Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Chelsea Ray"'
Publikováno v:
Stem Cell Research, Vol 16, Iss 2, Pp 252-255 (2016)
Parental origin-dependent expression of the imprinted genes is essential for mammalian development. Zfp57 maintains genomic imprinting in mouse embryos and ES cells. To examine the allelic expression patterns of the imprinted genes in ES cells, we ob
Externí odkaz:
https://doaj.org/article/291ef4cc05c3418ebacef18778dbcf5f
Autor:
Lizhi Liu, Shi-Qing Mao, Chelsea Ray, Yu Zhang, Fong T. Bell, Sheau-Fang Ng, Guo-Liang Xu, Xiajun Li
Publikováno v:
Stem Cell Research, Vol 15, Iss 2, Pp 435-443 (2015)
TET proteins have been found to play an important role in active demethylation at CpG sites in mammals. There are some reports implicating their functions in removal of DNA methylation imprint at the imprinted regions in the germline. However, it is
Externí odkaz:
https://doaj.org/article/6d8f02cc03004a0580a887e4e35bae81
Autor:
Natalie Clifford Barney, Chelsea Ray
This long-lost novel recounts a passionate triangle of love and loss among three of the most daring women of belle époque Paris. In this barely disguised roman à clef, the legendary American heiress, writer, and arts patron Natalie Clifford Barney,
Autor:
Chelsea Ray
Publikováno v:
Women in French Studies. 30:154-169
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec513d33777a2307e3d28c9397ba96e4
https://doi.org/10.1353/wfs.2022.0012
https://doi.org/10.1353/wfs.2022.0012
Autor:
Chelsea Ray
Publikováno v:
Horrible Mothers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de83f4b28ca4e93f74c0383937969599
https://doi.org/10.2307/j.ctvr0qt7n.7
https://doi.org/10.2307/j.ctvr0qt7n.7
Publikováno v:
Stem Cell Research, Vol 16, Iss 2, Pp 252-255 (2016)
Parental origin-dependent expression of the imprinted genes is essential for mammalian development. Zfp57 maintains genomic imprinting in mouse embryos and ES cells. To examine the allelic expression patterns of the imprinted genes in ES cells, we ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66a13a474a10f4ec31c41849ca0f5203
https://doi.org/10.1016/j.scr.2016.01.017
https://doi.org/10.1016/j.scr.2016.01.017
Publikováno v:
Epigenetics. 8:1268-1279
Genomic imprinting is a common epigenetic phenomenon in mammals. Dysregulation of genomic imprinting has been implicated in a variety of human diseases. ZFP57 is a master regulator in genomic imprinting. Loss of ZFP57 causes loss of DNA methylation i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b8229f914c9ac8dec16397e93663542
https://doi.org/10.4161/epi.26544
https://doi.org/10.4161/epi.26544
Publikováno v:
Stem Cell Research. 11:861-873
Derivation of induced pluripotent stem (iPS) cells is mainly an epigenetic reprogramming process. It is still quite controversial how genomic imprinting is reprogrammed in iPS cells. Thus, we derived multiple iPS clones from genetically identical mou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c0c6bbaec56fe447c78d4f8db0bb744
https://doi.org/10.1016/j.scr.2013.05.011
https://doi.org/10.1016/j.scr.2013.05.011
Autor:
Yu Zhang, Shi-Qing Mao, Chelsea Ray, Lizhi Liu, Sheau-Fang Ng, Xiajun Li, Fong T. Bell, Guoliang Xu
Publikováno v:
Stem Cell Research, Vol 15, Iss 2, Pp 435-443 (2015)
TET proteins have been found to play an important role in active demethylation at CpG sites in mammals. There are some reports implicating their functions in removal of DNA methylation imprint at the imprinted regions in the germline. However, it is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dcfe5b60ee5f3b7d2da518e7a7e346b
https://europepmc.org/articles/PMC4618460/
https://europepmc.org/articles/PMC4618460/
Autor:
Lizhi Liu, Xiao Yang, Sachiko Takikawa, Sheau-Fang Ng, Yulia Shamis, Xiajun Li, Chelsea Ray, Ivan P. Moskowitz, Fong T. Bell, Dana E. Cullen, Lijuan Xiao, Chen-Leng Cai, Guan Yang
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 112(16)
Zfp57 is a maternal–zygotic effect gene that maintains genomic imprinting. Here we report that Zfp57 mutants exhibited a variety of cardiac defects including atrial septal defect (ASD), ventricular septal defect (VSD), thin myocardium, and reduced
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bed0ad6415b3435214079de1a431c14f
https://pubmed.ncbi.nlm.nih.gov/25848000
https://pubmed.ncbi.nlm.nih.gov/25848000