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Muqing Cao

Showing results (61-70 of 68) with videos related to

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Molecular Genetics & Genomic Medicine|October 19, 2019
Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndromeMinna Luo, Li Cao, Zongfu Cao, et al.
Journal of Medical Genetics|May 30, 2024
ZFYVE19 deficiency: a ciliopathy involving failure of cell division, with cell deathJing Yang, Ya-Nan Zhang, Ren-Xue Wang, et al.
Blood|February 11, 2026
Nucleoplasmic ZNF467 condensates boost hematopoietic stem cell engraftment via ICAM1-mediated mechanical reprogrammingYandan Chen, Jinghao Shen, Zaisheng Lin, et al.
Plos Biology|March 2, 2023
Ependymal polarity defects coupled with disorganized ciliary beating drive abnormal cerebrospinal fluid flow and spine curvature in zebrafishHaibo Xie, Yunsi Kang, Junjun Liu, et al.
Chemical Science|April 3, 2023
Heparan sulfate glycomimetics <i>via</i> iterative assembly of "clickable" disaccharidesCangjie Yang, Yu Deng, Yang Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2021
Correction to: Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndromeMinna Luo, Zaisheng Lin, Tian Zhu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2021
Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndromeMinna Luo, Zaisheng Lin, Tian Zhu, et al.
The Journal of Clinical Investigation|October 30, 2025
Ciliopathy-related B9 protein complex regulates ciliary axonemal microtubule post-translational modifications and initiation of ciliogenesisRuida He, Yan Li, Minjun Jin, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Molecular Genetics & Genomic Medicine|October 19, 2019
Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndromeMinna Luo, Li Cao, Zongfu Cao, et al.
Journal of Medical Genetics|May 30, 2024
ZFYVE19 deficiency: a ciliopathy involving failure of cell division, with cell deathJing Yang, Ya-Nan Zhang, Ren-Xue Wang, et al.
Blood|February 11, 2026
Nucleoplasmic ZNF467 condensates boost hematopoietic stem cell engraftment via ICAM1-mediated mechanical reprogrammingYandan Chen, Jinghao Shen, Zaisheng Lin, et al.
Plos Biology|March 2, 2023
Ependymal polarity defects coupled with disorganized ciliary beating drive abnormal cerebrospinal fluid flow and spine curvature in zebrafishHaibo Xie, Yunsi Kang, Junjun Liu, et al.
Chemical Science|April 3, 2023
Heparan sulfate glycomimetics <i>via</i> iterative assembly of "clickable" disaccharidesCangjie Yang, Yu Deng, Yang Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2021
Correction to: Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndromeMinna Luo, Zaisheng Lin, Tian Zhu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2021
Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndromeMinna Luo, Zaisheng Lin, Tian Zhu, et al.
The Journal of Clinical Investigation|October 30, 2025
Ciliopathy-related B9 protein complex regulates ciliary axonemal microtubule post-translational modifications and initiation of ciliogenesisRuida He, Yan Li, Minjun Jin, et al.
Pageof 7