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Mutation

The Evolution of Heterogeneities Altered by Mutational Robustness, Gene Expression Noise and Bottlenecks in Gene Regulatory Networks

Zhihua Zhang

The Mouse MC13 Mutant Is a Novel ENU Mutation in Collagen Type II, Alpha 1

Megan Cionni, Chelsea Menke, Rolf W. Stottmann

An Integrative Analysis of PIK3CA Mutation, PTEN, and INPP4B Expression in Terms of Trastuzumab Efficacy in HER2-Positive Breast Cancer

Aiko Sueta, Yutaka Yamamoto, [ ... ], Hirotaka Iwase

Detection of SRSF2-P95 Mutation by High-Resolution Melting Curve Analysis and Its Effect on Prognosis in Myelodysplastic Syndrome

Jiang Lin, Jing Yang, [ ... ], Jun Qian

Two Desmin Gene Mutations Associated with Myofibrillar Myopathies in Polish Families

Jakub Piotr Fichna, Justyna Karolczak, [ ... ], Cezary Zekanowski

Characterization of the MeCP2^R168X Knockin Mouse Model for Rett Syndrome

Eike Wegener, Cornelia Brendel, [ ... ], Peter Huppke

Characterization of G6PD Genotypes and Phenotypes on the Northwestern Thailand-Myanmar Border

Germana Bancone, Cindy S. Chu, [ ... ], François H. Nosten

Glucocerebrosidase Gene Mutations Associated with Parkinson's Disease: A Meta-Analysis in a Chinese population

Jia Chen, Wei Li, [ ... ], Zhi-qiang Xu

One-Step Biosynthesis of α-Keto-γ-Methylthiobutyric Acid from L-Methionine by an Escherichia coli Whole-Cell Biocatalyst Expressing an Engineered L-Amino Acid Deaminase from Proteus vulgaris

Gazi Sakir Hossain, Jianghua Li, [ ... ], Jian Chen

Integrated Analysis of Whole Genome and Transcriptome Sequencing Reveals Diverse Transcriptomic Aberrations Driven by Somatic Genomic Changes in Liver Cancers

Yuichi Shiraishi, Akihiro Fujimoto, [ ... ], Hidewaki Nakagawa

Live Cell Imaging Reveals Novel Functions of Salmonella enterica SPI2-T3SS Effector Proteins in Remodeling of the Host Cell Endosomal System

Roopa Rajashekar, David Liebl, [ ... ], Michael Hensel

Profiling of Exome Mutations Associated with Progression of HBV-Related Hepatocellular Carcinoma

Hyun Goo Woo, Soon Sun Kim, [ ... ], Jae Youn Cheong

A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract

Yanan Zhu, Hao Yu, [ ... ], Ke Yao

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