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PLOS Genetics - Číslo 10/2012

Perspective

32767

Classical Genetics Meets Next-Generation Sequencing: Uncovering a Genome-Wide Recombination Map in

Interview

32767

It Was Heaven: An Interview with Evelyn Witkin

Research Article

32767

The Germline Genome Provides a Niche for Intragenic Parasitic DNA: Evolutionary Dynamics of Internal Eliminated Sequences

Calpain-5 Mutations Cause Autoimmune Uveitis, Retinal Neovascularization, and Photoreceptor Degeneration

Cofilin-1: A Modulator of Anxiety in Mice

The Date of Interbreeding between Neandertals and Modern Humans

Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development

Viral Evasion of a Bacterial Suicide System by RNA–Based Molecular Mimicry Enables Infectious Altruism

Phosphatase-Dead Myotubularin Ameliorates X-Linked Centronuclear Myopathy Phenotypes in Mice

Full-Length Synaptonemal Complex Grows Continuously during Meiotic Prophase in Budding Yeast

MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells

A Likelihood-Based Framework for Variant Calling and Mutation Detection in Families

The Contribution of RNA Decay Quantitative Trait Loci to Inter-Individual Variation in Steady-State Gene Expression Levels

New Partners in Regulation of Gene Expression: The Enhancer of Trithorax and Polycomb Corto Interacts with Methylated Ribosomal Protein L12 Its Chromodomain

Mining the Unknown: A Systems Approach to Metabolite Identification Combining Genetic and Metabolic Information

Mutations in (Hhat) Perturb Hedgehog Signaling, Resulting in Severe Acrania-Holoprosencephaly-Agnathia Craniofacial Defects

The Many Landscapes of Recombination in

Faster-X Evolution of Gene Expression in

Loss of Slc4a1b Chloride/Bicarbonate Exchanger Function Protects Mechanosensory Hair Cells from Aminoglycoside Damage in the Zebrafish Mutant

Regulation of ATG4B Stability by RNF5 Limits Basal Levels of Autophagy and Influences Susceptibility to Bacterial Infection

and the BTB Adaptor Are Key Regulators of Sleep Homeostasis and a Dopamine Arousal Pathway in Drosophila

Mutation and Fetal Ethanol Exposure Synergize to Produce Midline Signaling Defects and Holoprosencephaly Spectrum Disorders in Mice

Specific Missense Alleles of the Arabidopsis Jasmonic Acid Co-Receptor COI1 Regulate Innate Immune Receptor Accumulation and Function

Deep Genome-Wide Measurement of Meiotic Gene Conversion Using Tetrad Analysis in

Mismatch Repair Balances Leading and Lagging Strand DNA Replication Fidelity

Distinguishing between Selective Sweeps from Standing Variation and from a Mutation

Cytokinesis-Based Constraints on Polarized Cell Growth in Fission Yeast

Deposition of Histone Variant H2A.Z within Gene Bodies Regulates Responsive Genes

Functional Antagonism between Sas3 and Gcn5 Acetyltransferases and ISWI Chromatin Remodelers

The SET-Domain Protein SUVR5 Mediates H3K9me2 Deposition and Silencing at Stimulus Response Genes in a DNA Methylation–Independent Manner

Morphogenesis and Cell Fate Determination within the Adaxial Cell Equivalence Group of the Zebrafish Myotome

Muscle-Specific Splicing Factors ASD-2 and SUP-12 Cooperatively Switch Alternative Pre-mRNA Processing Patterns of the ADF/Cofilin Gene in

Maize Is Required for Maintaining Silencing Associated with Paramutation at the and Loci

Increasing Signal Specificity of the TOL Network of mt-2 by Rewiring the Connectivity of the Master Regulator XylR

Use of Pleiotropy to Model Genetic Interactions in a Population

RAB-Like 2 Has an Essential Role in Male Fertility, Sperm Intra-Flagellar Transport, and Tail Assembly

Variants Affecting Exon Skipping Contribute to Complex Traits

Topoisomerase II– and Condensin-Dependent Breakage of -Sensitive Fragile Sites Occurs Independently of Spindle Tension, Anaphase, or Cytokinesis

Comparison of Family History and SNPs for Predicting Risk of Complex Disease

Recovery of Arrested Replication Forks by Homologous Recombination Is Error-Prone

A Mutation in the Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse

Comparative Genomics Suggests an Independent Origin of Cytoplasmic Incompatibility in

PLOS Genetics

2012 Číslo 10

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