Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Zeeba D. Kabir"'
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
Autor:
Andrew A. Pieper, Emiko Miller, Edwin Vázquez-Rosa, Alexander P. Walsh, Coral J. Cintrón-Pérez, Jonathan E. Hackett, Herie Sun, Anjali M. Rajadhyaksha, Yeojung Koh, Charlotte C. Bavley, Maria Kosovsky, Zeeba D. Kabir
Publikováno v:
Mol Psychiatry
Post-traumatic stress disorder (PTSD) is characterized by persistent fear memory of remote traumatic events, mental re-experiencing of the trauma, long-term cognitive deficits, and PTSD-associated hippocampal dysfunction. Extinction-based therapeutic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3af405643344edc7fd8f37dfdb93fc51
https://doi.org/10.1038/s41380-020-0730-8
https://doi.org/10.1038/s41380-020-0730-8
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e84165 (2013)
Prenatal cocaine exposure has been shown to alter cognitive processes of exposed individuals, presumed to be a result of long-lasting molecular alterations in the brain. In adult prenatal cocaine exposed (PCOC) mice we have identified a deficit in re
Externí odkaz:
https://doaj.org/article/ef6015cbb4c548f19ed38f55c6ef2dc3
Autor:
Delaney K. Fischer, Anjali M. Rajadhyaksha, Bryant K. Rizzo, Zeeba D. Kabir, N V De Marco Garcia, Alicia Che, Richard C. Rice, Michael J. Glass, M Byrne
Publikováno v:
Molecular Psychiatry. 22:1096-1109
CACNA1C, encoding the Cav1.2 subunit of L-type Ca2+ channels, has emerged as one of the most prominent and highly replicable susceptibility genes for several neuropsychiatric disorders. Cav1.2 channels play a crucial role in calcium-mediated processe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f3b3881355b9fd55f10047eac44e58c
https://doi.org/10.1038/mp.2017.124
https://doi.org/10.1038/mp.2017.124
Autor:
Josephine L. Belluardo, Alana I. Mendelsohn, Peter van Roessel, Julia A. Kaltschmidt, Joseph P. Pierce, George Z. Mentis, Anna Francesconi, Zeeba D. Kabir, Robert H. Edwards, Kathryn C. Schierberl, Praveen K. Bommareddy, Teresa A. Milner, Anjali M. Rajadhyaksha, Jarret A.P. Weinrich, John G. Pagiazitis, Michael Mende, Emily V. Fletcher
Publikováno v:
Neuron
Circuit function in the CNS relies on the balanced interplay of excitatory and inhibitory synaptic signaling. How neuronal activity influences synaptic differentiation to maintain such balance remains unclear. In the mouse spinal cord, a population o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c37e2506589010a2ae0ddf867b0281a
https://doi.org/10.1016/j.neuron.2016.05.008
https://doi.org/10.1016/j.neuron.2016.05.008
Publikováno v:
The Journal of Physiology. 594:5823-5837
Brain Cav 1.2 and Cav 1.3 L-type Ca2+ channels play key physiological roles in various neuronal processes that contribute to brain function. Genetic studies have recently identified CACNA1C as a candidate risk gene for bipolar disorder (BD), schizoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ce241897a9932d6ea8d9fdf0d2e1fae
https://doi.org/10.1113/jp270673
https://doi.org/10.1113/jp270673
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:
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics. 14(3)
The L-type calcium channels (LTCCs) Cav1.2 and Cav1.3, encoded by the CACNA1C and CACNA1D genes, respectively, are important regulators of calcium influx into cells and are critical for normal brain development and plasticity. In humans, CACNA1C has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb601be0037bbed563f811eeb7c9f753
https://pubmed.ncbi.nlm.nih.gov/28497380
https://pubmed.ncbi.nlm.nih.gov/28497380