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Mutation

Analysis of Spo0M function in Bacillus subtilis

Luz Adriana Vega-Cabrera, Adán Guerrero, [ ... ], Liliana Pardo-López

Evaluation of Aminoglycoside and Non-Aminoglycoside Compounds for Stop-Codon Readthrough Therapy in Four Lysosomal Storage Diseases

Marta Gómez-Grau, Elena Garrido, [ ... ], Lluïsa Vilageliu

A Putative Transcription Factor MYT1 Is Required for Female Fertility in the Ascomycete Gibberella zeae

Yang Lin, Hokyoung Son, [ ... ], Yin-Won Lee

High Mitochondrial DNA Stability in B-Cell Chronic Lymphocytic Leukemia

María Cerezo, Hans-Jürgen Bandelt, [ ... ], Antonio Salas

Improved Classification of Lung Cancer Using Radial Basis Function Neural Network with Affine Transforms of Voss Representation

Emmanuel Adetiba, Oludayo O. Olugbara

Bluetongue Virus Nonstructural Protein NS3/NS3a Is Not Essential for Virus Replication

René G. P. van Gennip, Sandra G. P. van de Water, Piet A. van Rijn

Mutation at Intronic Repeats of the Ataxia-Telangiectasia Mutated (ATM) Gene and ATM Protein Loss in Primary Gastric Cancer with Microsatellite Instability

Hee Sung Kim, Seung Im Choi, [ ... ], Woo Ho Kim

Adaptation of an L-Proline Adenylation Domain to Use 4-Propyl-L-Proline in the Evolution of Lincosamide Biosynthesis

Stanislav Kadlčík, Tomáš Kučera, [ ... ], Jiří Janata

Expression Levels of the ABCG2 Multidrug Transporter in Human Erythrocytes Correspond to Pharmacologically Relevant Genetic Variations

Ildikó Kasza, György Várady, [ ... ], Balázs Sarkadi

Escherichia coli Frameshift Mutation Rate Depends on the Chromosomal Context but Not on the GATC Content Near the Mutation Site

Mariana A. Martina, Elisa M. E. Correa, Carlos E. Argaraña, José L. Barra

The Ability to Form Homodimers Is Essential for RDM1 to Function in RNA-Directed DNA Methylation

Taku Sasaki, Zdravko J. Lorković, [ ... ], Marjori Matzke

Analysis of al-2 Mutations in Neurospora

Violeta Díaz-Sánchez, Alejandro F. Estrada, [ ... ], Javier Avalos

Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome

Alessandro Pecci, Ginevra Biino, [ ... ], for the Italian Registry for MYH9 -releated diseases

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