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Xueyang Pan

Showing results (11-20 of 28) with videos related to

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Development (Cambridge, England)|February 23, 2018
Prothoracicotropic hormone modulates environmental adaptive plasticity through the control of developmental timingMaryJane Shimell, Xueyang Pan, Francisco A Martin, et al.
Molecular Oncology|April 18, 2012
Curcumin inhibits tumor proliferation induced by neutrophil elastase through the upregulation of α1-antitrypsin in lung cancerYan Xu, Jingjie Zhang, Jing Han, et al.
Oncotarget|November 19, 2016
Nordihydroguaiaretic acid impairs prostate cancer cell migration and tumor metastasis by suppressing neuropilin 1Xin Li, Shengjun Fan, Xueyang Pan, et al.
Human Molecular Genetics|October 18, 2022
The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survivalMengqi Ma, Xi Zhang, Yiming Zheng, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 8, 2011
Role of vimentin in the inhibitory effects of low-molecular-weight heparin on PC-3M cell adhesion to, and migration through, endotheliumYan Pan, Tianluo Lei, Bao Teng, et al.
Elife|December 11, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between in vivo and in vitro assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between <i>in vivo</i> and <i>in vitro</i> assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 16, 2020
Novel role of dynamin-related-protein 1 in dynamics of ER-lipid droplets in adipose tissueXin Li, Li Yang, Zhengmei Mao, et al.
American Journal of Human Genetics|March 3, 2022
Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizuresShenzhao Lu, Rebecca Hernan, Paul C Marcogliese, et al.
American Journal of Human Genetics|October 7, 2022
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movementShenzhao Lu, Mengqi Ma, Xiao Mao, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Development (Cambridge, England)|February 23, 2018
Prothoracicotropic hormone modulates environmental adaptive plasticity through the control of developmental timingMaryJane Shimell, Xueyang Pan, Francisco A Martin, et al.
Molecular Oncology|April 18, 2012
Curcumin inhibits tumor proliferation induced by neutrophil elastase through the upregulation of α1-antitrypsin in lung cancerYan Xu, Jingjie Zhang, Jing Han, et al.
Oncotarget|November 19, 2016
Nordihydroguaiaretic acid impairs prostate cancer cell migration and tumor metastasis by suppressing neuropilin 1Xin Li, Shengjun Fan, Xueyang Pan, et al.
Human Molecular Genetics|October 18, 2022
The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survivalMengqi Ma, Xi Zhang, Yiming Zheng, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 8, 2011
Role of vimentin in the inhibitory effects of low-molecular-weight heparin on PC-3M cell adhesion to, and migration through, endotheliumYan Pan, Tianluo Lei, Bao Teng, et al.
Elife|December 11, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between in vivo and in vitro assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between <i>in vivo</i> and <i>in vitro</i> assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 16, 2020
Novel role of dynamin-related-protein 1 in dynamics of ER-lipid droplets in adipose tissueXin Li, Li Yang, Zhengmei Mao, et al.
American Journal of Human Genetics|March 3, 2022
Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizuresShenzhao Lu, Rebecca Hernan, Paul C Marcogliese, et al.
American Journal of Human Genetics|October 7, 2022
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movementShenzhao Lu, Mengqi Ma, Xiao Mao, et al.
Pageof 3