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VISITING ASSISTANT PROFESSOR | Genetics and Genomic Sciences
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Dive into the research topics where Detlev Schindler is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Disruption of the FA/BRCA pathway in bladder cancer
Neveling, K., Kalb, R., Florl, A. R., Herterich, S., Friedl, R., Hoehn, H., Hader, C., Hartmann, F. H., Nanda, I., Steinlein, C., Schmid, M., Tönnies, H., Hurst, C. D., Knowles, M. A., Hanenberg, H., Schulz, W. A. & Schindler, D., Nov 2007, In: Cytogenetic and Genome Research. 118, 2-4, p. 166-176 11 p.Research output: Contribution to journal › Article › peer-review
34 Scopus citations -
Inhibition of primordial germ cell proliferation by the medaka male determining gene Dmrt1bY
Herpin, A., Schindler, D., Kraiss, A., Hornung, U., Winkler, C. & Schartl, M., 2007, In: BMC Developmental Biology. 7, 99.Research output: Contribution to journal › Article › peer-review
Open Access58 Scopus citations -
Preface
Schindler, D. & Hoehn, H., 2007, Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging. Hoehn, H. & Schindler, D. (eds.). p. XI-XII (Monographs in Human Genetics; vol. 15).Research output: Chapter in Book/Report/Conference proceeding › Foreword/postscript
Open Access -
Radiation-induced DNA damage and repair in peripheral blood mononuclear cells from Nijmegen breakage syndrome patients and carriers assessed by the Comet assay
Bürger, S., Schindler, D., Fehn, M., Mühl, B., Mahrhofer, H., Flentje, M., Hoehn, H., Seemanová, E. & Djuzenova, C. S., May 2006, In: Environmental and Molecular Mutagenesis. 47, 4, p. 260-270 11 p.Research output: Contribution to journal › Article › peer-review
20 Scopus citations -
Spectral karyotyping of Werner syndrome fibroblast cultures
Melcher, R., Von Golitschek, R., Steinlein, C., Schindler, D., Neitzel, H., Kainer, K., Schmid, M. & Hoehn, H., 2000, In: Cytogenetics and Cell Genetics. 91, 1-4, p. 180-185 6 p.Research output: Contribution to journal › Article › peer-review
49 Scopus citations
Press/Media
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HMN 2025: How New gene is linked to extreme circumstances of Fanconi anemia
10/05/25
1 item of Media coverage
Press/Media
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