Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Madelen M. Díaz"'
Publikováno v:
Cell Death & Differentiation. 30:397-406
Hallmark pathological features of brain trauma are axonal degeneration and demyelination because myelin-producing oligodendrocytes (OLs) are particularly vulnerable to injury-induced death signals. To reveal mechanisms responsible for this OL loss, w
Neuron-specific knockouts indicate the importance of network communication to Drosophila rhythmicity
Publikováno v:
eLife, Vol 8 (2019)
Animal circadian rhythms persist in constant darkness and are driven by intracellular transcription-translation feedback loops. Although these cellular oscillators communicate, isolated mammalian cellular clocks continue to tick away in darkness with
Externí odkaz:
https://doaj.org/article/a7ff6fa3445b4ed1b1d536be98cf21f4
Autor:
Stephen A. Tapanes, Dena Arizanovska, Madelen M. Díaz, Oluwarotimi O. Folorunso, Theresa Harvey, Stephanie E. Brown, Inna Radzishevsky, Liesl N. Close, Jonathan R. Jagid, Joacir Graciolli Cordeiro, Herman Wolosker, Darrick T. Balu, Daniel J. Liebl
Publikováno v:
Glia. 70:1133-1152
Synaptic damage is one of the most prevalent pathophysiological responses to traumatic CNS injury and underlies much of the associated cognitive dysfunction; however, it is poorly understood. The D-amino acid, D-serine, serves as the primary co-agoni
Autor:
Coleen M. Atkins, Madelen M Díaz, Yanina Tsenkina, Stephen A. Tapanes, Ross Bullock, Daniel J. Liebl, David J. Titus, Shyam Gajavelli
Publikováno v:
Brain Communications
Clinical trials examining neuroprotective strategies after brain injury, including those targeting cell death mechanisms, have been underwhelming. This may be in part due to an incomplete understanding of the signalling mechanisms that induce cell de
Neuron-specific knockouts indicate the importance of network communication to Drosophila rhythmicity
Publikováno v:
eLife
eLife, Vol 8 (2019)
eLife, Vol 8 (2019)
Animal circadian rhythms persist in constant darkness and are driven by intracellular transcription-translation feedback loops. Although these cellular oscillators communicate, isolated mammalian cellular clocks continue to tick away in darkness with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9794d0217265076ae086d77ea17e5ec7
Six neuropeptides are expressed within the Drosophila brain circadian network. Our previous mRNA profiling suggested that AllatostatinC is a seventh neuropeptide and specifically expressed in dorsal clock neurons (DN1s). Our results here show that As
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03fb73ed013fc00ff71859c48d0c017a
https://doi.org/10.1101/361048
https://doi.org/10.1101/361048
Autor:
Patrick Weidner, Pamela Menegazzi, Madelen M. Díaz, Michael Rosbash, Elena Dalla Benetta, Matthias Schlichting, Charlotte Helfrich-Förster
Publikováno v:
Current Biology. 29:3266-3276.e3
Summary The circadian clock is a timekeeper but also helps adapt physiology to the outside world. This is because an essential feature of clocks is their ability to adjust (entrain) to the environment, with light being the most important signal. Wher
Publikováno v:
Current Biology. 29:13-22.e3
Summary Seven neuropeptides are expressed within the Drosophila brain circadian network. Our previous mRNA profiling suggested that Allatostatin-C (AstC) is an eighth neuropeptide and specifically expressed in dorsal clock neurons (DN1s). Our results
Publikováno v:
Neuron. 100:624-635.e4
The Drosophila core circadian circuit contains distinct groups of interacting neurons that give rise to diurnal sleep-wake patterns. Previous work showed that a subset of dorsal neurons 1 (DN1s) are sleep-promoting through their inhibition of activit
Autor:
Aoife McMahon, Hua Jin, Madelen M. Díaz, Michael Rosbash, Eranthie Weerapana, Allegra Fieldsend, Shalise M. Couvertier, Fang Guo, Weifei Luo
Publikováno v:
Neuron. 99:768-780.e3
Drosophila NonA and its mammalian ortholog NONO are members of the Drosophila behavior and human splicing (DBHS) family. NONO also has a strong circadian connection: it associates with the circadian repressor protein PERIOD (PER) and contributes to c