Bjoern Schwer
Affiliations: | Harvard Medical School - Boston Children's Hospital | ||
| University of California, San Francisco, San Francisco, CA |
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"Bjoern Schwer"Mean distance: 16.63 (cluster 31) | S | N | B | C | P |
Parents
Sign in to add mentor| Harald zur Hausen | grad student | (Cell & Gene Therapy Tree) | |
| Frederick W. Alt | post-doc | ||
| Eric Verdin | post-doc |
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Publications
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| Dai HQ, Liang Z, Chang AN, et al. (2020) Direct analysis of brain phenotypes via neural blastocyst complementation. Nature Protocols |
| Chang AN, Liang Z, Dai HQ, et al. (2018) Neural blastocyst complementation enables mouse forebrain organogenesis. Nature |
| Alt FW, Schwer B. (2018) DNA double-strand breaks as drivers of neural genomic change, function, and disease. Dna Repair |
| Wei PC, Lee CS, Du Z, et al. (2018) Three classes of recurrent DNA break clusters in brain progenitors identified by 3D proximity-based break joining assay. Proceedings of the National Academy of Sciences of the United States of America |
| Wood JG, Schwer B, Wickremesinghe PC, et al. (2018) Sirt4 is a mitochondrial regulator of metabolism and lifespan in Drosophila melanogaster. Proceedings of the National Academy of Sciences of the United States of America |
| Schwer B, Wei PC, Chang AN, et al. (2016) Transcription-associated processes cause DNA double-strand breaks and translocations in neural stem/progenitor cells. Proceedings of the National Academy of Sciences of the United States of America. 113: 2258-63 |
| Wei PC, Chang AN, Kao J, et al. (2016) Long Neural Genes Harbor Recurrent DNA Break Clusters in Neural Stem/Progenitor Cells. Cell. 164: 644-55 |
| Gostissa M, Schwer B, Chang A, et al. (2014) IgH class switching exploits a general property of two DNA breaks to be joined in cis over long chromosomal distances. Proceedings of the National Academy of Sciences of the United States of America. 111: 2644-9 |
| Khongkow M, Olmos Y, Gong C, et al. (2013) SIRT6 modulates paclitaxel and epirubicin resistance and survival in breast cancer. Carcinogenesis. 34: 1476-86 |
| Shi W, Bain AL, Schwer B, et al. (2013) Essential developmental, genomic stability, and tumour suppressor functions of the mouse orthologue of hSSB1/NABP2. Plos Genetics. 9: e1003298 |