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Chunnuan Chen

Showing results (31-40 of 64) with videos related to

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Human Mutation|May 11, 2026
Identification of Two Novel Variants in <i>CRYGD</i> and <i>OCRL</i> Genes in the Chinese Population With Hereditary Congenital Cataracts Using Whole Exome SequencingJianlong Zhuang, Nan Huang, Yu E Chen, et al.
Journal of Neuroinflammation|April 22, 2018
Omega-3 polyunsaturated fatty acid attenuates the inflammatory response by modulating microglia polarization through SIRT1-mediated deacetylation of the HMGB1/NF-κB pathway following experimental traumatic brain injuryXiangrong Chen, Chunnuan Chen, Sining Fan, et al.
Journal of Materials Chemistry. B|June 9, 2025
Nanozymes in Parkinson's disease: strategic approaches, clinical considerations, and challengesWanli Huang, Xiaofang Ye, Zhengping Huang, et al.
Molecular Cytogenetics|June 7, 2022
Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese populationJianlong Zhuang, Chunnuan Chen, Rongfu Huang, et al.
International Immunopharmacology|April 16, 2026
Targeting HIF-1α rescues microglial efferocytosis via the SLC7A11-TAM pathway to ameliorate Sepsis-associated encephalopathyShengnan Wang, Youfang Chen, Zhendong Sun, et al.
BMC Pregnancy and Childbirth|January 29, 2021
Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, ChinaJianlong Zhuang, Chunnuan Chen, Yuying Jiang, et al.
Molecular Genetics & Genomic Medicine|July 24, 2023
Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndromeJianlong Zhuang, Shufen Liu, Junyu Wang, et al.
Frontiers in Genetics|July 22, 2022
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the <i>KCNH2</i> Gene in a Fetus With Familial 2q14.2 DuplicationJianlong Zhuang, Chunnuan Chen, Yuanbai Wang, et al.
Birth Defects Research|August 27, 2024
Whole Exome Sequencing Revealing a Novel PBX1 Gene Variant in a Chinese Family Causing Recurrent Neonatal DeathNan Huang, Hegan Zhang, Zhengping Huang, et al.
Molecular Genetics & Genomic Medicine|December 12, 2022
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature reviewJianlong Zhuang, Qi Luo, Meihua Xie, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Human Mutation|May 11, 2026
Identification of Two Novel Variants in <i>CRYGD</i> and <i>OCRL</i> Genes in the Chinese Population With Hereditary Congenital Cataracts Using Whole Exome SequencingJianlong Zhuang, Nan Huang, Yu E Chen, et al.
Journal of Neuroinflammation|April 22, 2018
Omega-3 polyunsaturated fatty acid attenuates the inflammatory response by modulating microglia polarization through SIRT1-mediated deacetylation of the HMGB1/NF-κB pathway following experimental traumatic brain injuryXiangrong Chen, Chunnuan Chen, Sining Fan, et al.
Journal of Materials Chemistry. B|June 9, 2025
Nanozymes in Parkinson's disease: strategic approaches, clinical considerations, and challengesWanli Huang, Xiaofang Ye, Zhengping Huang, et al.
Molecular Cytogenetics|June 7, 2022
Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese populationJianlong Zhuang, Chunnuan Chen, Rongfu Huang, et al.
International Immunopharmacology|April 16, 2026
Targeting HIF-1α rescues microglial efferocytosis via the SLC7A11-TAM pathway to ameliorate Sepsis-associated encephalopathyShengnan Wang, Youfang Chen, Zhendong Sun, et al.
BMC Pregnancy and Childbirth|January 29, 2021
Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, ChinaJianlong Zhuang, Chunnuan Chen, Yuying Jiang, et al.
Molecular Genetics & Genomic Medicine|July 24, 2023
Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndromeJianlong Zhuang, Shufen Liu, Junyu Wang, et al.
Frontiers in Genetics|July 22, 2022
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the <i>KCNH2</i> Gene in a Fetus With Familial 2q14.2 DuplicationJianlong Zhuang, Chunnuan Chen, Yuanbai Wang, et al.
Birth Defects Research|August 27, 2024
Whole Exome Sequencing Revealing a Novel PBX1 Gene Variant in a Chinese Family Causing Recurrent Neonatal DeathNan Huang, Hegan Zhang, Zhengping Huang, et al.
Molecular Genetics & Genomic Medicine|December 12, 2022
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole-exome sequencing: A rare case report and literature reviewJianlong Zhuang, Qi Luo, Meihua Xie, et al.
Pageof 7