Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Yasemin Onder"'
Autor:
Yasemin Onder, Isara Laothamatas, Stefano Berto, Katharina Sewart, Gokhul Kilaru, Bogdan Bordieanu, Jeremy J. Stubblefield, Genevieve Konopka, Prashant Mishra, Carla B. Green
Publikováno v:
iScience, Vol 19, Iss , Pp 83-92 (2019)
Summary: Fine-tuning of transcriptional responses can be critical for long-term outcomes in response to an environmental challenge. The circadian protein Nocturnin belongs to a family of proteins that include exonucleases, endonucleases, and phosphat
Externí odkaz:
https://doaj.org/article/9ad9f6c4ab354745b2182dc538214cf9
Autor:
Yasemin Onder, Carla B. Green
Publikováno v:
Neurobiology of Sleep and Circadian Rhythms, Vol 4, Iss , Pp 57-63 (2018)
Circadian clocks synchronize the daily functions of organisms with environmental cues like light-dark cycles and feeding rhythms. The master clock in the suprachiasmatic nucleus in the hypothalamus of the brain and the many clocks in the periphery ar
Externí odkaz:
https://doaj.org/article/666e530cd3a04419b016f8e6f02df4ee
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:
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
Publikováno v:
Educational Assessment, Evaluation and Accountability.
Publikováno v:
Journal of Psychoeducational Assessment. 40:482-498
Teacher data-driven decision making (DDDM) is a professional practice of great prominence in the current K-12 education system. Moreover, teacher self-efficacy and anxiety around DDDM represent important measurement targets in both research and pract
Autor:
Carla B. Green, Yasemin Onder, Gokhul Kilaru, Isara Laothamatas, Prashant Mishra, Jeremy J. Stubblefield, Genevieve Konopka, Katharina Sewart, Bogdan Bordieanu, Stefano Berto
Publikováno v:
iScience
iScience, Vol 19, Iss, Pp 83-92 (2019)
iScience, Vol 19, Iss, Pp 83-92 (2019)
Summary Fine-tuning of transcriptional responses can be critical for long-term outcomes in response to an environmental challenge. The circadian protein Nocturnin belongs to a family of proteins that include exonucleases, endonucleases, and phosphata
Publikováno v:
Teaching and Teacher Education. 109:103546
Teacher induction is regarded as an important facet of the teacher education system in many countries. However, important questions remain concerning which teacher induction practices are most associated with teacher quality and retention. This study
Autor:
Yasemin Onder, Carla B. Green
Publikováno v:
Neurobiology of sleep and circadian rhythms
Neurobiology of Sleep and Circadian Rhythms, Vol 4, Iss, Pp 57-63 (2018)
Neurobiology of Sleep and Circadian Rhythms, Vol 4, Iss, Pp 57-63 (2018)
Circadian clocks synchronize the daily functions of organisms with environmental cues like light-dark cycles and feeding rhythms. The master clock in the suprachiasmatic nucleus in the hypothalamus of the brain and the many clocks in the periphery ar
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