Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lili Hegedus"'
Autor:
Lili Hegedus, Agnes Toth, Gabor M. Harami, Janos Palinkas, Nargis Karatayeva, Eniko Sajben-Nagy, Szabolcs Bene, Sara Afzali Jaktajdinani, Mihaly Kovacs, Szilvia Juhasz, Peter Burkovics
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Genome replication is frequently impeded by highly stable DNA secondary structures, including G-quadruplex (G4) DNA, that can hinder the progression of the replication fork. Human WRNIP1 (Werner helicase Interacting Protein 1) associates wit
Externí odkaz:
https://doaj.org/article/ef8693911000466fb2cdcfe50eeb72f6
Autor:
Min Peng, Ke Cong, Nicholas J. Panzarino, Sumeet Nayak, Jennifer Calvo, Bin Deng, Lihua Julie Zhu, Monika Morocz, Lili Hegedus, Lajos Haracska, Sharon B. Cantor
Publikováno v:
Cell Reports, Vol 24, Iss 12, Pp 3251-3261 (2018)
Summary: The DNA helicase FANCJ is mutated in hereditary breast and ovarian cancer and Fanconi anemia (FA). Nevertheless, how loss of FANCJ translates to disease pathogenesis remains unclear. We addressed this question by analyzing proteins associate
Externí odkaz:
https://doaj.org/article/935ddf6285564b53bbb87c4cac17d059
Autor:
Csilla Brasko, Kevin Smith, Csaba Molnar, Nora Farago, Lili Hegedus, Arpad Balind, Tamas Balassa, Abel Szkalisity, Farkas Sukosd, Katalin Kocsis, Balazs Balint, Lassi Paavolainen, Marton Z. Enyedi, Istvan Nagy, Laszlo G. Puskas, Lajos Haracska, Gabor Tamas, Peter Horvath
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-7 (2018)
The isolation of single cells while retaining context is important for quantifying cellular heterogeneity but technically challenging. Here, the authors develop a high-throughput, scalable workflow for microscopy-based single cell isolation using mac
Externí odkaz:
https://doaj.org/article/45fa759495a24fc3831e7ab0ebc0ea21
Autor:
Mónika Mórocz, Sumeet Nayak, Nicholas J. Panzarino, Min Peng, Ke Cong, Sharon B. Cantor, Lihua Julie Zhu, Jennifer A. Calvo, Bin Deng, Lajos Haracska, Lili Hegedus
Publikováno v:
Cell reports
Cell Reports, Vol 24, Iss 12, Pp 3251-3261 (2018)
Cell Reports, Vol 24, Iss 12, Pp 3251-3261 (2018)
SUMMARY The DNA helicase FANCJ is mutated in hereditary breast and ovarian cancer and Fanconi anemia (FA). Nevertheless, how loss of FANCJ translates to disease pathogenesis remains unclear. We addressed this question by analyzing proteins associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebcf8b438170c39e2b1a7dd7aee7a293
https://pubmed.ncbi.nlm.nih.gov/30232006
https://pubmed.ncbi.nlm.nih.gov/30232006