Zobrazeno 1 - 10
of 76
pro vyhledávání: '"RFX3"'
Autor:
Chen, Baoen, Niu, Jixiao, Kreuzer, Johannes, Zheng, Baohui, Jarugumilli, Gopala K., Haas, Wilhelm, Wu, Xu
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2018 Sep 01. 115(36), E8403-E8412.
Externí odkaz:
https://www.jstor.org/stable/26531240
Autor:
Masayuki Sakiyama, Hirotaka Matsuo, Hirofumi Nakaoka, Yusuke Kawamura, Makoto Kawaguchi, Toshihide Higashino, Akiyoshi Nakayama, Airi Akashi, Jun Ueyama, Takaaki Kondo, Kenji Wakai, Yutaka Sakurai, Ken Yamamoto, Hiroshi Ooyama, Nariyoshi Shinomiya
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract Background Gout is a common disease resulting from hyperuricemia which causes acute arthritis. A recent genome-wide association study (GWAS) of gout identified three new loci for gout in Han Chinese: regulatory factor X3 (RFX3), potassium vo
Externí odkaz:
https://doaj.org/article/3fdd0a2def0c4ba9a6ed1afd843b8632
Akademický článek
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Autor:
Xinke Zhang, Jiakai Li, Jinglu Wang, Luwen Zhang, Guixiang Qi, Yihua Zhang, Pengxiu Dai, Yijing Chen
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
The transdifferentiation of adipose-derived mesenchymal stem cells (ADMSCs) into insulin-producing cells (IPCs) is a potential resource for the treatment of diabetes. However, the changes of genes and metabolic pathways on the transdifferentiation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1085f285e4a876f95e66707caef3d118
http://europepmc.org/articles/PMC8273515
http://europepmc.org/articles/PMC8273515
Akademický článek
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Autor:
Remi Robert, Dan Goldowitz, Hideya Kawaji, Wyeth W. Wasserman, Peter G. Zhang, Erik Arner, Yoshihide Hayashizaki, Carsten O. Daub, Sujin Im, Timo Lassmann, Thomas J. Ha, Alistair R. R. Forrest, Anthony Mathelier, Joanna Yeung, Masayoshi Itoh, Douglas J. Swanson, Piero Carninci
Publikováno v:
BMC Genomics
BMC Genomics, Vol 20, Iss 1, Pp 1-17 (2019)
BMC Genomics, Vol 20, Iss 1, Pp 1-17 (2019)
BackgroundThe work of the FANTOM5 Consortium has brought forth a new level of understanding of the regulation of gene transcription and the cellular processes involved in creating diversity of cell types. In this study, we extended the analysis of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c21f23bc0f3a633e83b679ca39eb21c0
http://europepmc.org/articles/PMC6751898
http://europepmc.org/articles/PMC6751898
Autor:
Tomi L. Toler, Timothy W. Yu, William B. Dobyns, Marcia C. Willing, Karen W. Gripp, Rolph Pfundt, Muhammad Iqbal, Xiadong Wang, Lance H. Rodan, Ada Hamosh, Cynthia S. Gubbels, Janice Baker, Thatjana Gardeitchik, Jenny Lai, André Reis, Fleur Vansenne, Jennifer E. Posey, Paranchai Boonsawat, Mathilde Nizon, Sébastien Küry, Jill R. Murrell, Julian L. Ambrus, Yunhong Wu, Laura A. Baker, Aubrie Soucy, Severine Audebert-Bellanger, Ellen van Binsbergen, Thomas Courtin, Guiseppe Zampino, Caleb P. Bupp, Holly K. Harris, Alan H. Beggs, Giulia Pascolini, Catharina (Nienke) M.L. Volker-Touw, Bert B.A. de Vries, Casie A. Genetti, La Donna L. Immken, Paola Grammatico, Martin Jakob Larsen, Sylvia Redon, Kévin Uguen, Reza Asadollahi, Madeleine Fannemel, Catherine Buchanan, Boris Keren, George E. Tiller, Lilian L. Cohen, Tojo Nakayama, Laurence E. Walsh, Iqra Ghulam Rasool, Audrey Labalme, Koen L.I. van Gassen, Pankaj B. Agrawal, Boxun Zhao, Gaetan Lesca, Steffan Syrbe, Kimberly A. Aldinger, Emanuele Agolini, Maria Kibaek, Muhammad Yasir Zahoor, Peter D. Turnpenny, Antonio Novelli, Ines Brösse, Claude Férec, Jorune Balciuniene, Nikoleta Argyrou, Victoria Suslovitch, Alice Poisson, Anita Rauch, Katelyn Payne, Christina Fagerberg, Cyril Mignot, Christopher Gray, Anne Blomhoff, Carolyn D. Applegate, Cornelia Kraus, Rami Abou Jamra, Marleen Simon, Martin Broly, Cara M. Skraban, Emily Fassi
Publikováno v:
Genetics in Medicine, 23(6), 1028-1040. Nature Publishing Group
Genetics in Medicine, 23, 6, pp. 1028-1040
Genetics in Medicine, 23, 1028-1040
