Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mohammad Sarfaraz Nawaz"'
Autor:
Natasha J. Anstey, Vijayakumar Kapgal, Shashank Tiwari, Thomas C. Watson, Anna K. H. Toft, Owen R. Dando, Felicity H. Inkpen, Paul S. Baxter, Zrinko Kozić, Adam D. Jackson, Xin He, Mohammad Sarfaraz Nawaz, Aiman Kayenaat, Aditi Bhattacharya, David J. A. Wyllie, Sumantra Chattarji, Emma R. Wood, Oliver Hardt, Peter C. Kind
Publikováno v:
Molecular Autism, Vol 13, Iss 1, Pp 1-19 (2022)
Abstract Background Mutations in the postsynaptic transmembrane protein neuroligin-3 are highly correlative with autism spectrum disorders (ASDs) and intellectual disabilities (IDs). Fear learning is well studied in models of these disorders, however
Externí odkaz:
https://doaj.org/article/3d9e90cbc8e047a6a47ce223c07a8fd8
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
There is accumulating evidence for contrasting patterns of stress-induced morphological and physiological plasticity in glutamatergic synapses of the hippocampus and amygdala. The same chronic stress that leads to the formation of dendritic spines in
Externí odkaz:
https://doaj.org/article/f8aa35c2073441d5aed2d918eb671824
Autor:
Mohammad Sarfaraz Nawaz, Elisa Giarda, Francesco Bedogni, Paolo La Montanara, Sara Ricciardi, Dalila Ciceri, Tiziana Alberio, Nicoletta Landsberger, Laura Rusconi, Charlotte Kilstrup-Nielsen
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0148634 (2016)
In the last years, the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene has been associated with epileptic encephalopathies characterized by the early onset of intractable epilepsy, severe developmental delay, autistic features, and often the dev
Externí odkaz:
https://doaj.org/article/614f3e4d5c11438a970eaa86df942e29
Autor:
Natasha J. Anstey, Vijayakumar Kapgal, Shashank Tiwari, Thomas C. Watson, Anna K. H. Toft, Owen R. Dando, Felicity H. Inkpen, Paul S. Baxter, Zrinko Kozić, Adam D. Jackson, Xin He, Mohammad Sarfaraz Nawaz, Aiman Kayenaat, Aditi Bhattacharya, David J. A. Wyllie, Sumantra Chattarji, Emma R. Wood, Oliver Hardt, Peter C. Kind
Publikováno v:
Anstey, N J, Kapgal, V, Tiwari, S, Watson, T C, Toft, A K H, Dando, O R, Inkpen, F H, Baxter, P S, Kozic, Z, Jackson, A D, He, X, Nawaz, M S, Kayenaat, A, Bhattacharya, A, Wyllie, D J A, Chattarji, S, Wood, E R, Hardt, O & Kind, P C 2022, ' Imbalance of flight-freeze responses and their cellular correlates in the Nlgn3-/y rat model of autism ', Molecular Autism, vol. 13, 34 . https://doi.org/10.1186/s13229-022-00511-8
BackgroundMutations in the postsynaptic transmembrane protein neuroligin-3 are highly correlative with autism spectrum disorders (ASDs) and intellectual disabilities (IDs). Fear learning is well studied in models of these disorders, however differenc
Autor:
Natasha J, Anstey, Vijayakumar, Kapgal, Shashank, Tiwari, Thomas C, Watson, Anna K H, Toft, Owen R, Dando, Felicity H, Inkpen, Paul S, Baxter, Zrinko, Kozić, Adam D, Jackson, Xin, He, Mohammad Sarfaraz, Nawaz, Aiman, Kayenaat, Aditi, Bhattacharya, David J A, Wyllie, Sumantra, Chattarji, Emma R, Wood, Oliver, Hardt, Peter C, Kind
Publikováno v:
Molecular autism. 13(1)
Mutations in the postsynaptic transmembrane protein neuroligin-3 are highly correlative with autism spectrum disorders (ASDs) and intellectual disabilities (IDs). Fear learning is well studied in models of these disorders, however differences in fear
Autor:
David J. A. Wyllie, Sonal Kedia, Paul G. Donlin-Asp, Sumantra Chattarji, Pradeep K. Mishra, Mohammad Sarfaraz Nawaz, Erin M. Schuman, Peter C. Kind, Giselle Fernandes, Mohammed Mostafizur Rahman, Aiman Kayenaat, Anupam Hazra, Dheeraj Songara
Publikováno v:
Cell Rep.
Fragile X syndrome (FXS), a commonly inherited form of autism and intellectual disability, is associated with emotional symptoms that implicate dysfunction of the amygdala. However, current understanding of the pathogenesis of the disease is based pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e799bbf7a8522e4560eeecf528af8083
Autor:
David J. A. Wyllie, Sumantra Chattarji, Thomas C Watson, Zrinko Kozic, Natasha J. Anstey, Adam D. Jackson, Emma R. Wood, Xin He, Shashank Tiwari, Aiman Kayenaat, Peter C. Kind, Owen Dando, Aditi Bhattacharya, Oliver Hardt, Mohammad Sarfaraz Nawaz, Anna Kh Toft, Felicity H Inkpen, Vijayakumar Kapgal, Paul Baxter
SummaryMutations in the postsynaptic transmembrane protein neuroligin-3 are highly correlative with autism spectrum disorders (ASDs) and intellectual disabilities (IDs). Fear learning is well studied in models of these disorders, however differences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c27a22c8c7a06ee869fde6d839c64ba3
https://doi.org/10.1101/2020.08.27.267880
https://doi.org/10.1101/2020.08.27.267880
Autor:
Nicoletta Landsberger, Anna Bergo, Elisa Bellini, Mohammad Sarfaraz Nawaz, Maria Maddalena Valente, Laura Rusconi, Chetan Chandola, Giulio Pavesi, Gilda Stefanelli, Charlotte Kilstrup-Nielsen, Marta Strollo, Isabella Barbiero
Publikováno v:
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience, Vol 8 (2014)
Frontiers in Cellular Neuroscience, Vol 8 (2014)
Although Rett syndrome (RTT) represents one of the most frequent forms of severe intellectual disability in females worldwide, we still have an inadequate knowledge of the many roles played by MeCP2 (whose mutations are responsible for most cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b41793e2a2da3723e7e182fb8ce4fa8
http://hdl.handle.net/11383/2019402
http://hdl.handle.net/11383/2019402
Autor:
Nicoletta Landsberger, Dalila Ciceri, Charlotte Kilstrup-Nielsen, Laura Rusconi, Mohammad Sarfaraz Nawaz, Paolo La Montanara, Tiziana Alberio, Francesco Bedogni, Elisa Giarda, Sara Ricciardi
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0148634 (2016)
PLoS ONE
PLoS ONE
In the last years, the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene has been associated with epileptic encephalopathies characterized by the early onset of intractable epilepsy, severe developmental delay, autistic features, and often the dev