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PLOS Genetics - Číslo 2/2010

Review

32767
Molecular Poltergeists: Mitochondrial DNA Copies () in Sequenced Nuclear Genomes

Perspective

32767
Wing Patterns in the Mist
Nucleoporins and Transcription: New Connections, New Questions

Research Article

32767
Nuclear Pore Proteins Nup153 and Megator Define Transcriptionally Active Regions in the Genome
The Scale of Population Structure in
Allelic Exchange of Pheromones and Their Receptors Reprograms Sexual Identity in
Genetic and Functional Dissection of and in Age-Related Macular Degeneration
A Single Nucleotide Polymorphism within the Acetyl-Coenzyme A Carboxylase Beta Gene Is Associated with Proteinuria in Patients with Type 2 Diabetes
The Genetic Interpretation of Area under the ROC Curve in Genomic Profiling
Genome-Wide Association Study in Asian Populations Identifies Variants in and Associated with Systemic Lupus Erythematosus
Cdk2 Is Required for p53-Independent G/M Checkpoint Control
Uncoupling of Satellite DNA and Centromeric Function in the Genus
Genomic Hotspots for Adaptation: The Population Genetics of Müllerian Mimicry in the Clade
Use of DNA–Damaging Agents and RNA Pooling to Assess Expression Profiles Associated with and Mutation Status in Familial Breast Cancer Patients
Cheating by Exploitation of Developmental Prestalk Patterning in
Replication and Active Demethylation Represent Partially Overlapping Mechanisms for Erasure of H3K4me3 in Budding Yeast
Cdk1 Targets Srs2 to Complete Synthesis-Dependent Strand Annealing and to Promote Recombinational Repair
A Genome-Wide Association Study Identifies Susceptibility Variants for Type 2 Diabetes in Han Chinese
Genome-Wide Identification of Susceptibility Alleles for Viral Infections through a Population Genetics Approach
Transcriptional Rewiring of the Sex Determining Gene Duplicate by Transposable Elements
Genomic Hotspots for Adaptation: The Population Genetics of Müllerian Mimicry in
Proteasome Nuclear Activity Affects Chromosome Stability by Controlling the Turnover of Mms22, a Protein Important for DNA Repair
Deletion of the Huntingtin Polyglutamine Stretch Enhances Neuronal Autophagy and Longevity in Mice
Structure, Function, and Evolution of the spp. Genome
Human and Non-Human Primate Genomes Share Hotspots of Positive Selection
A Kinase-Independent Role for the Rad3-Rad26 Complex in Recruitment of Tel1 to Telomeres in Fission Yeast
Analysis of the Genome and Transcriptome Uncovers Unique Strategies to Cause Legionnaires' Disease
Molecular Evolution and Functional Characterization of Insulin-Like Peptides
Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags
DNA Binding of Centromere Protein C (CENPC) Is Stabilized by Single-Stranded RNA
Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy
Mutations in , Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease
Genome-Wide Identification of Binding Sites Defines Distinct Functions for PHA-4/FOXA in Development and Environmental Response
Ku Regulates the Non-Homologous End Joining Pathway Choice of DNA Double-Strand Break Repair in Human Somatic Cells

PLOS Genetics

2010 Číslo 2
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