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Xianlin Liu

Showing results (11-20 of 26) with videos related to

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Frontiers in Psychiatry|November 15, 2023
Impaired olfactory function in bipolar disorder patients during acute episodes regardless of psychotic symptomsYingying Li, Huiqian Yuan, Xianlin Liu, et al.
BMC Psychiatry|October 23, 2024
Association between olfactory function and metabolic syndrome in bipolar disorder patients: a cross-sectional studyHuiqian Yuan, Yingying Li, Xianlin Liu, et al.
Frontiers in Psychiatry|April 23, 2024
Significant improvements in the olfactory sensitivity of bipolar I disorder patients during euthymia versus manic episodes: a longitudinal studyXianlin Liu, Langjun Su, Yingying Li, et al.
Stem Cell Research|September 20, 2022
Establishment of two iPSC lines from healthy donor with heterozygous mutation in the SLC26A4 geneSiJun Li, Chufeng He, Qi Feng, et al.
Stem Cell Research|March 28, 2021
Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutationJie Wen, Chufeng He, Yong Feng, et al.
Human Molecular Genetics|September 1, 2022
A non-coding variant in 5' untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humansSida Huang, Lu Ma, Xuezhong Liu, et al.
Redox Biology|June 13, 2024
ABCC1 deficiency potentiated noise-induced hearing loss in mice by impairing cochlear antioxidant capacityJing Liu, Yijiang Bai, Yong Feng, et al.
Biomedicines|May 4, 2026
DYRK1B Inhibition by AZ191 Sensitizes High-Grade Serous Ovarian Cancer to Niraparib Through Promoting Apoptosis and FerroptosisYu Gao, Yuanyuan Cao, Junyao Liu, et al.
Frontiers in Molecular Neuroscience|January 21, 2025
Modeling of auditory neuropathy spectrum disorders associated with the <i>TEME43</i> variant reveals impaired gap junction function of iPSC-derived glia-like support cellsXiaoming Kang, Lu Ma, Jie Wen, et al.
Scientific Reports|July 31, 2025
Full length transcriptomic profiling reveals insights into the white coat phenotype in Waardenburg syndrome mice harboring the Mitf R324del mutationWei Gong, Lu Ma, Zhili Feng, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Frontiers in Psychiatry|November 15, 2023
Impaired olfactory function in bipolar disorder patients during acute episodes regardless of psychotic symptomsYingying Li, Huiqian Yuan, Xianlin Liu, et al.
BMC Psychiatry|October 23, 2024
Association between olfactory function and metabolic syndrome in bipolar disorder patients: a cross-sectional studyHuiqian Yuan, Yingying Li, Xianlin Liu, et al.
Frontiers in Psychiatry|April 23, 2024
Significant improvements in the olfactory sensitivity of bipolar I disorder patients during euthymia versus manic episodes: a longitudinal studyXianlin Liu, Langjun Su, Yingying Li, et al.
Stem Cell Research|September 20, 2022
Establishment of two iPSC lines from healthy donor with heterozygous mutation in the SLC26A4 geneSiJun Li, Chufeng He, Qi Feng, et al.
Stem Cell Research|March 28, 2021
Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutationJie Wen, Chufeng He, Yong Feng, et al.
Human Molecular Genetics|September 1, 2022
A non-coding variant in 5' untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humansSida Huang, Lu Ma, Xuezhong Liu, et al.
Redox Biology|June 13, 2024
ABCC1 deficiency potentiated noise-induced hearing loss in mice by impairing cochlear antioxidant capacityJing Liu, Yijiang Bai, Yong Feng, et al.
Biomedicines|May 4, 2026
DYRK1B Inhibition by AZ191 Sensitizes High-Grade Serous Ovarian Cancer to Niraparib Through Promoting Apoptosis and FerroptosisYu Gao, Yuanyuan Cao, Junyao Liu, et al.
Frontiers in Molecular Neuroscience|January 21, 2025
Modeling of auditory neuropathy spectrum disorders associated with the <i>TEME43</i> variant reveals impaired gap junction function of iPSC-derived glia-like support cellsXiaoming Kang, Lu Ma, Jie Wen, et al.
Scientific Reports|July 31, 2025
Full length transcriptomic profiling reveals insights into the white coat phenotype in Waardenburg syndrome mice harboring the Mitf R324del mutationWei Gong, Lu Ma, Zhili Feng, et al.
Pageof 3