Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family

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