Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Theresa Mair"'
Autor:
Anna Kostecka, Tomasz Nowikiewicz, Paweł Olszewski, Magdalena Koczkowska, Monika Horbacz, Monika Heinzl, Maria Andreou, Renato Salazar, Theresa Mair, Piotr Madanecki, Magdalena Gucwa, Hanna Davies, Jarosław Skokowski, Patrick G. Buckley, Rafał Pęksa, Ewa Śrutek, Łukasz Szylberg, Johan Hartman, Michał Jankowski, Wojciech Zegarski, Irene Tiemann-Boege, Jan P. Dumanski, Arkadiusz Piotrowski
Publikováno v:
npj Breast Cancer, Vol 8, Iss 1, Pp 1-10 (2022)
Abstract The mammary gland undergoes hormonally stimulated cycles of proliferation, lactation, and involution. We hypothesized that these factors increase the mutational burden in glandular tissue and may explain high cancer incidence rate in the gen
Externí odkaz:
https://doaj.org/article/cc2598149fc04588ac0c210c85b15585
Autor:
Theresa Mair, Maja Ivankovic, Christian Paar, Helmut J. F. Salzer, Angelika Heissl, Bernd Lamprecht, Elisabeth Schreier-Lechner, Irene Tiemann-Boege
Publikováno v:
Viruses, Vol 13, Iss 9, p 1712 (2021)
The SARS-CoV-2 pandemic has required the development of multiple testing systems to monitor and control the viral infection. Here, we developed a PCR test to screen COVID-19 infections that can process up to ~180 samples per day without the requireme
Externí odkaz:
https://doaj.org/article/948e6b0bfb4041e28aa623130664184f
Autor:
Sofia Moura, Ingrid Hartl, Atena Yasari, Veronika Brumovska, Yasmin Striedner, Marina Bishara, Theresa Mair, Thomas Ebner, Gerhard J. Schütz, Eva Sevcsik, Irene Tiemann-Boege
Delayed fatherhood results in a higher risk to inherit a new germline mutation that might result in a congenital disorder in the offspring. In particular, some FGFR3 mutations increase in frequency with age, but there are still a large number of unch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::875cf5f30ab43faf85a7764db57f7022
https://doi.org/10.1101/2022.07.31.502216
https://doi.org/10.1101/2022.07.31.502216
Publikováno v:
The Febs Journal
Gain‐of‐function mutations in the receptor tyrosine kinase pathway are often lethal; yet, it might be tolerated at very low frequencies as postzygotic mosaics resulting in a vast range of new phenotypes, unknown before the detection of the mosaic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dc74ef1f66c45d347fcd931757572fe
https://doi.org/10.1111/febs.15528
https://doi.org/10.1111/febs.15528
Autor:
M. Koczkowska, Paweł Olszewski, Hanna Davies, Johan Hartman, Theresa Mair, M. Andreou, M. Horbacz, A. Kostecka, Piotr Madanecki, P. G. Buckley, Jan P. Dumanski, Ewa Srutek, Magdalena Gucwa, Michał Jankowski, Tomasz Nowikiewicz, Renato Salazar, Jarosław Skokowski, L. Szylberg, Monika Heinzl, Irene Tiemann-Boege, Arkadiusz Piotrowski, Wojciech Zegarski, Rafał Pęksa
The mammary gland undergoes hormonally stimulated cycles of proliferation, lactation and involution. We hypothesized that these factors increase the mutational burden in glandular tissue and may explain high cancer incidence rate in the general popul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32606bae6d238402262d47fd3e6583b2
https://doi.org/10.1101/2021.09.27.21263863
https://doi.org/10.1101/2021.09.27.21263863
Autor:
Thomas Ebner, Hartl I, Angelika Heissl, Monika Heinzl, Moura S, Barbara Arbeithuber, Pröll J, Irene Tiemann-Boege, Ivankovic M, Shebl O, Theresa Mair, Renato Salazar
De novo mutations (DNMs) are an important player in heritable diseases and evolution, yet little is known about the different mutagenic processes in our germline given the difficulty to reliably identify ultra-low frequency variants. Of particular in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9260be78c7f4dfc4c856d82d3d172df
https://doi.org/10.1101/2021.04.26.441422
https://doi.org/10.1101/2021.04.26.441422
Autor:
Renato Salazar, Barbara Arbeithuber, Maja Ivankovic, Monika Heinzl, Sofia Moura, Ingrid Hartl, Theresa Mair, Angelika Lahnsteiner, Thomas Ebner, Omar Shebl, Johannes Pröll, Irene Tiemann-Boege
Publikováno v:
Genome research. 32(3)
De novo mutations (DNMs) are important players in heritable diseases and evolution. Of particular interest are highly recurrent DNMs associated with congenital disorders that have been described as selfish mutations expanding in the male germline, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7ff4e8f34ebdf7de69fbef36e403fa0
https://pubmed.ncbi.nlm.nih.gov/35210354
https://pubmed.ncbi.nlm.nih.gov/35210354