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PLOS Genetics - Číslo 10/2010

Research Article

32767

Common Genetic Variants and Modification of Penetrance of -Associated Breast Cancer

Genome-Wide Identification of Targets and Function of Individual MicroRNAs in Mouse Embryonic Stem Cells

Allele-Specific Down-Regulation of Expression Induced by Retinoids Contributes to Climate Adaptations

The Meiotic Recombination Checkpoint Suppresses NHK-1 Kinase to Prevent Reorganisation of the Oocyte Nucleus in

Actin Depolymerizing Factors Cofilin1 and Destrin Are Required for Ureteric Bud Branching Morphogenesis

DSIF and RNA Polymerase II CTD Phosphorylation Coordinate the Recruitment of Rpd3S to Actively Transcribed Genes

Continuous Requirement for the Clr4 Complex But Not RNAi for Centromeric Heterochromatin Assembly in Fission Yeast Harboring a Disrupted RITS Complex

Genome-Wide Association Study of Blood Pressure Extremes Identifies Variant near Associated with Hypertension

The Cytosine Methyltransferase DRM2 Requires Intact UBA Domains and a Catalytically Mutated Paralog DRM3 during RNA–Directed DNA Methylation in

β-Actin and γ-Actin Are Each Dispensable for Auditory Hair Cell Development But Required for Stereocilia Maintenance

Genetic Association Study Identifies as a Risk Gene for Idiopathic Dilated Cardiomyopathy

Evidence for a Xer/ System for Chromosome Resolution in Archaea

Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation

Lifespan Extension by Preserving Proliferative Homeostasis in

Ancient and Recent Adaptive Evolution of Primate Non-Homologous End Joining Genes

Loss of the p53/p63 Regulated Desmosomal Protein Perp Promotes Tumorigenesis

Altering a Histone H3K4 Methylation Pathway in Glomerular Podocytes Promotes a Chronic Disease Phenotype

Characterization of LINE-1 Ribonucleoprotein Particles

Conserved Genes Act as Modifiers of Invertebrate SMN Loss of Function Defects

Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier

Tight Regulation of the Gene of the KplE1 Prophage: A New Paradigm for Integrase Gene Regulation

Conjugative DNA Transfer Induces the Bacterial SOS Response and Promotes Antibiotic Resistance Development through Integron Activation

Nasty Viruses, Costly Plasmids, Population Dynamics, and the Conditions for Establishing and Maintaining CRISPR-Mediated Adaptive Immunity in Bacteria

Stress-Induced Activation of Heterochromatic Transcription

H3K27me3 Profiling of the Endosperm Implies Exclusion of Polycomb Group Protein Targeting by DNA Methylation

Simultaneous Disruption of Two DNA Polymerases, Polη and Polζ, in Avian DT40 Cells Unmasks the Role of Polη in Cellular Response to Various DNA Lesions

Characterising and Predicting Haploinsufficiency in the Human Genome

Dual Functions of ASCIZ in the DNA Base Damage Response and Pulmonary Organogenesis

Pervasive Cryptic Epistasis in Molecular Evolution

Transition from Positive to Neutral in Mutation Fixation along with Continuing Rising Fitness in Thermal Adaptive Evolution

Comprehensive Analysis Reveals Dynamic and Evolutionary Plasticity of Rab GTPases and Membrane Traffic in

Regulates Tissue-Specific Mitochondrial DNA Segregation

Role for the Mammalian Swi5-Sfr1 Complex in DNA Strand Break Repair through Homologous Recombination

Perspective

32767

FSHD: A Repeat Contraction Disease Finally Ready to Expand (Our Understanding of Its Pathogenesis)

PLOS Genetics

2010 Číslo 10

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