Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Elisa S. Na"'
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0244793 (2020)
Enhancer redundancy has been postulated to provide a buffer for gene expression against genetic and environmental perturbations. While work in Drosophila has identified functionally overlapping enhancers, work in mammalian models has been limited. Re
Externí odkaz:
https://doaj.org/article/1d1ed4d4ea6644e780e76b6e3b09d6c2
Autor:
Elisa S Na, Héctor De Jesús-Cortés, Arlene Martinez-Rivera, Zeeba D Kabir, Jieqi Wang, Vijayashree Ramesh, Yasemin Onder, Anjali M Rajadhyaksha, Lisa M Monteggia, Andrew A Pieper
Publikováno v:
PLoS ONE, Vol 13, Iss 1, p e0192057 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0183026.].
Externí odkaz:
https://doaj.org/article/5fc1350bec8f45d1953c183935269266
Autor:
Megumi Adachi, Anita E. Autry, Ji Woon Kim, Elisa S. Na, Carl Björkholm, Ege T. Kavalali, Lisa M. Monteggia
Publikováno v:
Nature neuroscience
The rapidly acting antidepressants ketamine and scopolamine exert behavioral effects that can last from several days to more than a week in some patients. The molecular mechanisms underlying the maintenance of these antidepressant effects are unknown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16bbb53f1da73fb03d473a9d096fb11c
http://europepmc.org/articles/PMC8338784
http://europepmc.org/articles/PMC8338784
Autor:
Elisa S Na, Héctor De Jesús-Cortés, Arlene Martinez-Rivera, Zeeba D Kabir, Jieqi Wang, Vijayashree Ramesh, Yasemin Onder, Anjali M Rajadhyaksha, Lisa M Monteggia, Andrew A Pieper
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0183026 (2017)
Rett syndrome (RTT), a leading cause of intellectual disability in girls, is predominantly caused by mutations in the X-linked gene MECP2. Disruption of Mecp2 in mice recapitulates major features of RTT, including neurobehavioral abnormalities, which
Externí odkaz:
https://doaj.org/article/c82113b57f6b4e3289205c9e775b420c
Autor:
Anusha Mithani, Michael J. Morris, Elisa S. Na, Karen Ponce-Rubio, Jessica Frayre, Ruvaid Virk, Ida Wong, Priscila Frayre, Stephanie Bishop, Chelsy Mani
Publikováno v:
Behavioural Brain Research. 415:113518
Obesity is a complex disease that is the result of a number of different factors including genetic, environmental, and endocrine abnormalities. Given that monogenic forms of obesity are rare, it is important to identify other mechanisms that contribu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adde73eb96d63f4ae0061f0c5e3e38c6
https://doi.org/10.1016/j.bbr.2021.113518
https://doi.org/10.1016/j.bbr.2021.113518
Autor:
Jessica M. Adams, David P. Olson, Eva B. Yokosawa, Malcolm J. Low, Daniel D. Lam, Elisa S. Na
Publikováno v:
PLoS ONE 15:e0244793 (2020)
PLoS ONE
PLoS ONE, Vol 15, Iss 12, p e0244793 (2020)
PLoS ONE
PLoS ONE, Vol 15, Iss 12, p e0244793 (2020)
Enhancer redundancy has been postulated to provide a buffer for gene expression against genetic and environmental perturbations. While work in Drosophila has identified functionally overlapping enhancers, work in mammalian models has been limited. Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4463f41e8357f6bd338ca120607a926d
https://mediatum.ub.tum.de/doc/1609742/document.pdf
https://mediatum.ub.tum.de/doc/1609742/document.pdf
Publikováno v:
Neurobiology of Learning and Memory. 135:139-145
DNA methylation has been shown to impact certain forms of synaptic and behavioral plasticity that have been implicated in the development in psychiatric disorders. DNA methylation is catalyzed by DNA methyltransferase (DNMT) enzymes that continue to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50f7530839c20544cd9ceec1f0308bad
https://doi.org/10.1016/j.nlm.2016.08.012
https://doi.org/10.1016/j.nlm.2016.08.012
Autor:
Héctor De Jesús-Cortés, Yasemin Onder, Elisa S. Na, Andrew A. Pieper, Vijayashree Ramesh, Arlene Martinez-Rivera, Zeeba D. Kabir, Anjali M. Rajadhyaksha, Lisa M. Monteggia, Jieqi Wang
Publikováno v:
PLoS ONE
PLoS ONE, Vol 13, Iss 1, p e0192057 (2018)
PLoS ONE, Vol 13, Iss 1, p e0192057 (2018)
Rett syndrome (RTT), a leading cause of intellectual disability in girls, is predominantly caused by mutations in the X-linked gene MECP2. Disruption of Mecp2 in mice recapitulates major features of RTT, including neurobehavioral abnormalities, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30ba9b933b8d7eaea455f883f346ef0f
http://europepmc.org/articles/PMC5785006
http://europepmc.org/articles/PMC5785006
Autor:
Arlene Martinez-Rivera, Andrew A. Pieper, Héctor De Jesús-Cortés, Jieqi Wang, Lisa M. Monteggia, Anjali M. Rajadhyaksha, Elisa S. Na, Yasemin Onder, Vijayashree Ramesh, Zeeba D. Kabir
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 8, p e0183026 (2017)
PLoS ONE, Vol 12, Iss 8, p e0183026 (2017)
Rett syndrome (RTT), a leading cause of intellectual disability in girls, is predominantly caused by mutations in the X-linked gene MECP2. Disruption of Mecp2 in mice recapitulates major features of RTT, including neurobehavioral abnormalities, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::175c23374a219fd77179029ede37f950
http://europepmc.org/articles/PMC5559075
http://europepmc.org/articles/PMC5559075
Publikováno v:
Neurobiology of Learning and Memory. 115:30-37
Methylation of cytosine nucleotides is governed by DNA methyltransferases (DNMTs) that establish de novo DNA methylation patterns in early embryonic development (e.g., DNMT3a and DNMT3b) or maintain those patterns on hemimethylated DNA in dividing ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83ca4978931285b072e2ae8f621171c1
https://doi.org/10.1016/j.nlm.2014.06.005
https://doi.org/10.1016/j.nlm.2014.06.005