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Sha Tang

Showing results (291-300 of 448) with videos related to

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Biochemical and Biophysical Research Communications|December 5, 2012
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosisWen-Juan Guan, Jun-Ling Wang, Yu-Tao Liu, et al.
Mayo Clinic Proceedings|February 10, 2015
Whole-exome sequencing as a diagnostic tool in a family with episodic ataxia type 1Pawel Tacik, Kimberly J Guthrie, Audrey J Strongosky, et al.
Neuroscience Letters|July 7, 2010
FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patientsLin-zi Luo, Qian Xu, Ji-feng Guo, et al.
Neuroscience Letters|April 17, 2012
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's diseaseJin-yong Tian, Ji-feng Guo, Lei Wang, et al.
Prenatal Diagnosis|July 7, 2015
Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomaliesChristina L Alamillo, Zöe Powis, Kelly Farwell, et al.
Chinese Medical Journal|January 17, 2018
Screening for <i>SH3TC2, PMP2</i>, and <i>BSCL2</i> Variants in a Cohort of Chinese Patients with Charcot-Marie-ToothXin Zhao, Ming-Ming Jiang, Yi-Zhou Yan, et al.
Immunology Letters|February 5, 2022
Clinical significance and role of CXCL16 in anti-neutrophil cytoplasmic autoantibody-associated vasculitisWenjie Li, Qiwu Zhang, Lijiao Xie, et al.
Journal of Thrombosis and Thrombolysis|November 28, 2012
TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese populationJie Feng, Yun-Hai Liu, Qi-Dong Yang, et al.
Human Mutation|January 21, 2017
Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and ReclassificationsErica D Smith, Kelly Radtke, Mari Rossi, et al.
Parkinsonism & Related Disorders|August 19, 2018
Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's diseaseShu-Ying Liu, Zheng Zheng, Zhu-Qin Gu, et al.
Pageof 45

Showing results (291-300 of 448) with videos related to

Sort By:
Pageof 45
Biochemical and Biophysical Research Communications|December 5, 2012
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosisWen-Juan Guan, Jun-Ling Wang, Yu-Tao Liu, et al.
Mayo Clinic Proceedings|February 10, 2015
Whole-exome sequencing as a diagnostic tool in a family with episodic ataxia type 1Pawel Tacik, Kimberly J Guthrie, Audrey J Strongosky, et al.
Neuroscience Letters|July 7, 2010
FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patientsLin-zi Luo, Qian Xu, Ji-feng Guo, et al.
Neuroscience Letters|April 17, 2012
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's diseaseJin-yong Tian, Ji-feng Guo, Lei Wang, et al.
Prenatal Diagnosis|July 7, 2015
Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomaliesChristina L Alamillo, Zöe Powis, Kelly Farwell, et al.
Chinese Medical Journal|January 17, 2018
Screening for <i>SH3TC2, PMP2</i>, and <i>BSCL2</i> Variants in a Cohort of Chinese Patients with Charcot-Marie-ToothXin Zhao, Ming-Ming Jiang, Yi-Zhou Yan, et al.
Immunology Letters|February 5, 2022
Clinical significance and role of CXCL16 in anti-neutrophil cytoplasmic autoantibody-associated vasculitisWenjie Li, Qiwu Zhang, Lijiao Xie, et al.
Journal of Thrombosis and Thrombolysis|November 28, 2012
TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese populationJie Feng, Yun-Hai Liu, Qi-Dong Yang, et al.
Human Mutation|January 21, 2017
Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and ReclassificationsErica D Smith, Kelly Radtke, Mari Rossi, et al.
Parkinsonism & Related Disorders|August 19, 2018
Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's diseaseShu-Ying Liu, Zheng Zheng, Zhu-Qin Gu, et al.
Pageof 45