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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 28, 2012
The intronic GABRG2 mutation, IVS6+2T->G, associated with childhood absence epilepsy altered subunit mRNA intron splicing, activated nonsense-mediated decay, and produced a stable truncated γ2 subunit
Mengnan Tian, Robert L Macdonald
Mathematical Biosciences and Engineering : MBE
|
November 3, 2023
A double association-based evolutionary algorithm for many-objective optimization
Junhua Liu, Wei Zhang, Mengnan Tian, et al.
Optics Express
|
October 14, 2022
Investigation on the pulse response of a spin-exchange relaxation-free comagnetometer
Jiali Liu, Liwei Jiang, Yixiang Liang, et al.
Neurobiology of Disease
|
July 4, 2012
The GABRG2 nonsense mutation, Q40X, associated with Dravet syndrome activated NMD and generated a truncated subunit that was partially rescued by aminoglycoside-induced stop codon read-through
Xuan Huang, Mengnan Tian, Ciria C Hernandez, et al.
Channels (Austin, Tex.)
|
February 26, 2020
PAC proton-activated chloride channel contributes to acid-induced cell death in primary rat cortical neurons
James Osei-Owusu, Junhua Yang, Maria Del Carmen Vitery, et al.
Optics Letters
|
June 1, 2023
Single-beam NMOR atomic magnetometer based on a fiberized EOM
Mengnan Tian, Wei Quan, Liwei Jiang, et al.
Optics Express
|
July 30, 2025
Refined analysis and representation of atomic polarization in NMOR atomic magnetometers
Yanchao Chai, Liwei Jiang, Jiali Liu, et al.
Neurobiology of Disease
|
October 17, 2012
Impaired surface αβγ GABA(A) receptor expression in familial epilepsy due to a GABRG2 frameshift mutation
Mengnan Tian, Davide Mei, Elena Freri, et al.
Epilepsia
|
June 7, 2017
Overexpressing wild-type γ2 subunits rescued the seizure phenotype in Gabrg2<sup>+/Q390X</sup> Dravet syndrome mice
Xuan Huang, Chengwen Zhou, Mengnan Tian, et al.
Neuron
|
November 15, 2022
The miR-124-AMPAR pathway connects polygenic risks with behavioral changes shared between schizophrenia and bipolar disorder
Ho Namkung, Hiroshi Yukitake, Daisuke Fukudome, et al.
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Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 28, 2012
The intronic GABRG2 mutation, IVS6+2T->G, associated with childhood absence epilepsy altered subunit mRNA intron splicing, activated nonsense-mediated decay, and produced a stable truncated γ2 subunit
Mengnan Tian, Robert L Macdonald
Mathematical Biosciences and Engineering : MBE
|
November 3, 2023
A double association-based evolutionary algorithm for many-objective optimization
Junhua Liu, Wei Zhang, Mengnan Tian, et al.
Optics Express
|
October 14, 2022
Investigation on the pulse response of a spin-exchange relaxation-free comagnetometer
Jiali Liu, Liwei Jiang, Yixiang Liang, et al.
Neurobiology of Disease
|
July 4, 2012
The GABRG2 nonsense mutation, Q40X, associated with Dravet syndrome activated NMD and generated a truncated subunit that was partially rescued by aminoglycoside-induced stop codon read-through
Xuan Huang, Mengnan Tian, Ciria C Hernandez, et al.
Channels (Austin, Tex.)
|
February 26, 2020
PAC proton-activated chloride channel contributes to acid-induced cell death in primary rat cortical neurons
James Osei-Owusu, Junhua Yang, Maria Del Carmen Vitery, et al.
Optics Letters
|
June 1, 2023
Single-beam NMOR atomic magnetometer based on a fiberized EOM
Mengnan Tian, Wei Quan, Liwei Jiang, et al.
Optics Express
|
July 30, 2025
Refined analysis and representation of atomic polarization in NMOR atomic magnetometers
Yanchao Chai, Liwei Jiang, Jiali Liu, et al.
Neurobiology of Disease
|
October 17, 2012
Impaired surface αβγ GABA(A) receptor expression in familial epilepsy due to a GABRG2 frameshift mutation
Mengnan Tian, Davide Mei, Elena Freri, et al.
Epilepsia
|
June 7, 2017
Overexpressing wild-type γ2 subunits rescued the seizure phenotype in Gabrg2<sup>+/Q390X</sup> Dravet syndrome mice
Xuan Huang, Chengwen Zhou, Mengnan Tian, et al.
Neuron
|
November 15, 2022
The miR-124-AMPAR pathway connects polygenic risks with behavioral changes shared between schizophrenia and bipolar disorder
Ho Namkung, Hiroshi Yukitake, Daisuke Fukudome, et al.
Page
of 1