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Mutation

Genotyping of Fanconi Anemia Patients by Whole Exome Sequencing: Advantages and Challenges

Kerstin Knies, Beatrice Schuster, [ ... ], Detlev Schindler

A Mouse Model for Osseous Heteroplasia

Michael T. Cheeseman, Kate Vowell, [ ... ], Jo Peters

Non-Random mtDNA Segregation Patterns Indicate a Metastable Heteroplasmic Segregation Unit in m.3243A>G Cybrid Cells

Anton K. Raap, Roshan S. Jahangir Tafrechi, [ ... ], George M. C. Janssen

PFunkel: Efficient, Expansive, User-Defined Mutagenesis

Elad Firnberg, Marc Ostermeier

Anti-Campylobacter Activities and Resistance Mechanisms of Natural Phenolic Compounds in Campylobacter

Anja Klančnik, Sonja Smole Možina, Qijing Zhang

Mutation Scanning Using MUT-MAP, a High-Throughput, Microfluidic Chip-Based, Multi-Analyte Panel

Rajesh Patel, Alison Tsan, [ ... ], Rajiv Raja

Differentiating Inbred Mouse Strains from Each Other and Those with Single Gene Mutations Using Hair Proteomics

Robert H. Rice, Katie M. Bradshaw, [ ... ], John P. Sundberg

Genome-Wide Survey of Pseudogenes in 80 Fully Re-sequenced Arabidopsis thaliana Accessions

Long Wang, Weina Si, [ ... ], Sihai Yang

A Meta-Analysis of the Relationship between FGFR3 and TP53 Mutations in Bladder Cancer

Yann Neuzillet, Xavier Paoletti, [ ... ], François Radvanyi

A Novel SERPINA1 Mutation Causing Serum Alpha₁-Antitrypsin Deficiency

Darren N. Saunders, Elizabeth A. Tindall, [ ... ], Vanessa M. Hayes

Multiple Mechanisms Contribute to Leakiness of a Frameshift Mutation in Canine Cone-Rod Dystrophy

Keiko Miyadera, Ian Brierley, [ ... ], David R. Sargan

Exome Sequencing Identifies a Founder Frameshift Mutation in an Alternative Exon of USH1C as the Cause of Autosomal Recessive Retinitis Pigmentosa with Late-Onset Hearing Loss

Samer Khateb, Lina Zelinger, [ ... ], Dror Sharon

Whole Genome Characterization, Phylogenetic and Genome Signature Analysis of Human Pandemic H1N1 Virus in Thailand, 2009–2012

Jarika Makkoch, Kamol Suwannakarn, [ ... ], Yong Poovorawan

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