Researcher Portfolio

 
   

Krastev, Dragomir

Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society  

 

Researcher Profile

 
Position: Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society
Researcher ID: https://pure.mpg.de/cone/persons/resource/persons219341

External references

 
WorldCat Search for Krastev, Dragomir
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Publications

 
 
 : Aleksandrov, R., Dotchev, A., Poser, I., Krastev, D., Georgiev, G., Panova, G. C., Babukov, Y., Danovski, G., Dyankova, T., Hubatsch, L., Ivanova, A., Atemin, A., Nedelcheva-Veleva, M. N., Hasse, S., Sarov, M., Buchholz, F., Hyman, A., Grill, S. W., & Stoynov, S. (2018). Protein Dynamics in Complex DNA Lesions. Molecular cell, 69(6), 1046-1061. doi:10.1016/j.molcel.2018.02.016. [PubMan] : Kappei, D., Butter, F., Benda, C., Scheibe, M., Draskovic, I., Stevense, M., Novo, C. L., Basquin, C., Araki, M., Araki, K., Krastev, D., Kittler, R., Jessberger, R., Londoño-Vallejo, J. A., Mann, M., & Buchholz, F. (2013). HOT1 is a mammalian direct telomere repeat-binding protein contributing to telomerase recruitment. The EMBO Journal, 32(12), 1681-1701. [PubMan] : Krastev, D., Slabicki, M., Paszkowski-Rogacz, M., Hubner, N. C., Junqueira, M., Shevchenko, A., Mann, M., Neugebauer, K. M., & Buchholz, F. (2011). A systematic RNAi synthetic interaction screen reveals a link between p53 and snoRNP assembly. Nature Cell Biology, 13(7), 809-818. [PubMan] : Gospodinov, A., Vaissiere, T., Krastev, D., Legube, G., Anachkova, B., & Herceg, Z. (2011). Mammalian Ino80 mediates double-strand break repair through its role in DNA end strand resection. Molecular and Cellular Biology, 31(23), 4735-4745. [PubMan] : Krastev, D., & Buchholz, F. (2011). Ribosome biogenesis and p53 who is regulating who? Cell Cycle (Georgetown, Tex.), 10(20), 3417-3418. [PubMan] : Slabicki, M., Theis, M., Krastev, D., Samsonov, S., Mundwiller, E., Junqueira, M., Paszkowski-Rogacz, M., Teyra, J., Heninger, A.-K., Poser, I., Prieur, F., Truchetto, J., Confavreux, C., Marelli, C., Durr, A., Camdessanche, J. P., Brice, A., Shevchenko, A., Pisabarro, M. T., Stevanin, G., & Buchholz, F. (2010). A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia. PLoS Biology, 8(6): e1000408. [PubMan] : Krastev, D. (2009). An RNA interference synthetic interaction screen identifies vulnerability factors for TP53 mutant cells. PhD Thesis, Technische Universitaet Dresden, Dresden. [PubMan]