Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family
Authors
Keywords
Deafness, Apoptosis, Cochlea, Cell cycle and cell division, Transfection, Autosomal dominant traits, Guinea pigs, Polymerase chain reaction
Journal
PLoS One
Volume 10, Issue 7, Pages e0133522
Publisher
Public Library of Science (PLoS)
Online
2015-07-22
DOI
10.1371/journal.pone.0133522
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Non-syndromic hereditary sensorineural hearing loss: review of the genes involved
- (2014) F Stelma et al. JOURNAL OF LARYNGOLOGY AND OTOLOGY
- Characterization of Transcriptomes of Cochlear Inner and Outer Hair Cells
- (2014) H. Liu et al. JOURNAL OF NEUROSCIENCE
- The ORC/Cdc6/MCM2–7 complex, a new power player for regulated helicase loading
- (2013) Alberto Riera et al. CELL CYCLE
- Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss
- (2013) Yali Zhao et al. PLoS One
- Mutation of the ATP-gated P2X2 receptor leads to progressive hearing loss and increased susceptibility to noise
- (2013) D. Yan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The Minichromosome Maintenance Replicative Helicase
- (2013) S. D. Bell et al. Cold Spring Harbor Perspectives in Biology
- Whole exome sequencing identifies a novelDFNA9mutation, C162Y
- (2012) J Gao et al. CLINICAL GENETICS
- Minichromosome Maintenance 2 Bound with Retroviral Gp70 Is Localized to Cytoplasm and Enhances DNA-Damage-Induced Apoptosis
- (2012) Shinya Abe et al. PLoS One
- Overexpression of MCM2 in myelodysplastic syndromes: Association with bone marrow cell apoptosis and peripheral cytopenia
- (2011) Shiho Suzuki et al. EXPERIMENTAL AND MOLECULAR PATHOLOGY
- Apoptosis in acquired and genetic hearing impairment: The programmed death of the hair cell
- (2011) Ken Op de Beeck et al. HEARING RESEARCH
- Comprehensive comparison of three commercial human whole-exome capture platforms
- (2011) Asan et al. GENOME BIOLOGY
- Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51
- (2010) Tom Walsh et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Whole-exome sequencing: a powerful technique for identifying novel genes of complex disorders
- (2010) SS Sanders CLINICAL GENETICS
- Novel genomic techniques open new avenues in the analysis of monogenic disorders
- (2010) Gregor Kuhlenbäumer et al. HUMAN MUTATION
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Function and Expression Pattern of Nonsyndromic Deafness Genes
- (2009) Nele Hilgert et al. CURRENT MOLECULAR MEDICINE
- A novel role for acinus and MCM2 as host-specific signaling enhancers of DNA-damage-induced apoptosis in association with viral protein gp70
- (2008) Maki Hasegawa et al. LEUKEMIA RESEARCH
- The Mcm2-7 Complex Has In Vitro Helicase Activity
- (2008) Matthew L. Bochman et al. MOLECULAR CELL
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started