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Mingyan Fang

Showing results (61-70 of 71) with videos related to

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Annals of Neurology|November 4, 2015
DNAJC6 Mutations Associated With Early-Onset Parkinson's DiseaseSimone Olgiati, Marialuisa Quadri, Mingyan Fang, et al.
Cell Reports. Medicine|December 9, 2022
A population-based study of precision health assessments using multi-omics network-derived biological functional modulesWei Zhang, Ziyun Wan, Xiaoyu Li, et al.
Genomics, Proteomics & Bioinformatics|September 27, 2024
Whole-genome Sequencing Association Analysis of Quantitative Platelet Traits in A Large Cohort of β-thalassemiaXingmin Wang, Qianqian Zhang, Xianming Chen, et al.
Annals of Neurology|March 29, 2020
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic NeuropathyLeonardo Caporali, Stefania Magri, Andrea Legati, et al.
JCI Insight|August 1, 2024
An atypical form of 60S ribosomal subunit in Diamond-Blackfan anemia linked to RPL17 variantsFlorence Fellmann, Carol Saunders, Marie-Françoise O'Donohue, et al.
The Journal of Clinical Investigation|December 8, 2015
POPDC1(S201F) causes muscular dystrophy and arrhythmia by affecting protein traffickingRoland F R Schindler, Chiara Scotton, Jianguo Zhang, et al.
The Journal of Experimental Medicine|December 25, 2016
Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiencyHassan Abolhassani, Emily S J Edwards, Aydan Ikinciogullari, et al.
Brain : a Journal of Neurology|February 26, 2016
LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearanceCristina Dallabona, Truus E M Abbink, Rosalba Carrozzo, et al.
Annals of the Rheumatic Diseases|May 19, 2019
T cell receptor β repertoires as novel diagnostic markers for systemic lupus erythematosus and rheumatoid arthritisXiao Liu, Wei Zhang, Ming Zhao, et al.
Neurology. Genetics|December 30, 2020
Ethnicity-related DMD Genotype Landscapes in European and Non-European CountriesRita Selvatici, Rachele Rossi, Fernanda Fortunato, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Annals of Neurology|November 4, 2015
DNAJC6 Mutations Associated With Early-Onset Parkinson's DiseaseSimone Olgiati, Marialuisa Quadri, Mingyan Fang, et al.
Cell Reports. Medicine|December 9, 2022
A population-based study of precision health assessments using multi-omics network-derived biological functional modulesWei Zhang, Ziyun Wan, Xiaoyu Li, et al.
Genomics, Proteomics & Bioinformatics|September 27, 2024
Whole-genome Sequencing Association Analysis of Quantitative Platelet Traits in A Large Cohort of β-thalassemiaXingmin Wang, Qianqian Zhang, Xianming Chen, et al.
Annals of Neurology|March 29, 2020
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic NeuropathyLeonardo Caporali, Stefania Magri, Andrea Legati, et al.
JCI Insight|August 1, 2024
An atypical form of 60S ribosomal subunit in Diamond-Blackfan anemia linked to RPL17 variantsFlorence Fellmann, Carol Saunders, Marie-Françoise O'Donohue, et al.
The Journal of Clinical Investigation|December 8, 2015
POPDC1(S201F) causes muscular dystrophy and arrhythmia by affecting protein traffickingRoland F R Schindler, Chiara Scotton, Jianguo Zhang, et al.
The Journal of Experimental Medicine|December 25, 2016
Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiencyHassan Abolhassani, Emily S J Edwards, Aydan Ikinciogullari, et al.
Brain : a Journal of Neurology|February 26, 2016
LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearanceCristina Dallabona, Truus E M Abbink, Rosalba Carrozzo, et al.
Annals of the Rheumatic Diseases|May 19, 2019
T cell receptor β repertoires as novel diagnostic markers for systemic lupus erythematosus and rheumatoid arthritisXiao Liu, Wei Zhang, Ming Zhao, et al.
Neurology. Genetics|December 30, 2020
Ethnicity-related DMD Genotype Landscapes in European and Non-European CountriesRita Selvatici, Rachele Rossi, Fernanda Fortunato, et al.
Pageof 8