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X C Li

Showing results (221-230 of 226) with videos related to

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Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|March 3, 2024
[Surgical treatment and prognosis analysis of hilar cholangiocarcinoma]X C Li, C X Li, H Zhang, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|July 1, 2022
[Efficacy and safety of neoadjuvant immunotherapy for hepatocellular carcinoma]Y X Xia, H Zhang, F Zhang, et al.
American Journal of Human Genetics|June 13, 1998
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|January 7, 2021
[Surgical treatment of primary liver cancer:a report of 10 966 cases]Y X Xia, F Zhang, X C Li, et al.
American Journal of Human Genetics|November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.
Oncogenesis|February 15, 2017
Integrative analyses of transcriptome sequencing identify novel functional lncRNAs in esophageal squamous cell carcinomaC-Q Li, G-W Huang, Z-Y Wu, et al.
Pageof 23

Showing results (221-230 of 226) with videos related to

Sort By:
Pageof 23
You have reached the last page of results.This site can display upto 226 results.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|March 3, 2024
[Surgical treatment and prognosis analysis of hilar cholangiocarcinoma]X C Li, C X Li, H Zhang, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|July 1, 2022
[Efficacy and safety of neoadjuvant immunotherapy for hepatocellular carcinoma]Y X Xia, H Zhang, F Zhang, et al.
American Journal of Human Genetics|June 13, 1998
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|January 7, 2021
[Surgical treatment of primary liver cancer:a report of 10 966 cases]Y X Xia, F Zhang, X C Li, et al.
American Journal of Human Genetics|November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.
Oncogenesis|February 15, 2017
Integrative analyses of transcriptome sequencing identify novel functional lncRNAs in esophageal squamous cell carcinomaC-Q Li, G-W Huang, Z-Y Wu, et al.
Pageof 23