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Scientific Reports
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July 27, 2017
Altered visual cortical processing in a mouse model of MECP2 duplication syndrome
Dinghong Zhang, Bin Yu, Jing Liu, et al.
European Journal of Medical Genetics
|
March 11, 2018
Whole-exome sequencing identifies rare compound heterozygous mutations in the MYBPC3 gene associated with severe familial hypertrophic cardiomyopathy
Nianwei Zhou, Shengmei Qin, Yili Liu, et al.
Scientific Reports
|
March 13, 2015
ERRATUM: Tet1-mediated DNA demethylation regulates neuronal cell death induced by oxidative stress
Yong-Juan Xin, Bo Yuan, Bin Yu, et al.
Neuroscience Bulletin
|
June 5, 2021
GABA Signaling Pathway-associated Gene PLCL1 Rare Variants May be Associated with Autism Spectrum Disorders
Fengyun Zheng, Guoyuan Liu, Ting Dang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 11, 2006
Calcium activation of the LMO4 transcription complex and its role in the patterning of thalamocortical connections
Amir H Kashani, Zilong Qiu, Linda Jurata, et al.
Protein & Cell
|
June 2, 2016
MiR-130a regulates neurite outgrowth and dendritic spine density by targeting MeCP2
Yunjia Zhang, Mengmeng Chen, Zilong Qiu, et al.
Science Bulletin
|
January 19, 2023
Molecular taxonomy of the primate amygdala via single-nucleus RNA sequencing analysis
Lei Zhang, Yanyong Cheng, Shihao Wu, et al.
Neural Regeneration Research
|
October 20, 2023
Mitophagy in neurodegenerative disease pathogenesis
Kan Yang, Yuqing Yan, Anni Yu, et al.
Biological Psychiatry
|
July 1, 2023
Discovery and Validation of Novel Genes in a Large Chinese Autism Spectrum Disorder Cohort
Jincheng Wang, Juehua Yu, Mengdi Wang, et al.
STAR Protocols
|
September 27, 2024
Protocol for the neonatal intracerebroventricular delivery of adeno-associated viral vectors for brain restoration of MECP2 for Rett syndrome
Kan Yang, Tianshu Li, Yixiao Geng, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 130) with videos related to
Sort By:
Page
of 13
Scientific Reports
|
July 27, 2017
Altered visual cortical processing in a mouse model of MECP2 duplication syndrome
Dinghong Zhang, Bin Yu, Jing Liu, et al.
European Journal of Medical Genetics
|
March 11, 2018
Whole-exome sequencing identifies rare compound heterozygous mutations in the MYBPC3 gene associated with severe familial hypertrophic cardiomyopathy
Nianwei Zhou, Shengmei Qin, Yili Liu, et al.
Scientific Reports
|
March 13, 2015
ERRATUM: Tet1-mediated DNA demethylation regulates neuronal cell death induced by oxidative stress
Yong-Juan Xin, Bo Yuan, Bin Yu, et al.
Neuroscience Bulletin
|
June 5, 2021
GABA Signaling Pathway-associated Gene PLCL1 Rare Variants May be Associated with Autism Spectrum Disorders
Fengyun Zheng, Guoyuan Liu, Ting Dang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 11, 2006
Calcium activation of the LMO4 transcription complex and its role in the patterning of thalamocortical connections
Amir H Kashani, Zilong Qiu, Linda Jurata, et al.
Protein & Cell
|
June 2, 2016
MiR-130a regulates neurite outgrowth and dendritic spine density by targeting MeCP2
Yunjia Zhang, Mengmeng Chen, Zilong Qiu, et al.
Science Bulletin
|
January 19, 2023
Molecular taxonomy of the primate amygdala via single-nucleus RNA sequencing analysis
Lei Zhang, Yanyong Cheng, Shihao Wu, et al.
Neural Regeneration Research
|
October 20, 2023
Mitophagy in neurodegenerative disease pathogenesis
Kan Yang, Yuqing Yan, Anni Yu, et al.
Biological Psychiatry
|
July 1, 2023
Discovery and Validation of Novel Genes in a Large Chinese Autism Spectrum Disorder Cohort
Jincheng Wang, Juehua Yu, Mengdi Wang, et al.
STAR Protocols
|
September 27, 2024
Protocol for the neonatal intracerebroventricular delivery of adeno-associated viral vectors for brain restoration of MECP2 for Rett syndrome
Kan Yang, Tianshu Li, Yixiao Geng, et al.
Page
of 13