Genet Med
Harris, H K, Nakayama, T, Lai, J, Zhao, B, Argyrou, N, Gubbels, C S, Soucy, A, Genetti, C A, Suslovitch, V, Rodan, L H, Tiller, G E, Lesca, G, Gripp, K W, Asadollahi, R, Hamosh, A, Applegate, C D, Turnpenny, P D, Simon, M E H, Volker-Touw, C M L, Gassen, K L I V, Binsbergen, E V, Pfundt, R, Gardeitchik, T, Vries, B B A D, Immken, L L, Buchanan, C, Willing, M, Toler, T L, Fassi, E, Baker, L, Vansenne, F, Wang, X, Ambrus, J L, Fannemel, M, Posey, J E, Agolini, E, Novelli, A, Rauch, A, Boonsawat, P, Fagerberg, C R, Larsen, M J, Kibaek, M, Labalme, A, Poisson, A, Payne, K K, Walsh, L E, Aldinger, K A, Balciuniene, J, Skraban, C, Gray, C, Murrell, J, Bupp, C P, Pascolini, G, Grammatico, P, Broly, M, Küry, S, Nizon, M, Rasool, I G, Zahoor, M Y, Kraus, C, Reis, A, Iqbal, M, Uguen, K, Audebert-Bellanger, S, Ferec, C, Redon, S, Baker, J, Wu, Y, Zampino, G, Syrbe, S, Brosse, I, Jamra, R A, Dobyns, W B, Cohen, L L, Blomhoff, A, Mignot, C, Keren, B, Courtin, T, Agrawal, P B, Beggs, A H & Yu, T W 2021, ' Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 23, no. 6, pp. 1028-1040 . https://doi.org/10.1038/s41436-021-01114-z
Genetics in Medicine, 23, 6, pp. 1028-1040
Genetics in Medicine, 23, 1028-1040
Genet Med
Harris, H K, Nakayama, T, Lai, J, Zhao, B, Argyrou, N, Gubbels, C S, Soucy, A, Genetti, C A, Suslovitch, V, Rodan, L H, Tiller, G E, Lesca, G, Gripp, K W, Asadollahi, R, Hamosh, A, Applegate, C D, Turnpenny, P D, Simon, M E H, Volker-Touw, C M L, Gassen, K L I V, Binsbergen, E V, Pfundt, R, Gardeitchik, T, Vries, B B A D, Immken, L L, Buchanan, C, Willing, M, Toler, T L, Fassi, E, Baker, L, Vansenne, F, Wang, X, Ambrus, J L, Fannemel, M, Posey, J E, Agolini, E, Novelli, A, Rauch, A, Boonsawat, P, Fagerberg, C R, Larsen, M J, Kibaek, M, Labalme, A, Poisson, A, Payne, K K, Walsh, L E, Aldinger, K A, Balciuniene, J, Skraban, C, Gray, C, Murrell, J, Bupp, C P, Pascolini, G, Grammatico, P, Broly, M, Küry, S, Nizon, M, Rasool, I G, Zahoor, M Y, Kraus, C, Reis, A, Iqbal, M, Uguen, K, Audebert-Bellanger, S, Ferec, C, Redon, S, Baker, J, Wu, Y, Zampino, G, Syrbe, S, Brosse, I, Jamra, R A, Dobyns, W B, Cohen, L L, Blomhoff, A, Mignot, C, Keren, B, Courtin, T, Agrawal, P B, Beggs, A H & Yu, T W 2021, ' Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 23, no. 6, pp. 1028-1040 . https://doi.org/10.1038/s41436-021-01114-z
Contains fulltext : 234024.pdf (Publisher’s version ) (Closed access) PURPOSE: We describe a novel neurobehavioral phenotype of autism spectrum disorder (ASD), intellectual disability, and/or attention-deficit/hyperactivity disorder (ADHD) associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fd06b954fdd324175d081fa359a3761
http://hdl.handle.net/11573/1523877
http://hdl.handle.net/11573/1523877
Autor:
Yong Zhang, Bénédicte Durand, Marie Paschaki, Michael J. Holtzman, Walter Reith, Sylvain Lemeille, Laurette Morlé, Dominique Baas, Joëlle Thomas, Jean-Luc Duteyrat, W. Stephen Kistler, Julie Jerber, Fabien Soulavie, Emmanuèle Barras, Aouatef Ait-Lounis
Publikováno v:
Nucleic Acids Research
Cilia assembly is under strict transcriptional control during animal development. In vertebrates, a hierarchy of transcription factors (TFs) are involved in controlling the specification, differentiation and function of multiciliated epithelia. RFX T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63ea6bd39f86ce41ed87fd4fb165eb8a
https://pubmed.ncbi.nlm.nih.gov/32725242
https://pubmed.ncbi.nlm.nih.gov/32725242
Akademický článek
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Publikováno v:
Molecular Biology and Evolution
The GLIS family transcription factors, GLIS1 and GLIS3, potentiate generation of induced pluripotent stem cells (iPSCs). In contrast, another GLIS family member, GLIS2, suppresses cell reprograming. To understand how these disparate roles arose, we e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57614a87336dbd7ac1170a01cb381d3c
https://pubmed.ncbi.nlm.nih.gov/31504761
https://pubmed.ncbi.nlm.nih.gov/31504761