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Substitution mutation

Optimal Codon Identities in Bacteria: Implications from the Conflicting Results of Two Different Methods

Bin Wang, Zhu-Qing Shao, [ ... ], Jian-Qun Chen

Impact of the HIV-1 env Genetic Context outside HR1–HR2 on Resistance to the Fusion Inhibitor Enfuvirtide and Viral Infectivity in Clinical Isolates

Franky Baatz, Monique Nijhuis, [ ... ], Danielle Perez Bercoff

Molecular Modelling of the Emergence of Azole Resistance in Mycosphaerella graminicola

Jonathan G. L. Mullins, Josie E. Parker, [ ... ], Steven L. Kelly

The Congenital Cataract-Linked G61C Mutation Destabilizes γD-Crystallin and Promotes Non-Native Aggregation

Wang Zhang, Hong-Chen Cai, [ ... ], Yong-Bin Yan

RET Germline Mutations Identified by Exome Sequencing in a Chinese Multiple Endocrine Neoplasia Type 2A/Familial Medullary Thyroid Carcinoma Family

Xiao-Ping Qi, Ju-Ming Ma, [ ... ], Xian-Ning Zhang

In Silico and In Vitro Investigations of the Mutability of Disease-Causing Missense Mutation Sites in Spermine Synthase

Zhe Zhang, Joy Norris, Charles Schwartz, Emil Alexov

Screen for IDH1, IDH2, IDH3, D2HGDH and L2HGDH Mutations in Glioblastoma

Daniel Krell, Mawuelikem Assoku, [ ... ], Chiara Bardella

Engineering of Insulin Receptor Isoform-Selective Insulin Analogues

Tine Glendorf, Carsten E. Stidsen, [ ... ], Thomas Kjeldsen

Variation in NOD2 Augments Th2- and Th17 Responses to Myelin Basic Protein in Multiple Sclerosis

Chris Juul Hedegaard, Christian Enevold, [ ... ], Claus Henrik Nielsen

Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis

Lin Li, Xueshan Xiao, [ ... ], J. Fielding Hejtmancik

An ENU-Mutagenesis Screen in the Mouse: Identification of Novel Developmental Gene Functions

Carolien Wansleeben, Léon van Gurp, [ ... ], Frits Meijlink

Dynamic Diagnosis of Familial Prion Diseases Supports the β2-α2 Loop as a Universal Interference Target

Massimiliano Meli, Maria Gasset, Giorgio Colombo

Evolutionary Analyses of Entire Genomes Do Not Support the Association of mtDNA Mutations with Ras/MAPK Pathway Syndromes

Alberto Gómez-Carballa, María Cerezo, [ ... ], Antonio Salas

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