Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma-Reference-Cited by-同舟云学术

Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma

Published:2015-08-11 Issue:8 Volume:10 Page:e0135643
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Kloss-Brandstätter Anita,Weissensteiner Hansi,Erhart Gertraud,Schäfer Georg,Forer Lukas,Schönherr Sebastian,Pacher Dominic,Seifarth Christof,Stöckl Andrea,Fendt Liane,Sottsas Irma,Klocker Helmut,Huck Christian W.,Rasse Michael,Kronenberg Florian,Kloss Frank R.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference69 articles.

1. Genetic and molecular alterations associated with oral squamous cell cancer (Review);M Perez-Sayans;Oncol Rep,2009

2. Sexual behaviours and the risk of head and neck cancers: a pooled analysis in the International Head and Neck Cancer Epidemiology (INHANCE) consortium;JE Heck;Int J Epidemiol,2010

3. Disparities in risk of and survival from oropharyngeal squamous cell carcinoma;CS Miller;Oral Surg Oral Med Oral Pathol Oral Radiol Endod,2003

4. Influence of marginal and segmental mandibular resection on the survival rate in patients with squamous cell carcinoma of the inferior parts of the oral cavity;D Wolff;J Craniomaxillofac Surg,2004

5. A compendium of human mitochondrial gene expression machinery with links to disease;TE Shutt;Environ Mol Mutagen,2010

Cited by 40 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mitochondrial point heteroplasmy: insights from deep-sequencing of human replicate samples;BMC Genomics;2024-01-10

2. Low-level point heteroplasmy detection in human mitogenomes amplified with different polymerases and sequenced on MiSeq FGx platform;Archives of Forensic Medicine and Criminology;2023-12-11

3. Identification of new variants in MTRNR1 and MTRNR2 genes using whole mitochondrial genome sequencing in a Taiwanese family with MERRF (myoclonic epilepsy with ragged-red fibers) syndrome;Hearing Research;2023-10

4. Capability of the iSeq 100 sequencing system from Illumina to detect low-level substitutions in the human mitochondrial genome;Forensic Science International: Genetics;2023-09

5. Sequencing Analysis of MUC6 and MUC16 Gene Fragments in Patients with Oropharyngeal Squamous Cell Carcinoma Reveals Novel Mutations: A Preliminary Study;Current Issues in Molecular Biology;2023-07-04