ZFIN Lab: Jobst-Schwan Lab

ZFIN ID: ZDB-LAB-200129-2

Jobst-Schwan Lab

PI/Director:	Jobst-Schwan, Tilman
Contact Person:	Jobst-Schwan, Tilman
Email:	Tilman.jobst@uk-erlangen.de
URL:
Address:	Dept. Nephrology and Hypertension University Erlangen-Nuremberg Ulmenweg 18 91054 Erlangen
Country:	Germany
Phone:	+49 9131 85 39564
Fax:	+49 9131 85 39561
Line Designation:	en

GENOMIC FEATURES ORIGINATING FROM THIS LAB No data available

STATEMENT OF RESEARCH INTERESTS

LAB MEMBERS

Haak, Jan René Graduate Student	Pollinger, Lena Graduate Student	Kolb, Cathiana Research Staff
Roessler, Susanne Technical Staff

ZEBRAFISH PUBLICATIONS OF LAB MEMBERS

Cazorla-Vázquez, S., Kösters, P., Bertz, S., Pfister, F., Daniel, C., Dedden, M., Zundler, S., Jobst-Schwan, T., Amann, K., Engel, F.B. (2023) Adhesion GPCR Gpr126 (Adgrg6) Expression Profiling in Zebrafish, Mouse, and Human Kidney. Cells. 12(15):

Tossidou, I., Teng, B., Worthmann, K., Müller-Deile, J., Jobst-Schwan, T., Kardinal, C., Schroder, P., Bolanos-Palmieri, P., Haller, H., Willerding, J., Drost, D.M., de Jonge, L., Reubold, T., Eschenburg, S., Johnson, R.I., Schiffer, M. (2019) Tyrosine Phosphorylation of CD2AP Affects Stability of the Slit Diaphragm Complex. Journal of the American Society of Nephrology : JASN. 30(7):1220-1237

Jobst-Schwan, T., Hoogstraten, C.A., Kolvenbach, C.M., Schmidt, J.M., Kolb, A., Eddy, K., Schneider, R., Ashraf, S., Widmeier, E., Majmundar, A.J., Hildebrandt, F. (2019) Corticosteroid treatment exacerbates nephrotic syndrome in a zebrafish model of magi2a knockout. Kidney International. 95:1079-1090

Braun, D.A., Lovric, S., Schapiro, D., Schneider, R., Marquez, J., Asif, M., Hussain, M.S., Daga, A., Widmeier, E., Rao, J., Ashraf, S., Tan, W., Lusk, C.P., Kolb, A., Jobst-Schwan, T., Schmidt, J.M., Hoogstraten, C.A., Eddy, K., Kitzler, T.M., Shril, S., Moawia, A., Schrage, K., Khayyat, A.I.A., Lawson, J.A., Gee, H.Y., Warejko, J.K., Hermle, T., Majmundar, A.J., Hugo, H., Budde, B., Motameny, S., Altmüller, J., Noegel, A.A., Fathy, H.M., Gale, D.P., Waseem, S.S., Khan, A., Kerecuk, L., Hashmi, S., Mohebbi, N., Ettenger, R., Serdaroğlu, E., Alhasan, K.A., Hashem, M., Goncalves, S., Ariceta, G., Ubetagoyena, M., Antonin, W., Baig, S.M., Alkuraya, F.S., Shen, Q., Xu, H., Antignac, C., Lifton, R.P., Mane, S., Nürnberg, P., Khokha, M.K., Hildebrandt, F. (2018) Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome. The Journal of Clinical Investigation. 128(10):4313-4328

Jobst-Schwan, T., Schmidt, J.M., Schneider, R., Hoogstraten, C.A., Ullmann, J.F.P., Schapiro, D., Majmundar, A.J., Kolb, A., Eddy, K., Shril, S., Braun, D.A., Poduri, A., Hildebrandt, F. (2018) Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish model. PLoS One. 13:e0191503

Braun, D.A., Rao, J., Mollet, G., Schapiro, D., Daugeron, M.C., Tan, W., Gribouval, O., Boyer, O., Revy, P., Jobst-Schwan, T., Schmidt, J.M., Lawson, J.A., Schanze, D., Ashraf, S., Ullmann, J.F.P., Hoogstraten, C.A., Boddaert, N., Collinet, B., Martin, G., Liger, D., Lovric, S., Furlano, M., Guerrera, I.C., Sanchez-Ferras, O., Hu, J.F., Boschat, A.C., Sanquer, S., Menten, B., Vergult, S., De Rocker, N., Airik, M., Hermle, T., Shril, S., Widmeier, E., Gee, H.Y., Choi, W.I., Sadowski, C.E., Pabst, W.L., Warejko, J.K., Daga, A., Basta, T., Matejas, V., Scharmann, K., Kienast, S.D., Behnam, B., Beeson, B., Begtrup, A., Bruce, M., Ch'ng, G.S., Lin, S.P., Chang, J.H., Chen, C.H., Cho, M.T., Gaffney, P.M., Gipson, P.E., Hsu, C.H., Kari, J.A., Ke, Y.Y., Kiraly-Borri, C., Lai, W.M., Lemyre, E., Littlejohn, R.O., Masri, A., Moghtaderi, M., Nakamura, K., Ozaltin, F., Praet, M., Prasad, C., Prytula, A., Roeder, E.R., Rump, P., Schnur, R.E., Shiihara, T., Sinha, M.D., Soliman, N.A., Soulami, K., Sweetser, D.A., Tsai, W.H., Tsai, J.D., Topaloglu, R., Vester, U., Viskochil, D.H., Vatanavicharn, N., Waxler, J.L., Wierenga, K.J., Wolf, M.T.F., Wong, S.N., Leidel, S.A., Truglio, G., Dedon, P.C., Poduri, A., Mane, S., Lifton, R.P., Bouchard, M., Kannu, P., Chitayat, D., Magen, D., Callewaert, B., van Tilbeurgh, H., Zenker, M., Antignac, C., Hildebrandt, F. (2017) Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nature Genetics. 49(10):1529-1538