E. I., Zawada, D., Ayetey, H., Santamaria, G., Iop, L., Mastantuono, E., Sinnecker, D., Goedel, A., Dirschinger, R. J., My, I., Laue, S., Bozoglu, T., Baarlink, C., Ziegler, T., Graf, E., Hinkel, R., Cuda, G., Kääb, S., Grace, A. A., Grosse, R., Kupatt, C., Meitinger, T., Smith, A. G., Laugwitz, K. L., Moretti, A. Interplay of cell-cell contacts and RhoA/MRTF-A signaling regulates cardiomyocyte identity. The EMBO journal, 37(12), e98133.

Bozoglu T, Hinkel R, Kupatt C. Therapeutic Potential of Heme Oxygenase 1 in Ischemia Reperfusion Injury. J Transplant Technol Res. 6(162):2161-0991.

Seven, M., Güven, A., Bozoglu, T. M., & Tolun, A. Detecting PORCN microdeletions in a large family with focal dermal hypoplasia. Genetic Counseling, 26(2), 195.

Spyroglou A, Sabrautzki S, Rathkolb B, Bozoglu T, et al. Gender-, strain-, and inheritance-dependent variation in aldosterone secretion in mice. J Endocrinol. Dec;215(3):375-81.
Bozoglu T, et al. Low SLC26A2 expression in adrenal cells is associated with high aldosterone output. BioScientifica, May;29.
Guven A, Gunduz A, Bozoglu TM, et al. Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly. Neurogenetics. Aug;13(3):18994.

Behunova J; Zavadilikova E; Bozoglu T, et al. Familial microhydranencephaly, a family that does not map to 16p13.13-p12.2: relationship with hereditary fetal brain degeneration and fetal brain disruption sequence. Clin Dysmorph., Jul;19(3):107-18.
Spyroglou A, Wagner S, Bidlingmaier M, Bozoglu M, et al. A mouse model with hyperaldosteronism carrying an ENU induced mutation on chromosome 9. BioScientifica, April;22.