Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Benaglio, Paola"'
Autor:
Benaglio, Paola, Zhu, Han, Okino, Mei-Lin, Yan, Jian, Elgamal, Ruth, Nariai, Naoki, Beebe, Elisha, Korgaonkar, Katha, Qiu, Yunjiang, Donovan, Margaret K.R., Chiou, Joshua, Wang, Gaowei, Newsome, Jacklyn, Kaur, Jaspreet, Miller, Michael, Preissl, Sebastian, Corban, Sierra, Aylward, Anthony, Taipale, Jussi, Ren, Bing, Frazer, Kelly A., Sander, Maike, Gaulton, Kyle J.
Publikováno v:
In Cell Genomics 14 December 2022 2(12)
Akademický článek
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Autor:
Benaglio, Paola1 (AUTHOR), Newsome, Jacklyn2 (AUTHOR), Han, Jee Yun3 (AUTHOR), Chiou, Joshua4 (AUTHOR), Aylward, Anthony2 (AUTHOR), Corban, Sierra1 (AUTHOR), Miller, Michael3 (AUTHOR), Okino, Mei-Lin1 (AUTHOR), Kaur, Jaspreet1 (AUTHOR), Preissl, Sebastian3 (AUTHOR), Gorkin, David U.3 (AUTHOR), Gaulton, Kyle J.1 (AUTHOR) kgaulton@ucsd.edu
Publikováno v:
PLoS Genetics. 6/8/2023, Vol. 19 Issue 6, p1-28. 28p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Elgamal, Ruth M, Kudtarkar, Parul, Melton, Rebecca L, Mummey, Hannah M, Benaglio, Paola, Okino, Mei-Lin, Gaulton, Kyle J
Publikováno v:
bioRxiv
Pancreatic islets are comprised of multiple endocrine cell types that produce hormones required for glucose homeostasis, and islet dysfunction is a major factor in the development of type 1 and type 2 diabetes (T1D, T2D). Numerous studies have genera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdf56bbcf632e7c7b4ded701330e6f31
https://doi.org/10.1101/2023.02.03.526994
https://doi.org/10.1101/2023.02.03.526994
Autor:
Secchi, Christian1 (AUTHOR) chsecchi@health.ucsd.edu, Benaglio, Paola2 (AUTHOR), Mulas, Francesca2 (AUTHOR), Belli, Martina1 (AUTHOR), Stupack, Dwayne1 (AUTHOR), Shimasaki, Shunichi1 (AUTHOR)
Publikováno v:
Journal of Translational Medicine. 2/27/2021, Vol. 19 Issue 1, p1-15. 15p.
Autor:
D'Antonio, Matteo, Nguyen, Jennifer P., Arthur, Timothy D., Arias, Angelo D., Benaglio, Paola, Berggren, W. Travis, Borja, Victor, Belmonte, Juan Carlos Izpisua, Cook, Megan, DeBoever, Christopher, Diffenderfer, Kenneth E., Donovan, Margaret K. R., Farnam, KathyJean, Frazer, Kelly A., Fujita, Kyohei, Garcia, Melvin, Harismendy, Olivier, Henson, Benjamin A., Jakubosky, David, Jepsen, Kristen
Publikováno v:
Nature Communications; 7/21/2023, Vol. 14 Issue 1, p1-18, 18p
Autor:
Nishiguchi, Koji M., Tearle, Richard G., Liu, Yangfan P., Oh, Edwin C., Miyake, Noriko, Benaglio, Paola, Harper, Shyana, Koskiniemi-Kuendig, Hanna, Venturini, Giulia, Sharon, Dror, Koenekoop, Robert K., Nakamura, Makoto, Kondo, Mineo, Ueno, Shinji, Yasuma, Tetsuhiro R., Beckmann, Jacques S., Ikegawa, Shiro, Matsumoto, Naomichi, Terasaki, Hiroko, Berson, Eliot L., Katsanis, Nicholas, Rivolta, Carlo
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2013 Oct 01. 110(40), 16139-16144.
Externí odkaz:
https://www.jstor.org/stable/23749726
Autor:
Yan, Jian, Qiu, Yunjiang, Ribeiro Dos Santos, André M, Yin, Yimeng, Li, Yang E, Vinckier, Nick, Nariai, Naoki, Benaglio, Paola, Raman, Anugraha, Li, Xiaoyu, Fan, Shicai, Chiou, Joshua, Chen, Fulin, Frazer, Kelly A, Gaulton, Kyle J, Sander, Maike, Taipale, Jussi, Ren, Bing
Publikováno v:
Nature, vol 591, iss 7848
Many sequence variants have been linked to complex human traits and diseases1, but deciphering their biological functions remains challenging, as most of them reside in noncoding DNA. Here we have systematically assessed the binding of 270 human tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::1c1864bb841ef387e3f3d3de0ed4b195
https://escholarship.org/uc/item/22x9z92w
https://escholarship.org/uc/item/22x9z92w
Autor:
Yan, Jian, Qiu, Yunjiang, Ribeiro dos Santos, André M, Yin, Yimeng, Li, Yang E., Vinckier, Nick, Nariai, Naoki, Benaglio, Paola, Raman, Anugraha, Li, Xiaoyu, Fan, Shicai, Chiou, Joshua, Chen, Fulin, Frazer, Kelly A., Gaulton, Kyle J., Sander, Maike, Taipale, Jussi, Ren, Bing
Publikováno v:
Nature
A large number of sequence variants have been linked to complex human traits and diseases(1), but deciphering their biological functions is still challenging since most of them reside in the noncoding DNA. To fill this gap, we have systematically ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::354d3888b071ef9ac1b7b3df3d87a00d
https://europepmc.org/articles/PMC9367673/
https://europepmc.org/articles/PMC9367673/