Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Xiang Deng

Showing results (181-190 of 220) with videos related to

Pageof 22
Sort By:
Neurogenetics|September 7, 2014
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathySenda Ajroud-Driss, Faisal Fecto, Kaouther Ajroud, et al.
Cancer Management and Research|January 4, 2018
Programmed death-ligand 1 expression correlates with diminished CD8+ T cell infiltration and predicts poor prognosis in anal squamous cell carcinoma patientsYu-Jie Zhao, Wei-Peng Sun, Jian-Hong Peng, et al.
International Journal of Biological Macromolecules|February 10, 2020
Sodium tanshinone IIA sulfonate protects against Aβ<sub>1-42</sub>-induced cellular toxicity by modulating Aβ-degrading enzymes in HT22 cellsXiao-Qi Liu, Ya-Xiang Deng, Zhao Dai, et al.
Zhonghua Yi Xue Za Zhi|September 24, 2005
[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6]Yu-hu Zhang, Bei-sha Tang, Ji-feng Guo, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 11, 2019
Glutathione Reductase Promotes Fungal Clearance and Suppresses Inflammation during Systemic <i>Candida albicans</i> Infection in MiceVictoria Y Kim, Abel Batty, Jinhui Li, et al.
Neurology. Genetics|April 29, 2016
Compound heterozygote mutations in SPG7 in a family with adult-onset primary lateral sclerosisYi Yang, Lei Zhang, David R Lynch, et al.
Oncotargets and Therapy|December 5, 2017
Lymphocyte-to-monocyte ratio before chemoradiotherapy represents a prognostic predictor for locally advanced rectal cancerYu-Xiang Deng, Jun-Zhong Lin, Jian-Hong Peng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2019
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humansYue-Qiu Tan, Chaofeng Tu, Lanlan Meng, et al.
Communications Biology|March 26, 2021
Efficacy and long-term safety of CRISPR/Cas9 genome editing in the SOD1-linked mouse models of ALSHan-Xiang Deng, Hong Zhai, Yong Shi, et al.
Archives of Neurology|August 10, 2011
Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutationsHan-Xiang Deng, Eileen H Bigio, Hong Zhai, et al.
Pageof 22

Showing results (181-190 of 220) with videos related to

Sort By:
Pageof 22
Neurogenetics|September 7, 2014
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathySenda Ajroud-Driss, Faisal Fecto, Kaouther Ajroud, et al.
Cancer Management and Research|January 4, 2018
Programmed death-ligand 1 expression correlates with diminished CD8+ T cell infiltration and predicts poor prognosis in anal squamous cell carcinoma patientsYu-Jie Zhao, Wei-Peng Sun, Jian-Hong Peng, et al.
International Journal of Biological Macromolecules|February 10, 2020
Sodium tanshinone IIA sulfonate protects against Aβ<sub>1-42</sub>-induced cellular toxicity by modulating Aβ-degrading enzymes in HT22 cellsXiao-Qi Liu, Ya-Xiang Deng, Zhao Dai, et al.
Zhonghua Yi Xue Za Zhi|September 24, 2005
[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6]Yu-hu Zhang, Bei-sha Tang, Ji-feng Guo, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 11, 2019
Glutathione Reductase Promotes Fungal Clearance and Suppresses Inflammation during Systemic <i>Candida albicans</i> Infection in MiceVictoria Y Kim, Abel Batty, Jinhui Li, et al.
Neurology. Genetics|April 29, 2016
Compound heterozygote mutations in SPG7 in a family with adult-onset primary lateral sclerosisYi Yang, Lei Zhang, David R Lynch, et al.
Oncotargets and Therapy|December 5, 2017
Lymphocyte-to-monocyte ratio before chemoradiotherapy represents a prognostic predictor for locally advanced rectal cancerYu-Xiang Deng, Jun-Zhong Lin, Jian-Hong Peng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2019
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humansYue-Qiu Tan, Chaofeng Tu, Lanlan Meng, et al.
Communications Biology|March 26, 2021
Efficacy and long-term safety of CRISPR/Cas9 genome editing in the SOD1-linked mouse models of ALSHan-Xiang Deng, Hong Zhai, Yong Shi, et al.
Archives of Neurology|August 10, 2011
Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutationsHan-Xiang Deng, Eileen H Bigio, Hong Zhai, et al.
Pageof 22