Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maria Luisa Amaral"'
Autor:
Sudha Sunil Rajderkar, Kitt Paraiso, Maria Luisa Amaral, Michael Kosicki, Laura E. Cook, Fabrice Darbellay, Cailyn H. Spurrell, Marco Osterwalder, Yiwen Zhu, Han Wu, Sarah Yasmeen Afzal, Matthew J. Blow, Guy Kelman, Iros Barozzi, Yoko Fukuda-Yuzawa, Jennifer A. Akiyama, Veena Afzal, Stella Tran, Ingrid Plajzer-Frick, Catherine S. Novak, Momoe Kato, Riana D. Hunter, Kianna von Maydell, Allen Wang, Lin Lin, Sebastian Preissl, Steven Lisgo, Bing Ren, Diane E. Dickel, Len A. Pennacchio, Axel Visel
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract The genetic basis of human facial variation and craniofacial birth defects remains poorly understood. Distant-acting transcriptional enhancers control the fine-tuned spatiotemporal expression of genes during critical stages of craniofacial d
Externí odkaz:
https://doaj.org/article/ad066eccb027472d812a541544ff79a2
Publikováno v:
BMC Bioinformatics, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract Background Microarray experiments comprise more than half of all series in the Gene Expression Omnibus (GEO). However, downloading and analyzing raw or semi-processed microarray data from GEO is not intuitive and requires manual error-prone
Externí odkaz:
https://doaj.org/article/036a03ab82384c44b4b5800bbe249b20
Autor:
Timothy W R Kelso, Devin K Porter, Maria Luisa Amaral, Maxim N Shokhirev, Christopher Benner, Diana C Hargreaves
Publikováno v:
eLife, Vol 6 (2017)
ARID1A, a subunit of the SWI/SNF chromatin remodeling complex, is frequently mutated in cancer. Deficiency in its homolog ARID1B is synthetically lethal with ARID1A mutation. However, the functional relationship between these homologs has not been ex
Externí odkaz:
https://doaj.org/article/a449aac1fa7744e5be6b531a3542b1b7
Autor:
Yanxiao Zhang, Maria Luisa Amaral, Chenxu Zhu, Steven Francis Grieco, Xiaomeng Hou, Lin Lin, Justin Buchanan, Liqi Tong, Sebastian Preissl, Xiangmin Xu, Bing Ren
Publikováno v:
Cell research, vol 32, iss 11
Loss of heterochromatin has been implicated as a cause of pre-mature aging and age-associated decline in organ functions in mammals; however, the specific cell types and gene loci affected by this type of epigenetic change have remained unclear. To a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f55084e23efdea58617cbc19ee5c7ff7
https://pubmed.ncbi.nlm.nih.gov/36207411
https://pubmed.ncbi.nlm.nih.gov/36207411
Autor:
Sora Chee, Juan Carlos Izpisua Belmonte, Eugin Destici, Quan Zhu, Elie Farah, Rongxin Fang, Bing Ren, Sylvia M. Evans, Hui Huang, Sebastian Preissl, Jun Wu, Kaiyue Ma, Yanxiao Zhang, Rong Hu, Zhen Ye, Leqian Yu, Maria Luisa Amaral, Ah Young Lee, Yunjiang Qiu, Ting Li, Jonathan D. Grinstein, Neil C. Chi
Publikováno v:
Nature genetics, vol 51, iss 9
Nature genetics
Nature genetics
Chromatin architecture has been implicated in cell type-specific gene regulatory programs, yet how chromatin remodels during development remains to be fully elucidated. Here, by interrogating chromatin reorganization during human pluripotent stem cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ad05b18d879b139bae248d20d0446ab
https://escholarship.org/uc/item/1q9817wd
https://escholarship.org/uc/item/1q9817wd
Publikováno v:
BMC Bioinformatics
BMC Bioinformatics, Vol 19, Iss 1, Pp 1-6 (2018)
BMC Bioinformatics, Vol 19, Iss 1, Pp 1-6 (2018)
Microarray experiments comprise more than half of all series in the Gene Expression Omnibus (GEO). However, downloading and analyzing raw or semi-processed microarray data from GEO is not intuitive and requires manual error-prone analysis and a bioin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f4d080f23e378efe75effea6605aa8
https://doi.org/10.1186/s12859-018-2308-x
https://doi.org/10.1186/s12859-018-2308-x
Autor:
Christopher Benner, Diana C. Hargreaves, Timothy W. R. Kelso, Maria Luisa Amaral, Maxim N. Shokhirev, Devin K. Porter
Publikováno v:
eLife
eLife, Vol 6 (2017)
eLife, Vol 6 (2017)
ARID1A, a subunit of the SWI/SNF chromatin remodeling complex, is frequently mutated in cancer. Deficiency in its homolog ARID1B is synthetically lethal with ARID1A mutation. However, the functional relationship between these homologs has not been ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803583a880be6ed706e72f765a0c7d75
https://pubmed.ncbi.nlm.nih.gov/28967863
https://pubmed.ncbi.nlm.nih.gov/28967863