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Deng-Feng Zhang

Showing results (51-60 of 60) with videos related to

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Protein and Peptide Letters|May 11, 2023
Role of Fibrinogen in Type-2 Diabetes Mellitus with Diabetic Neuropathy and its Preliminary MechanismWei-Li Gu, Zhen-Hong Li, Si-Qin Zhang, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|August 6, 2015
CFH Variants Affect Structural and Functional Brain Changes and Genetic Risk of Alzheimer's DiseaseDeng-Feng Zhang, Jin Li, Huan Wu, et al.
Biological Psychiatry|June 8, 2023
Coexistence of Multiple Functional Variants and Genes Underlies Genetic Risk Locus 11p11.2 of Alzheimer's DiseaseMin Xu, Qianjin Liu, Rui Bi, et al.
Molecular Neurobiology|December 3, 2014
Validating GWAS-Identified Risk Loci for Alzheimer's Disease in Han Chinese PopulationsHui-Zhen Wang, Rui Bi, Qiu-Xiang Hu, et al.
Signal Transduction and Targeted Therapy|September 1, 2021
A novel missense variant in ACAA1 contributes to early-onset Alzheimer's disease, impairs lysosomal function, and facilitates amyloid-β pathology and cognitive declineRongcan Luo, Yu Fan, Jing Yang, et al.
Schizophrenia Research|December 3, 2014
Promoter variant rs2301228 on the neural cell adhesion molecule 1 gene confers risk of schizophrenia in Han ChineseWen Zhang, Mei-Sheng Xiao, Shuang Ji, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 27, 2025
Identification and Targeting of POLQ-Associated Hereditary Colorectal CancerNing Xu, Deng-Feng Zhang, Xiao-Xiao Shi, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 25, 2017
Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophreniaJinsong Tang, Yu Fan, Hong Li, et al.
Cell Reports. Medicine|September 17, 2025
ATM deficiency drives phenotypic diversity and Purkinje cell degeneration in a macaque model of ataxia-telangiectasiaKaiyu Xu, Ying Zhang, Yongxuan Chen, et al.
National Science Review|April 30, 2019
<i>Complement C7</i> is a novel risk gene for Alzheimer's disease in Han ChineseDeng-Feng Zhang, Yu Fan, Min Xu, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Protein and Peptide Letters|May 11, 2023
Role of Fibrinogen in Type-2 Diabetes Mellitus with Diabetic Neuropathy and its Preliminary MechanismWei-Li Gu, Zhen-Hong Li, Si-Qin Zhang, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|August 6, 2015
CFH Variants Affect Structural and Functional Brain Changes and Genetic Risk of Alzheimer's DiseaseDeng-Feng Zhang, Jin Li, Huan Wu, et al.
Biological Psychiatry|June 8, 2023
Coexistence of Multiple Functional Variants and Genes Underlies Genetic Risk Locus 11p11.2 of Alzheimer's DiseaseMin Xu, Qianjin Liu, Rui Bi, et al.
Molecular Neurobiology|December 3, 2014
Validating GWAS-Identified Risk Loci for Alzheimer's Disease in Han Chinese PopulationsHui-Zhen Wang, Rui Bi, Qiu-Xiang Hu, et al.
Signal Transduction and Targeted Therapy|September 1, 2021
A novel missense variant in ACAA1 contributes to early-onset Alzheimer's disease, impairs lysosomal function, and facilitates amyloid-β pathology and cognitive declineRongcan Luo, Yu Fan, Jing Yang, et al.
Schizophrenia Research|December 3, 2014
Promoter variant rs2301228 on the neural cell adhesion molecule 1 gene confers risk of schizophrenia in Han ChineseWen Zhang, Mei-Sheng Xiao, Shuang Ji, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 27, 2025
Identification and Targeting of POLQ-Associated Hereditary Colorectal CancerNing Xu, Deng-Feng Zhang, Xiao-Xiao Shi, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 25, 2017
Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophreniaJinsong Tang, Yu Fan, Hong Li, et al.
Cell Reports. Medicine|September 17, 2025
ATM deficiency drives phenotypic diversity and Purkinje cell degeneration in a macaque model of ataxia-telangiectasiaKaiyu Xu, Ying Zhang, Yongxuan Chen, et al.
National Science Review|April 30, 2019
<i>Complement C7</i> is a novel risk gene for Alzheimer's disease in Han ChineseDeng-Feng Zhang, Yu Fan, Min Xu, et al.
Pageof 6