Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Montserrat C Anguera"'
Autor:
Camille M Syrett, Vishal Sindhava, Suchita Hodawadekar, Arpita Myles, Guanxiang Liang, Yue Zhang, Satabdi Nandi, Michael Cancro, Michael Atchison, Montserrat C Anguera
Publikováno v:
PLoS Genetics, Vol 13, Iss 10, p e1007050 (2017)
X-chromosome inactivation (XCI) in female lymphocytes is uniquely regulated, as the inactive X (Xi) chromosome lacks localized Xist RNA and heterochromatin modifications. Epigenetic profiling reveals that Xist RNA is lost from the Xi at the pro-B cel
Externí odkaz:
https://doaj.org/article/a693d497f5ad4372b8ec68f216f855e9
Autor:
Mengcheng Luo, Jian Zhou, N Adrian Leu, Carla M Abreu, Jianle Wang, Montserrat C Anguera, Dirk G de Rooij, Maria Jasin, P Jeremy Wang
Publikováno v:
PLoS Genetics, Vol 11, Iss 1, p e1004954 (2015)
Polycomb group proteins mediate transcriptional silencing in diverse developmental processes. Sex chromosomes undergo chromosome-wide transcription silencing during male meiosis. Here we report that mouse SCML2 (Sex comb on midleg-like 2), an X chrom
Externí odkaz:
https://doaj.org/article/621c5b5e66ee41edb4a88fdf68d700cc
Autor:
Montserrat C Anguera, Weiyuan Ma, Danielle Clift, Satoshi Namekawa, Raymond J Kelleher, Jeannie T Lee
Publikováno v:
PLoS Genetics, Vol 7, Iss 9, p e1002248 (2011)
The Tsx gene resides at the X-inactivation center and is thought to encode a protein expressed in testis, but its function has remained mysterious. Given its proximity to noncoding genes that regulate X-inactivation, here we characterize Tsx and dete
Externí odkaz:
https://doaj.org/article/9354dfba9175408599a070d580d120a6
Autor:
Suhee Chang, Stella K. Hur, Natali S. Sobel Naveh, Joanne L. Thorvaldsen, Deborah L. French, Alyssa L Gagne, Chintan D. Jobaliya, Montserrat C. Anguera, Marisa S. Bartolomei, Jennifer M Kalish
Publikováno v:
Epigenetics, Vol 16, Iss 12, Pp 1295-1305 (2021)
Genomic imprinting is a rare form of gene expression in mammals in which a small number of genes are expressed in a parent-of-origin-specific manner. The aetiology of human imprinting disorders is diverse and includes chromosomal abnormalities, mutat
Externí odkaz:
https://doaj.org/article/03d418f378ec4d8dbddcd0b45ec27f03
Autor:
Isabel Sierra, Sarah Pyfrom, Aaron Weiner, Gan Zhao, Amanda Driscoll, Xiang Yu, Brian D. Gregory, Andrew E. Vaughan, Montserrat C. Anguera
Publikováno v:
Stem Cell Reports. 18:489-502
Autor:
Montserrat C. Anguera
Publikováno v:
Sex, Gender, and Epigenetics ISBN: 9780128239377
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b86a83a7d488ec4c2123340103ff3640
https://doi.org/10.1016/b978-0-12-823937-7.00022-5
https://doi.org/10.1016/b978-0-12-823937-7.00022-5
Autor:
Montserrat C. Anguera, Ina Anreiter, Maria Becker, Nicolò Caporale, Stephanie Cheng, Cristina Cheroni, Stephanie Cheung, Aaron Ciechanover, Coralina Collar-Fernández, Jasmine Dennison, Sonja Entringer, Dov Feldberg, Katie A. Fennell, Anne Gabory, Donato Gemmati, Marek Glezerman, Mila Gorchkova, Denis Gorobets, Mark Green, Jane Halliday, Anthony J. Hannan, Lucas B. Hoffmann, Claudine Junien, Olena M. Kocur, Jari M. Lahti, Marianne J. Legato, Sharon Lewis, Boris Novakovic, Asher Ornoy, Susan Ozanne, Gianpiero D. Palermo, Terence Y. Pang, Zeenal H. Patel, Jacob Peedicayil, Luciana Pellegrini Pisani, Zev Rosenwaks, Richard Saffery, Daniel Sapozhnikov, Keshav K. Singh, Marla B. Sokolowski, Hermona Soreq, Sarah Stucchi, Moshe Szyf, Giuseppe Testa, Veronica Tisato, Felix Vaura, Gal Warhaftig, Liza Weinstein-Fudim, Philip Xie, Gal Yadid
Publikováno v:
Sex, Gender, and Epigenetics ISBN: 9780128239377
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e082b7eb97ec3e3f028f059386f12b4
https://doi.org/10.1016/b978-0-12-823937-7.09991-0
https://doi.org/10.1016/b978-0-12-823937-7.09991-0
Autor:
Isabel Sierra, Son C. Nguyen, R. Jordan Barnett, Ashley L. Cook, Han-Seul Ryu, Zachary T. Beethem, Jennifer E. Philips-Cremins, Eric F. Joyce, Montserrat C. Anguera
X Chromosome Inactivation (XCI) equalizes X-linked gene expression between sexes. B cells exhibit unusually dynamic XCI, as Xist RNA/heterochromatic marks on the inactive X (Xi) are absent in naïve B cells, but return following mitogenic stimulation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::338143220198a2668d21e9a3293aba1b
https://doi.org/10.1101/2022.10.19.512821
https://doi.org/10.1101/2022.10.19.512821
Autor:
Elizabeth R. Volkmann, Jill Siegfried, Tim Lahm, Corey E. Ventetuolo, Stephen C. Mathai, Virginia Steen, Erica L. Herzog, Rebecca Shansky, Montserrat C. Anguera, Sonye K. Danoff, Jon T. Giles, Yvonne C. Lee, Wonder Drake, Lisa A. Maier, Marrah Lachowicz-Scroggins, Heiyoung Park, Koyeli Banerjee, Josh Fessel, Lora Reineck, Louis Vuga, Elliott Crouser, Carol Feghali-Bostwick
Publikováno v:
American journal of respiratory and critical care medicine. 206(7)
Autor:
Deborah L. French, Joanne L. Thorvaldsen, Suhee Chang, Jennifer M. Kalish, Alyssa L. Gagne, Marisa S. Bartolomei, Montserrat C. Anguera, Stella K. Hur, Chintan D Jobaliya, Natali S Sobel Naveh
Publikováno v:
Epigenetics
Genomic imprinting is a rare form of gene expression in mammals in which a small number of genes are expressed in a parent-of-origin-specific manner. The aetiology of human imprinting disorders is diverse and includes chromosomal abnormalities, mutat