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1دورية أكاديمية
المؤلفون: Grand, K., Stoltz, M., Rizzo, L., Röck, R., Kaminski, M.M., Salinas, G., Getwan, M., Naert, T., Pichler, R., Lienkamp, S.S.
مصطلحات موضوعية: Cardiovascular and Metabolic Diseases, Topic 1: Genes, Cells and Cell-Based Medicine
وصف الملف: application/pdf; other
العلاقة: http://edoc.mdc-berlin.de/22972/1/22972oa.pdfTest; http://edoc.mdc-berlin.de/22972/2/22972suppl.zipTest; HNF1B alters an evolutionarily conserved nephrogenic program of target genes. Grand, K. and Stoltz, M. and Rizzo, L. and Röck, R. and Kaminski, M.M. and Salinas, G. and Getwan, M. and Naert, T. and Pichler, R. and Lienkamp, S.S. Journal of the American Society of Nephrology 34 (3): 412-432. March 2023
الإتاحة: https://doi.org/10.1681/ASN.2022010076Test
http://edoc.mdc-berlin.de/22972Test/
https://edoc.mdc-berlin.de/22972Test/
http://edoc.mdc-berlin.de/22972/1/22972oa.pdfTest
http://edoc.mdc-berlin.de/22972/2/22972suppl.zipTest -
2دورية أكاديميةPOS-430 CRISPR/CAS9 TARGETING TTTC30A MIMICS CILIARY CHONDRODYSPLASIA WITH POLYCYSTIC KIDNEY DISEASE
المؤلفون: Getwan, M., Hoppmann, A., Schlosser, P., Köttgen, A., Kelli, G., LIENKAMP, S.
المصدر: Kidney International Reports ; volume 6, issue 4, page S187 ; ISSN 2468-0249
مصطلحات موضوعية: Nephrology
الإتاحة: https://doi.org/10.1016/j.ekir.2021.03.453Test
https://api.elsevier.com/content/article/PII:S2468024921005994?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2468024921005994?httpAccept=text/plainTest -
3دورية أكاديمية
المؤلفون: Vivante, A, Mann, N, Yonath, H, Weiss, A-C, Getwan, M, Kaminski, MM, Bohnenpoll, T, Teyssier, C, Chen, J, Shril, S, van der Ven, AT, Ityel, H, Schmidt, JM, Widmeier, E, Bauer, SB, Sanna-Cherchi, S, Gharavi, AG, Lu, W, Magen, D, Shukrun, R, Lifton, RP, Tasic, V, Stanescu, HC, Cavaillès, V, Kleta, R, Anikster, Y, Dekel, B, Kispert, A, Lienkamp, SS, Hildebrandt, F
المصدر: Journal of the American Society of Nephrology , 28 (8) pp. 2364-2376. (2017)
مصطلحات موضوعية: CAKUT, NRIP1, retinoic acid
وصف الملف: text
العلاقة: https://discovery.ucl.ac.uk/id/eprint/1551010/1/Kleta_NRIP1_Manuscript_Ver%207-1-RK%20%282%29.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1551010Test/
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4دورية أكاديميةPOS-430 CRISPR/CAS9 TARGETING TTTC30A MIMICS CILIARY CHONDRODYSPLASIA WITH POLYCYSTIC KIDNEY DISEASE
المؤلفون: Kelli, G., Schlosser, P., Getwan, M., Hoppmann, A., Köttgen, A., Lienkamp, S.
المصدر: Kidney International Reports. - 6, 4 (2021) , S187, ISSN: 2468-0249
الإتاحة: https://doi.org/10.1016/j.ekir.2021.03.453Test
https://freidok.uni-freiburg.de/data/248433Test -
5دورية أكاديمية
المؤلفون: Klämbt, V., Werth, M., Onuchic-Whitford, A.C., Getwan, M., Kitzler, T.M., Buerger, F., Mao, Y., Deutsch, K., Mann, N., Majmundar, A.J., Kaminski, M.M., Shen, Tian, Schmidt-Ott, K.M., Shalaby, M., El Desoky, S., Kari, J.A., Shril, S., Lienkamp, S.S., Barasch, J., Hildebrandt, F.
مصطلحات موضوعية: Cardiovascular and Metabolic Diseases
العلاقة: Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humans. Klämbt, V. and Werth, M. and Onuchic-Whitford, A.C. and Getwan, M. and Kitzler, T.M. and Buerger, F. and Mao, Y. and Deutsch, K. and Mann, N. and Majmundar, A.J. and Kaminski, M.M. and Shen, Tian and Schmidt-Ott, K.M. and Shalaby, M. and El Desoky, S. and Kari, J.A. and Shril, S. and Lienkamp, S.S. and Barasch, J. and Hildebrandt, F. Nephrology Dialysis Transplantation 36 (2): 237-246. February 2021
الإتاحة: https://doi.org/10.1093/ndt/gfaa215Test
http://edoc.mdc-berlin.de/19510Test/
https://edoc.mdc-berlin.de/19510Test/ -
6دورية أكاديمية
المؤلفون: Vivante, A., Mann, N., Yonath, H., Weiss, A.C., Getwan, M., Kaminski, M.M., Bohnenpoll, T., Teyssier, C., Chen, J., Shril, S., van der Ven, A.T., Ityel, H., Schmidt, J.M., Widmeier, E., Bauer, S.B., Sanna-Cherchi, S., Gharavi, A.G., Lu, W., Magen, D., Shukrun, R., Lifton, R.P., Tasic, V., Stanescu, H.C., Cavaillès, V., Kleta, R., Anikster, Y., Dekel, B., Kispert, A., Lienkamp, S.S., Hildebrandt, F.
مصطلحات موضوعية: Cardiovascular and Metabolic Diseases
العلاقة: A dominant mutation in nuclear receptor interacting protein 1 causes urinary tract malformations via dysregulation of retinoic acid signaling. Vivante, A. and Mann, N. and Yonath, H. and Weiss, A.C. and Getwan, M. and Kaminski, M.M. and Bohnenpoll, T. and Teyssier, C. and Chen, J. and Shril, S. and van der Ven, A.T. and Ityel, H. and Schmidt, J.M. and Widmeier, E. and Bauer, S.B. and Sanna-Cherchi, S. and Gharavi, A.G. and Lu, W. and Magen, D. and Shukrun, R. and Lifton, R.P. and Tasic, V. and Stanescu, H.C. and Cavaillès, V. and Kleta, R. and Anikster, Y. and Dekel, B. and Kispert, A. and Lienkamp, S.S. and Hildebrandt, F. Journal of the American Society of Nephrology 28 (8): 2364-2376. August 2017
الإتاحة: https://doi.org/10.1681/ASN.2016060694Test
http://edoc.mdc-berlin.de/18760Test/
https://edoc.mdc-berlin.de/18760Test/ -
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المؤلفون: Getwan, Maike
المساهمون: Blum, Martin
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المؤلفون: Blum, Martin, Getwan, Maike