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PLOS Genetics - Číslo 7/2011

Research Article

32767

Gene-Based Tests of Association

Variants in and Underlie Natural Variation in Translation Termination Efficiency in

SHH1, a Homeodomain Protein Required for DNA Methylation, As Well As RDR2, RDM4, and Chromatin Remodeling Factors, Associate with RNA Polymerase IV

Genome-Wide Association Study Identifies as a Susceptibility Gene for Pediatric Asthma in Asian Populations

Pervasive Sign Epistasis between Conjugative Plasmids and Drug-Resistance Chromosomal Mutations

Genetic Anticipation Is Associated with Telomere Shortening in Hereditary Breast Cancer

Identification of a Mutation Associated with Fatal Foal Immunodeficiency Syndrome in the Fell and Dales Pony

Stress-Induced PARP Activation Mediates Recruitment of Mi-2 to Promote Heat Shock Gene Expression

An Epigenetic Switch Involving Overlapping Fur and DNA Methylation Optimizes Expression of a Type VI Secretion Gene Cluster

Recombination and Population Structure in

A Rice Plastidial Nucleotide Sugar Epimerase Is Involved in Galactolipid Biosynthesis and Improves Photosynthetic Efficiency

A Role for Phosphatidic Acid in the Formation of “Supersized” Lipid Droplets

Colon Stem Cell and Crypt Dynamics Exposed by Cell Lineage Reconstruction

Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

Interactions between Glucocorticoid Treatment and Cis-Regulatory Polymorphisms Contribute to Cellular Response Phenotypes

Translation Reinitiation Relies on the Interaction between eIF3a/TIF32 and Progressively Folded -Acting mRNA Elements Preceding Short uORFs

DAF-12 Regulates a Connected Network of Genes to Ensure Robust Developmental Decisions

Adult Circadian Behavior in Requires Developmental Expression of , But Not

Histone Crosstalk Directed by H2B Ubiquitination Is Required for Chromatin Boundary Integrity

Proteins in the Nutrient-Sensing and DNA Damage Checkpoint Pathways Cooperate to Restrain Mitotic Progression following DNA Damage

Complex Evolutionary Events at a Tandem Cluster of Genes Resulting in a Single-Locus Genetic Incompatibility

() and Its Regulated Homeodomain Gene Mediate Abscisic Acid Response in

A Functional Variant at a Prostate Cancer Predisposition Locus at 8q24 Is Associated with Expression

LGI2 Truncation Causes a Remitting Focal Epilepsy in Dogs

Adaptations to Endosymbiosis in a Cnidarian-Dinoflagellate Association: Differential Gene Expression and Specific Gene Duplications

The Translation Initiation Factor eIF4E Regulates the Sex-Specific Expression of the Master Switch Gene in

Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome

Replication and Explorations of High-Order Epistasis Using a Large Advanced Intercross Line Pedigree

Mechanisms of Chromosome Number Evolution in Yeast

Regulatory Cross-Talk Links Chromosome II Replication and Segregation

Ancestral Genes Can Control the Ability of Horizontally Acquired Loci to Confer New Traits

Expression of Tumor Suppressor in Spermatogonia Facilitates Meiotic Progression in Male Germ Cells

Rare and Common Regulatory Variation in Population-Scale Sequenced Human Genomes

The Epistatic Relationship between BRCA2 and the Other RAD51 Mediators in Homologous Recombination

Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy

NatF Contributes to an Evolutionary Shift in Protein N-Terminal Acetylation and Is Important for Normal Chromosome Segregation

Araucan and Caupolican Integrate Intrinsic and Signalling Inputs for the Acquisition by Muscle Progenitors of the Lateral Transverse Fate

Pathologic and Phenotypic Alterations in a Mouse Expressing a Connexin47 Missense Mutation That Causes Pelizaeus-Merzbacher–Like Disease in Humans

Recombinant Inbred Line Genotypes Reveal Inter-Strain Incompatibility and the Evolution of Recombination

Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

Genetic Loci Associated with Plasma Phospholipid n-3 Fatty Acids: A Meta-Analysis of Genome-Wide Association Studies from the CHARGE Consortium

Fine Mapping of Five Loci Associated with Low-Density Lipoprotein Cholesterol Detects Variants That Double the Explained Heritability

CHD1 Remodels Chromatin and Influences Transient DNA Methylation at the Clock Gene

Nonlinear Fitness Landscape of a Molecular Pathway

Genome-Wide Scan Identifies , , and as Novel Risk Loci for Systemic Sclerosis

Quantitative and Qualitative Stem Rust Resistance Factors in Barley Are Associated with Transcriptional Suppression of Defense Regulons

A Systematic Screen for Tube Morphogenesis and Branching Genes in the Tracheal System

Perspective

32767

Epistatic Relationships in the BRCA1-BRCA2 Pathway

Review

32767

The Demoiselle of X-Inactivation: 50 Years Old and As Trendy and Mesmerising As Ever

Somatic Genetics Empowers the Mouse for Modeling and Interrogating Developmental and Disease Processes

PLOS Genetics

2011 Číslo 7

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