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Molecular Psychiatry
|
May 4, 2026
ASD mutations in the ciliary gene CEP41 impact development of projection neurons and interneurons in a human cortical organoid model
Kerstin Hasenpusch-Theil, Alexandra Lesayova, Zrinko Kozić, et al.
Cell Death & Disease
|
February 27, 2021
Targeted de-repression of neuronal Nrf2 inhibits α-synuclein accumulation
Paul S Baxter, Nóra M Márkus, Owen Dando, et al.
Plos One
|
June 18, 2016
Characterisation of CDKL5 Transcript Isoforms in Human and Mouse
Ralph D Hector, Owen Dando, Nicoletta Landsberger, et al.
Plos One
|
February 2, 2016
Expression of mRNA Encoding Mcu and Other Mitochondrial Calcium Regulatory Genes Depends on Cell Type, Neuronal Subtype, and Ca2+ Signaling
Nóra M Márkus, Philip Hasel, Jing Qiu, et al.
The Journal of Physiology
|
August 31, 2014
Ionotropic GABA and glycine receptor subunit composition in human pluripotent stem cell-derived excitatory cortical neurones
Owain T James, Matthew R Livesey, Jing Qiu, et al.
BMC Neuroscience
|
January 19, 2023
Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion
Yifei Yang, Sam A Booker, James M Clegg, et al.
Stem Cell Research
|
October 23, 2020
Generation of pure monocultures of human microglia-like cells from induced pluripotent stem cells
Poulomi Banerjee, Evdokia Paza, Emma M Perkins, et al.
Neuron
|
August 4, 2017
Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome
Sophie R Thomson, Sang S Seo, Stephanie A Barnes, et al.
Redox Biology
|
October 9, 2021
Non-canonical Keap1-independent activation of Nrf2 in astrocytes by mild oxidative stress
Bashayer R Al-Mubarak, Karen F S Bell, Sudhir Chowdhry, et al.
Human Molecular Genetics
|
March 12, 2020
Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of function
Faith C J Davies, Jilly E Hope, Fiona McLachlan, et al.
Page
of 5
Search research articles
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Showing results (11-20 of 42) with videos related to
Sort By:
Page
of 5
Molecular Psychiatry
|
May 4, 2026
ASD mutations in the ciliary gene CEP41 impact development of projection neurons and interneurons in a human cortical organoid model
Kerstin Hasenpusch-Theil, Alexandra Lesayova, Zrinko Kozić, et al.
Cell Death & Disease
|
February 27, 2021
Targeted de-repression of neuronal Nrf2 inhibits α-synuclein accumulation
Paul S Baxter, Nóra M Márkus, Owen Dando, et al.
Plos One
|
June 18, 2016
Characterisation of CDKL5 Transcript Isoforms in Human and Mouse
Ralph D Hector, Owen Dando, Nicoletta Landsberger, et al.
Plos One
|
February 2, 2016
Expression of mRNA Encoding Mcu and Other Mitochondrial Calcium Regulatory Genes Depends on Cell Type, Neuronal Subtype, and Ca2+ Signaling
Nóra M Márkus, Philip Hasel, Jing Qiu, et al.
The Journal of Physiology
|
August 31, 2014
Ionotropic GABA and glycine receptor subunit composition in human pluripotent stem cell-derived excitatory cortical neurones
Owain T James, Matthew R Livesey, Jing Qiu, et al.
BMC Neuroscience
|
January 19, 2023
Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion
Yifei Yang, Sam A Booker, James M Clegg, et al.
Stem Cell Research
|
October 23, 2020
Generation of pure monocultures of human microglia-like cells from induced pluripotent stem cells
Poulomi Banerjee, Evdokia Paza, Emma M Perkins, et al.
Neuron
|
August 4, 2017
Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome
Sophie R Thomson, Sang S Seo, Stephanie A Barnes, et al.
Redox Biology
|
October 9, 2021
Non-canonical Keap1-independent activation of Nrf2 in astrocytes by mild oxidative stress
Bashayer R Al-Mubarak, Karen F S Bell, Sudhir Chowdhry, et al.
Human Molecular Genetics
|
March 12, 2020
Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of function
Faith C J Davies, Jilly E Hope, Fiona McLachlan, et al.
Page
of 5