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Proteome Science
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February 3, 2017
Overgrazing induces alterations in the hepatic proteome of sheep (<i>Ovis aries</i>): an iTRAQ-based quantitative proteomic analysis
Weibo Ren, Xiangyang Hou, Yuqing Wang, et al.
Brain : a Journal of Neurology
|
August 23, 2019
Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromes
Yi-Wu Shi, Qi Zhang, Kefu Cai, et al.
Brain : a Journal of Neurology
|
May 7, 2019
Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies
Ciria C Hernandez, Wenshu XiangWei, Ningning Hu, et al.
Epilepsy & Behavior : E&B
|
September 11, 2022
Repeated long sessions of transcranial direct current stimulation reduces seizure frequency in patients with refractory focal epilepsy: An open-label extension study
Dongju Yang, Rui Ma, Nuo Yang, et al.
Biomaterials Science
|
May 14, 2026
Inhalable viromimetic polymer nanoparticle vaccine (iVPNVax) in a subcutaneous-prime/inhalation-boost vaccination schedule for eliciting durable mucosal and systemic immune protection
Zhenyi Zhu, Xinyu Zhuang, Zichao Huang, et al.
Brain : a Journal of Neurology
|
November 20, 2016
De novo GABRG2 mutations associated with epileptic encephalopathies
Dingding Shen, Ciria C Hernandez, Wangzhen Shen, et al.
Blood Advances
|
March 20, 2024
Multiomic profiling of human clonal hematopoiesis reveals genotype and cell-specific inflammatory pathway activation
J Brett Heimlich, Pawan Bhat, Alyssa C Parker, et al.
HGG Advances
|
August 29, 2022
Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by <i>de novo</i> KCNC2 variants
Souhrid Mukherjee, Thomas A Cassini, Ningning Hu, et al.
Clinical Kidney Journal
|
October 8, 2025
Age at disease onset and risk of chronic kidney disease in patients with heterozygous disease-causing variants in <i>COL4A3</i> and <i>COL4A4</i>
Ningning Hu, Lei Sun, Xuantong Dai, et al.
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Search research articles
Search
Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Proteome Science
|
February 3, 2017
Overgrazing induces alterations in the hepatic proteome of sheep (<i>Ovis aries</i>): an iTRAQ-based quantitative proteomic analysis
Weibo Ren, Xiangyang Hou, Yuqing Wang, et al.
Brain : a Journal of Neurology
|
August 23, 2019
Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromes
Yi-Wu Shi, Qi Zhang, Kefu Cai, et al.
Brain : a Journal of Neurology
|
May 7, 2019
Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies
Ciria C Hernandez, Wenshu XiangWei, Ningning Hu, et al.
Epilepsy & Behavior : E&B
|
September 11, 2022
Repeated long sessions of transcranial direct current stimulation reduces seizure frequency in patients with refractory focal epilepsy: An open-label extension study
Dongju Yang, Rui Ma, Nuo Yang, et al.
Biomaterials Science
|
May 14, 2026
Inhalable viromimetic polymer nanoparticle vaccine (iVPNVax) in a subcutaneous-prime/inhalation-boost vaccination schedule for eliciting durable mucosal and systemic immune protection
Zhenyi Zhu, Xinyu Zhuang, Zichao Huang, et al.
Brain : a Journal of Neurology
|
November 20, 2016
De novo GABRG2 mutations associated with epileptic encephalopathies
Dingding Shen, Ciria C Hernandez, Wangzhen Shen, et al.
Blood Advances
|
March 20, 2024
Multiomic profiling of human clonal hematopoiesis reveals genotype and cell-specific inflammatory pathway activation
J Brett Heimlich, Pawan Bhat, Alyssa C Parker, et al.
HGG Advances
|
August 29, 2022
Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by <i>de novo</i> KCNC2 variants
Souhrid Mukherjee, Thomas A Cassini, Ningning Hu, et al.
Clinical Kidney Journal
|
October 8, 2025
Age at disease onset and risk of chronic kidney disease in patients with heterozygous disease-causing variants in <i>COL4A3</i> and <i>COL4A4</i>
Ningning Hu, Lei Sun, Xuantong Dai, et al.
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