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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 3, 2006
[Lecithin-cholesterol acyltransferase gene 608C/T polymorphism associated with atherosclerotic cerebral infarction]
Xiao-yan Zhu, Hong-wei Xu, Rong-yao Hou, et al.
Acta Biomaterialia
|
April 1, 2024
Neuron-targeted liposomal coenzyme Q10 attenuates neuronal ferroptosis after subarachnoid hemorrhage by activating the ferroptosis suppressor protein 1/coenzyme Q10 system
Zheng Peng, Yi-Nan Ding, Zheng-Mao Yang, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
September 8, 2019
Preliminary study of hsa-miR-626 change in the cerebrospinal fluid of Parkinson's disease patients
Li-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Journal of Genetic Counseling
|
December 6, 2013
Diagnostic exome sequencing identifies two novel IQSEC2 mutations associated with X-linked intellectual disability with seizures: implications for genetic counseling and clinical diagnosis
Stephanie K Gandomi, K D Farwell Gonzalez, M Parra, et al.
Plos One
|
February 3, 2017
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels
Holly LaDuca, Kelly D Farwell, Huy Vuong, et al.
Journal of Materials Science. Materials in Medicine
|
May 27, 2014
Fabrication, characterization, and biocompatibility of ethyl cellulose/carbonated hydroxyapatite composite coatings on Ti6Al4V
Bo Tian, Sha Tang, Yang Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 11, 2006
[Cloning to rule out 10 candidate genes located in chromosome 12q24 for Charcot-Marie-Tooth disease type 2L]
Ru-xu Zhang, Bei-sha Tang, Xiao-hong Zi, et al.
Neurology India
|
July 18, 2013
Gluten ataxia of sporadic and hereditary cerebellar ataxia in patients from mainland China
Wen-Juan Guan, Xin-Jian Liu, Bei-Sha Tang, et al.
Frontiers in Neuroanatomy
|
November 23, 2017
Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients
Yan Tang, Xue Xiao, Hua Xie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 5, 2010
Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese population
Qi-Ying Sun, Ji-Feng Guo, Lei Wang, et al.
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Search research articles
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Showing results (191-200 of 448) with videos related to
Sort By:
Page
of 45
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
August 3, 2006
[Lecithin-cholesterol acyltransferase gene 608C/T polymorphism associated with atherosclerotic cerebral infarction]
Xiao-yan Zhu, Hong-wei Xu, Rong-yao Hou, et al.
Acta Biomaterialia
|
April 1, 2024
Neuron-targeted liposomal coenzyme Q10 attenuates neuronal ferroptosis after subarachnoid hemorrhage by activating the ferroptosis suppressor protein 1/coenzyme Q10 system
Zheng Peng, Yi-Nan Ding, Zheng-Mao Yang, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
September 8, 2019
Preliminary study of hsa-miR-626 change in the cerebrospinal fluid of Parkinson's disease patients
Li-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Journal of Genetic Counseling
|
December 6, 2013
Diagnostic exome sequencing identifies two novel IQSEC2 mutations associated with X-linked intellectual disability with seizures: implications for genetic counseling and clinical diagnosis
Stephanie K Gandomi, K D Farwell Gonzalez, M Parra, et al.
Plos One
|
February 3, 2017
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels
Holly LaDuca, Kelly D Farwell, Huy Vuong, et al.
Journal of Materials Science. Materials in Medicine
|
May 27, 2014
Fabrication, characterization, and biocompatibility of ethyl cellulose/carbonated hydroxyapatite composite coatings on Ti6Al4V
Bo Tian, Sha Tang, Yang Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 11, 2006
[Cloning to rule out 10 candidate genes located in chromosome 12q24 for Charcot-Marie-Tooth disease type 2L]
Ru-xu Zhang, Bei-sha Tang, Xiao-hong Zi, et al.
Neurology India
|
July 18, 2013
Gluten ataxia of sporadic and hereditary cerebellar ataxia in patients from mainland China
Wen-Juan Guan, Xin-Jian Liu, Bei-Sha Tang, et al.
Frontiers in Neuroanatomy
|
November 23, 2017
Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients
Yan Tang, Xue Xiao, Hua Xie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 5, 2010
Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese population
Qi-Ying Sun, Ji-Feng Guo, Lei Wang, et al.
Page
of 45