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Biological databases

Whole Proteome Analyses on Ruminiclostridium cellulolyticum Show a Modulation of the Cellulolysis Machinery in Response to Cellulosic Materials with Subtle Differences in Chemical and Structural Properties

Nelly Badalato, Alain Guillot, [ ... ], Ariane Bize

A Novel Single Nucleotide T980C Polymorphism in the Human Carboxypeptidase E Gene Results in Loss of Neuroprotective Function

Lin Cong, Yong Cheng, [ ... ], Y. Peng Loh

Characterization of the Drug Resistance Profiles of Patients Infected with CRF07_BC Using Phenotypic Assay and Ultra-Deep Pyrosequencing

Szu-Wei Huang, Wei-You Li, [ ... ], Yi-Ming Arthur Chen

Polymorphisms and Mutational Covariation Associated with Death in a Prospective Cohort of HIV/AIDS Patients Receiving Long-Term ART in China

Pengtao Liu, Yi Feng, [ ... ], Yuhua Ruan

DNA Metabarcoding of Amazonian Ichthyoplankton Swarms

M. E. Maggia, Y. Vigouroux, [ ... ], C. Mariac

Critical Features of Fragment Libraries for Protein Structure Prediction

Raphael Trevizani, Fábio Lima Custódio, Karina Baptista dos Santos, Laurent Emmanuel Dardenne

Rare Synaptogenesis-Impairing Mutations in SLITRK5 Are Associated with Obsessive Compulsive Disorder

Minseok Song, Carol A. Mathews, [ ... ], Charles E. Glatt

Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy

Yadi Li, Jie Li, [ ... ], Xiangming Guo

Nitrosothiol-Trapping-Based Proteomic Analysis of S-Nitrosylation in Human Lung Carcinoma Cells

Shani Ben-Lulu, Tamar Ziv, Pnina Weisman-Shomer, Moran Benhar

Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies

Hyun-Seok Jin, Jeonhyun Kim, [ ... ], Cha Gon Lee

Assessment of Common and Emerging Bioinformatics Pipelines for Targeted Metagenomics

Léa Siegwald, Hélène Touzet, [ ... ], Ségolène Caboche

Development of a Feature and Template-Assisted Assembler and Application to the Analysis of a Foot-and-Mouth Disease Virus Genotyping Microarray

Roger W. Barrette, Jessica M. Rowland, Frederic R. Grau, Michael T. McIntosh

Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing

Marta de Castro-Miró, Raul Tonda, [ ... ], Roser Gonzàlez-Duarte

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