PLOS Genetics - Číslo 10/2012

Perspective

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

Interview

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It Was Heaven: An Interview with Evelyn Witkin

Research Article

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The Germline Genome Provides a Niche for Intragenic Parasitic DNA: Evolutionary Dynamics of Internal Eliminated Sequences
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Maize Is Required for Maintaining Silencing Associated with Paramutation at the and Loci
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Distinguishing between Selective Sweeps from Standing Variation and from a Mutation
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Cytokinesis-Based Constraints on Polarized Cell Growth in Fission Yeast
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Deposition of Histone Variant H2A.Z within Gene Bodies Regulates Responsive Genes
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Functional Antagonism between Sas3 and Gcn5 Acetyltransferases and ISWI Chromatin Remodelers
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The SET-Domain Protein SUVR5 Mediates H3K9me2 Deposition and Silencing at Stimulus Response Genes in a DNA Methylation–Independent Manner
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Morphogenesis and Cell Fate Determination within the Adaxial Cell Equivalence Group of the Zebrafish Myotome
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Muscle-Specific Splicing Factors ASD-2 and SUP-12 Cooperatively Switch Alternative Pre-mRNA Processing Patterns of the ADF/Cofilin Gene in
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Increasing Signal Specificity of the TOL Network of mt-2 by Rewiring the Connectivity of the Master Regulator XylR
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Deep Genome-Wide Measurement of Meiotic Gene Conversion Using Tetrad Analysis in
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Use of Pleiotropy to Model Genetic Interactions in a Population
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RAB-Like 2 Has an Essential Role in Male Fertility, Sperm Intra-Flagellar Transport, and Tail Assembly
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Variants Affecting Exon Skipping Contribute to Complex Traits
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Topoisomerase II– and Condensin-Dependent Breakage of -Sensitive Fragile Sites Occurs Independently of Spindle Tension, Anaphase, or Cytokinesis
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Comparison of Family History and SNPs for Predicting Risk of Complex Disease
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Recovery of Arrested Replication Forks by Homologous Recombination Is Error-Prone
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A Mutation in the Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse
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Mismatch Repair Balances Leading and Lagging Strand DNA Replication Fidelity
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Specific Missense Alleles of the Arabidopsis Jasmonic Acid Co-Receptor COI1 Regulate Innate Immune Receptor Accumulation and Function
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Calpain-5 Mutations Cause Autoimmune Uveitis, Retinal Neovascularization, and Photoreceptor Degeneration
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A Likelihood-Based Framework for Variant Calling and Mutation Detection in Families
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Cofilin-1: A Modulator of Anxiety in Mice
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The Date of Interbreeding between Neandertals and Modern Humans
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Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development
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Viral Evasion of a Bacterial Suicide System by RNA–Based Molecular Mimicry Enables Infectious Altruism
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Phosphatase-Dead Myotubularin Ameliorates X-Linked Centronuclear Myopathy Phenotypes in Mice
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Full-Length Synaptonemal Complex Grows Continuously during Meiotic Prophase in Budding Yeast
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MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells
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The Contribution of RNA Decay Quantitative Trait Loci to Inter-Individual Variation in Steady-State Gene Expression Levels
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Mutation and Fetal Ethanol Exposure Synergize to Produce Midline Signaling Defects and Holoprosencephaly Spectrum Disorders in Mice
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New Partners in Regulation of Gene Expression: The Enhancer of Trithorax and Polycomb Corto Interacts with Methylated Ribosomal Protein L12 Its Chromodomain
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Mining the Unknown: A Systems Approach to Metabolite Identification Combining Genetic and Metabolic Information
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Mutations in (Hhat) Perturb Hedgehog Signaling, Resulting in Severe Acrania-Holoprosencephaly-Agnathia Craniofacial Defects
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The Many Landscapes of Recombination in
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Faster-X Evolution of Gene Expression in
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Loss of Slc4a1b Chloride/Bicarbonate Exchanger Function Protects Mechanosensory Hair Cells from Aminoglycoside Damage in the Zebrafish Mutant
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Regulation of ATG4B Stability by RNF5 Limits Basal Levels of Autophagy and Influences Susceptibility to Bacterial Infection
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and the BTB Adaptor Are Key Regulators of Sleep Homeostasis and a Dopamine Arousal Pathway in Drosophila
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Comparative Genomics Suggests an Independent Origin of Cytoplasmic Incompatibility in

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