Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ana Petracovici"'
Autor:
Marco Trizzino, Elisa Barbieri, Ana Petracovici, Shuai Wu, Sarah A. Welsh, Tori A. Owens, Silvia Licciulli, Rugang Zhang, Alessandro Gardini
Publikováno v:
Cell Reports, Vol 23, Iss 13, Pp 3933-3945 (2018)
Summary: AT-rich interactive domain-containing proteins 1A and 1B (ARID1A and ARID1B) are mutually exclusive subunits of the chromatin remodeler SWI/SNF. ARID1A is the most frequently mutated chromatin regulator across all cancers, and ovarian clear
Externí odkaz:
https://doaj.org/article/aab9c38312a740ed8d32bc849ec677da
Autor:
Mahdieh Jadaliha, Omid Gholamalamdari, Wei Tang, Yang Zhang, Ana Petracovici, Qinyu Hao, Aamira Tariq, Tae Gyoon Kim, Sarah E Holton, Deepak K Singh, Xiao Ling Li, Susan M Freier, Stefan Ambs, Rohit Bhargava, Ashish Lal, Supriya G Prasanth, Jian Ma, Kannanganattu V Prasanth
Publikováno v:
PLoS Genetics, Vol 14, Iss 11, p e1007802 (2018)
The human genome encodes thousands of long noncoding RNA (lncRNA) genes; the function of majority of them is poorly understood. Aberrant expression of a significant number of lncRNAs is observed in various diseases, including cancer. To gain insights
Externí odkaz:
https://doaj.org/article/a0328846c8c04517aa1e82a87eb95ca4
Autor:
Ana Petracovici, Roberto Bonasio
Publikováno v:
Mol Cell
The Polycomb repressive complex 2 (PRC2) is an essential epigenetic regulator that deposits repressive H3K27me3. PRC2 subunits form two holocomplexes-PRC2.1 and PRC2.2-but the roles of these two PRC2 assemblies during differentiation are unclear. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaa34ee5c42add67a2e12620422a67da
https://europepmc.org/articles/PMC8217195/
https://europepmc.org/articles/PMC8217195/
Autor:
Eleanor G. Seaby, Marwan Shinawi, Raymond J. Louie, Aida Telegrafi, Suzanne M. Leal, Julien Buratti, Ana Petracovici, David B. Beck, Muhammad Arif Nadeem Saqib, Boris Keren, Sivagamy Sithambaram, Muhammad Zahid, Marie-Christine Nougues, Sander Pajusalu, Jill A. Fahrner, Eloise J. Prijoles, G. Bradley Schaefer, Dustin Baldridge, Trudie Cottrell, Regie Lyn P. Santos-Cortez, Roberto Bonasio, Tiia Reimand, Muhammad Ansar, Kirsty McWalter, Sofia Douzgou, Cyril Mignot, Siddharth Banka, Hannah W. Moore, Chongsheng He, Roger E. Stevenson, Katrin Õunap, Renee Bend
Germline pathogenic variants in chromatin-modifying enzymes are a common cause of pediatric developmental disorders. These enzymes catalyze reactions that regulate epigenetic inheritance via histone post-translational modifications and DNA methylatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b252a93b681045e4e6abb069876ac02
Autor:
Tiia Reimand, Kirsty McWalter, Eleanor G. Seaby, G. Bradley Schaefer, Marwan Shinawi, Muhammad Arif Nadeem Saqib, Aida Telegrafi, Ana Petracovici, Sander Pajusalu, Jill A. Fahrner, David B. Beck, Chongsheng He, Hannah W. Moore, Suzanne M. Leal, Raymond J. Louie, Siddharth Banka, Renee Bend, Regie Lyn P. Santos-Cortez, Roberto Bonasio, Boris Keren, Marie Christine Nougues, Eloise J. Prijoles, Muhammad Ansar, Katrin Õunap, Roger E. Stevenson, Julien Buratti, Sofia Douzgou, Cyril Mignot, Sivagamy Sithambaram, Trudie Cottrell, Dustin Baldridge, Muhammad Zahid
Publikováno v:
Am J Hum Genet
Beck, D B, Petracovici, A, He, C, Moore, H W, Louie, R J, Ansar, M, Douzgou, S, Sithambaram, S, Cottrell, T, Santos-Cortez, R L P, Prijoles, E J, Bend, R, Keren, B, Mignot, C, Nougues, M-C, Õunap, K, Reimand, T, Pajusalu, S, Saqib, M A N, Buratti, J, Seaby, E G, McWalter, K, Telegrafi, A, Baldridge, D, Shinawi, M, Leal, S M, Schaefer, G B, Stevenson, R E, Banka, S, Bonasio, R & Fahrner, J A 2020, ' Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery : TET3 Deficiency ', American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2019.12.007
Beck, D B, Petracovici, A, He, C, Moore, H W, Louie, R J, Ansar, M, Douzgou, S, Sithambaram, S, Cottrell, T, Santos-Cortez, R L P, Prijoles, E J, Bend, R, Keren, B, Mignot, C, Nougues, M-C, Õunap, K, Reimand, T, Pajusalu, S, Saqib, M A N, Buratti, J, Seaby, E G, McWalter, K, Telegrafi, A, Baldridge, D, Shinawi, M, Leal, S M, Schaefer, G B, Stevenson, R E, Banka, S, Bonasio, R & Fahrner, J A 2020, ' Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery : TET3 Deficiency ', American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2019.12.007
Germline pathogenic variants in chromatin-modifying enzymes are a common cause of pediatric developmental disorders. These enzymes catalyze reactions that regulate epigenetic inheritance via histone post-translational modifications and DNA methylatio
Long noncoding RNAs (lncRNAs) are transcripts that do not code for proteins, but nevertheless exert regulatory effects on various biochemical pathways, in part via interactions with proteins, DNA, and other RNAs. LncRNAs are thought to regulate trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::441d9c3568d197cd0efd8624d44f7b64
https://europepmc.org/articles/PMC6745715/
https://europepmc.org/articles/PMC6745715/
Autor:
Elisa Barbieri, Sarah A. Welsh, Shuai Wu, Ana Petracovici, Rugang Zhang, Silvia Licciulli, Alessandro Gardini, Tori A. Owens, Marco Trizzino
Publikováno v:
Cell Reports, Vol 23, Iss 13, Pp 3933-3945 (2018)
Summary: AT-rich interactive domain-containing proteins 1A and 1B (ARID1A and ARID1B) are mutually exclusive subunits of the chromatin remodeler SWI/SNF. ARID1A is the most frequently mutated chromatin regulator across all cancers, and ovarian clear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::351eb332f8785d7bdfe60c85df3612c2
https://europepmc.org/articles/PMC6146183/
https://europepmc.org/articles/PMC6146183/
Autor:
Aamira Tariq, Yang Zhang, Ashish Lal, Tae Gyoon Kim, Jian Ma, Supriya G. Prasanth, Kannanganattu V. Prasanth, Ana Petracovici, Susan M. Freier, Qinyu Hao, Wei Tang, Rohit Bhargava, Sarah E. Holton, Omid Gholamalamdari, Xiaoling Li, Mahdieh Jadaliha, Stefan Ambs, Deepak Singh
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 14, Iss 11, p e1007802 (2018)
PLoS Genetics, Vol 14, Iss 11, p e1007802 (2018)
The human genome encodes thousands of long noncoding RNA (lncRNA) genes; the function of majority of them is poorly understood. Aberrant expression of a significant number of lncRNAs is observed in various diseases, including cancer. To gain insights