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

Mingyan Fang

Showing results (21-30 of 71) with videos related to

Pageof 8
Sort By:
Plos One|March 31, 2022
Calculating and comparing codon usage values in rare disease genes highlights codon clustering with disease-and tissue- specific hierarchyRachele Rossi, Mingyan Fang, Lin Zhu, et al.
Diabetes Research and Clinical Practice|April 5, 2014
Lessons from whole-exome sequencing in MODYX familiesPetra Dusatkova, Mingyan Fang, Stepanka Pruhova, et al.
TH Open : Companion Journal to Thrombosis and Haemostasis|December 30, 2020
Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense <i>RASGRP2</i> MutationJulia Körholz, Nadja Lucas, Franziska Boiti, et al.
Neurogenetics|August 27, 2013
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3Ginevra Zanni, Chiara Scotton, Chiara Passarelli, et al.
Molecular Genetics and Metabolism|September 27, 2012
A novel homozygous mutation in SUCLA2 gene identified by exome sequencingCostanza Lamperti, Mingyan Fang, Federica Invernizzi, et al.
NPJ Genomic Medicine|April 2, 2026
Population-scale genomic screening reveals high frequency of actionable secondary findings in Chinese newbornsYushan Huang, Ya Gao, Zonghao Duan, et al.
Aging Cell|January 2, 2025
Age-Related Dynamics and Spectral Characteristics of the TCRβ Repertoire in Healthy Children: Implications for Immune AgingMingyan Fang, Yu Miao, Lin Zhu, et al.
Frontiers in Genetics|May 13, 2025
Shared genetic features inference among hypoxia-ischemia diseases in the presence of heterogenous omics data based on a novel risk assessment methodYifan Zhang, Jianfeng Liu, Zhuoma Basang, et al.
Cardiology|May 12, 2017
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada SyndromeFrancesca Gualandi, Fatima Zaraket, Michele Malagù, et al.
Journal of Translational Medicine|February 24, 2023
Integrated multi-omics analyses and functional validation reveal TTK as a novel EMT activator for endometrial cancerYu Miao, Yosuke Konno, Baojin Wang, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
Plos One|March 31, 2022
Calculating and comparing codon usage values in rare disease genes highlights codon clustering with disease-and tissue- specific hierarchyRachele Rossi, Mingyan Fang, Lin Zhu, et al.
Diabetes Research and Clinical Practice|April 5, 2014
Lessons from whole-exome sequencing in MODYX familiesPetra Dusatkova, Mingyan Fang, Stepanka Pruhova, et al.
TH Open : Companion Journal to Thrombosis and Haemostasis|December 30, 2020
Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense <i>RASGRP2</i> MutationJulia Körholz, Nadja Lucas, Franziska Boiti, et al.
Neurogenetics|August 27, 2013
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3Ginevra Zanni, Chiara Scotton, Chiara Passarelli, et al.
Molecular Genetics and Metabolism|September 27, 2012
A novel homozygous mutation in SUCLA2 gene identified by exome sequencingCostanza Lamperti, Mingyan Fang, Federica Invernizzi, et al.
NPJ Genomic Medicine|April 2, 2026
Population-scale genomic screening reveals high frequency of actionable secondary findings in Chinese newbornsYushan Huang, Ya Gao, Zonghao Duan, et al.
Aging Cell|January 2, 2025
Age-Related Dynamics and Spectral Characteristics of the TCRβ Repertoire in Healthy Children: Implications for Immune AgingMingyan Fang, Yu Miao, Lin Zhu, et al.
Frontiers in Genetics|May 13, 2025
Shared genetic features inference among hypoxia-ischemia diseases in the presence of heterogenous omics data based on a novel risk assessment methodYifan Zhang, Jianfeng Liu, Zhuoma Basang, et al.
Cardiology|May 12, 2017
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada SyndromeFrancesca Gualandi, Fatima Zaraket, Michele Malagù, et al.
Journal of Translational Medicine|February 24, 2023
Integrated multi-omics analyses and functional validation reveal TTK as a novel EMT activator for endometrial cancerYu Miao, Yosuke Konno, Baojin Wang, et al.
Pageof 8