Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Olazabal-Herrero A"'
Autor:
Boddu, Prajwal C., Gupta, Abhishek K., Roy, Rahul, De La Peña Avalos, Bárbara, Olazabal-Herrero, Anne, Neuenkirchen, Nils, Zimmer, Joshua T., Chandhok, Namrata S., King, Darren, Nannya, Yasuhito, Ogawa, Seishi, Lin, Haifan, Simon, Matthew D., Dray, Eloise, Kupfer, Gary M., Verma, Amit, Neugebauer, Karla M., Pillai, Manoj M.
Publikováno v:
In Molecular Cell 18 April 2024 84(8):1475-1495
Autor:
Olazabal-Herrero, Anne, He, Boxue, Kwon, Youngho, Gupta, Abhishek K., Dutta, Arijit, Huang, Yuxin, Boddu, Prajwal, Liang, Zhuobin, Liang, Fengshan, Teng, Yaqun, Lan, Li, Chen, Xiaoyong, Pei, Huadong, Pillai, Manoj M., Sung, Patrick, Kupfer, Gary M.
Publikováno v:
In Cell Reports 23 January 2024 43(1)
Autor:
Anne Olazabal-Herrero, Boxue He, Youngho Kwon, Abhishek K. Gupta, Arijit Dutta, Yuxin Huang, Prajwal Boddu, Zhuobin Liang, Fengshan Liang, Yaqun Teng, Li Lan, Xiaoyong Chen, Huadong Pei, Manoj M. Pillai, Patrick Sung, Gary M. Kupfer
Publikováno v:
Cell Reports, Vol 43, Iss 1, Pp 113610- (2024)
Summary: Fanconi anemia (FA) is characterized by congenital abnormalities, bone marrow failure, and cancer susceptibility. The central FA protein complex FANCI/FANCD2 (ID2) is activated by monoubiquitination and recruits DNA repair proteins for inter
Externí odkaz:
https://doaj.org/article/bc92b447e5014f469f04a528e03fd245
Autor:
T. J. Gonzalez-Lopez, S. Matarraz, I. Caparros, M. F. Lopez-Fernandez, M. E. Mingot-Castellano, A. Jimenez Martin, F. Fernandez-Fuertes, J. I. Sánchez Gallego, P. Leoz, B. Cuevas Ruiz, M. V. Cuevas Ruiz, C. Martin Marín, J. Olazabal Herrero, P. de Vicente Cámara, A. Orfao
Publikováno v:
HemaSphere, Vol 6, Pp 1528-1529 (2022)
Externí odkaz:
https://doaj.org/article/54e5242460ea4b64ae2efe794c2a9ceb
Publikováno v:
In European Journal of Cell Biology January 2019 98(1):12-26
Autor:
Olazabal‐Herrero, Anne1,2 (AUTHOR), Bilbao‐Arribas, Martin1 (AUTHOR), Carlevaris, Onintza3 (AUTHOR), Sendino, Maria1 (AUTHOR), Varela‐Martinez, Endika1 (AUTHOR), Jugo, Begoña M.1 (AUTHOR), Berra, Edurne3,4 (AUTHOR), Rodriguez, Jose Antonio1 (AUTHOR) josean.rodriguez@ehu.eus
Publikováno v:
FEBS Journal. Oct2021, Vol. 288 Issue 20, p5943-5963. 21p.
Autor:
Prajwal C Boddu, Abhishek Gupta, Rahul Roy, Barbara De La Pena Avalos, Ane Olazabal Herrero, Nils Neuenkirchen, Josh Zimmer, Namrata Chandhok, Darren King, Yashuhito Nannya, Seishi Ogawa, Haifan Lin, Matthew Simon, Eloise Dray, Gary Kupfer, Amit K. Verma, Karla M. Neugebauer, Manoj M Pillai
Publikováno v:
bioRxiv
Transcription and splicing of pre-messenger RNA are closely coordinated, but how this functional coupling is disrupted in human disease remains unexplored. Here, we investigated the impact of non-synonymous mutations in SF3B1 and U2AF1, two commonly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fc52bc1a58f7506bad42b4fd807506b
https://europepmc.org/articles/PMC9994134/
https://europepmc.org/articles/PMC9994134/
Autor:
Begoña M. Jugo, Maria Sendino, Edurne Berra, Onintza Carlevaris, Jose Antonio Rodriguez, Martin Bilbao-Arribas, Anne Olazabal-Herrero, Endika Varela-Martínez
Publikováno v:
The FEBS Journal. 288:5943-5963
Despite its potential clinical relevance, the product of the DMWD (dystrophia myotonica, WD repeat containing) gene is a largely uncharacterized protein. The DMWD amino acid sequence is similar to that of WDR20, a known regulator of the USP12 and USP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de8c431159cbb7b94ef02ec889753d60
https://doi.org/10.1111/febs.15875
https://doi.org/10.1111/febs.15875
Autor:
Anne Olazabal Herrero, Fengshan Liang, Arijit Dutta, Yuxin Huang, Zhuobin Liang, Abhishek K Gupta, Li Lan, Manoj M Pillai, Patrick Sung, Gary M. Kupfer
Publikováno v:
Blood. 140:5828-5829
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43eee37000d854c233353c238e412568
https://doi.org/10.1182/blood-2022-166798
https://doi.org/10.1182/blood-2022-166798
Autor:
Anne Olazabal-Herrero, Fengshan Liang, Arijit Dutta, Yuxin Huang, Zhuobin Liang, Abhishek Gupta, Yaqun Teng, Li Lan, Xiaoyong Chen, Huadong Pei, Manoj Pillai, Patrick Sung, Gary Kupfer
Publikováno v:
Cancer Research. 83:6100-6100
Background: Fanconi Anemia (FA) is a rare genetic disease characterized by bone marrow failure and cancer susceptibility. FA gene mutations are also widespread somatically in non-FA cancer patients. While the FA pathway participates in DNA repair, it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12a79c77743c0dc3840a6bcf5d874ae1
https://doi.org/10.1158/1538-7445.am2023-6100
https://doi.org/10.1158/1538-7445.am2023-6100