Výpis čísla časopisu 2/2012 PLOS Genetics

32767

A Strong Deletion Bias in Nonallelic Gene Conversion

Positive Selection for New Disease Mutations in the Human Germline: Evidence from the Heritable Cancer Syndrome Multiple Endocrine Neoplasia Type 2B

Genome-Wide Association Study in East Asians Identifies Novel Susceptibility Loci for Breast Cancer

Mixed Effects Modeling of Proliferation Rates in Cell-Based Models: Consequence for Pharmacogenomics and Cancer

Reduction of NADPH-Oxidase Activity Ameliorates the Cardiovascular Phenotype in a Mouse Model of Williams-Beuren Syndrome

Genome-Wide Association Study Identifies Chromosome 10q24.32 Variants Associated with Arsenic Metabolism and Toxicity Phenotypes in Bangladesh

Structural Basis of Transcriptional Gene Silencing Mediated by MOM1

Genomic Restructuring in the Tasmanian Devil Facial Tumour: Chromosome Painting and Gene Mapping Provide Clues to Evolution of a Transmissible Tumour

Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations

Contrasting Properties of Gene-Specific Regulatory, Coding, and Copy Number Mutations in : Frequency, Effects, and Dominance

The Origin and Nature of Tightly Clustered Deletions in Precursor B-Cell Acute Lymphoblastic Leukemia Support a Model of Multiclonal Evolution

Ultrafast Evolution and Loss of CRISPRs Following a Host Shift in a Novel Wildlife Pathogen,

Phosphorylation of Chromosome Core Components May Serve as Axis Marks for the Status of Chromosomal Events during Mammalian Meiosis

Psoriasis Patients Are Enriched for Genetic Variants That Protect against HIV-1 Disease

A Pathogenic Mechanism in Huntington's Disease Involves Small CAG-Repeated RNAs with Neurotoxic Activity

The Mitochondrial Chaperone Protein TRAP1 Mitigates α-Synuclein Toxicity

Homeobox Genes Critically Regulate Embryo Implantation by Controlling Paracrine Signaling between Uterine Stroma and Epithelium

Developmental Transcriptional Networks Are Required to Maintain Neuronal Subtype Identity in the Mature Nervous System

Down-Regulating Sphingolipid Synthesis Increases Yeast Lifespan

Gene Expression and Stress Response Mediated by the Epigenetic Regulation of a Transposable Element Small RNA

Loss of Tgif Function Causes Holoprosencephaly by Disrupting the Shh Signaling Pathway

Sequestration of Highly Expressed mRNAs in Cytoplasmic Granules, P-Bodies, and Stress Granules Enhances Cell Viability

Discovery of a Modified Tetrapolar Sexual Cycle in and the Evolution of in the Species Complex

The Role of Glypicans in Wnt Inhibitory Factor-1 Activity and the Structural Basis of Wif1's Effects on Wnt and Hedgehog Signaling

Nondisjunction of a Single Chromosome Leads to Breakage and Activation of DNA Damage Checkpoint in G2

A Regulatory Network for Coordinated Flower Maturation

Coexpression Network Analysis in Abdominal and Gluteal Adipose Tissue Reveals Regulatory Genetic Loci for Metabolic Syndrome and Related Phenotypes

The Empirical Power of Rare Variant Association Methods: Results from Sanger Sequencing in 1,998 Individuals

Systematic Detection of Epistatic Interactions Based on Allele Pair Frequencies

Familial Identification: Population Structure and Relationship Distinguishability

Raf1 Is a DCAF for the Rik1 DDB1-Like Protein and Has Separable Roles in siRNA Generation and Chromatin Modification

Loss of Function of the Cik1/Kar3 Motor Complex Results in Chromosomes with Syntelic Attachment That Are Sensed by the Tension Checkpoint

Computational Prediction and Molecular Characterization of an Oomycete Effector and the Cognate Resistance Gene

The Dynamics and Prognostic Potential of DNA Methylation Changes at Stem Cell Gene Loci in Women's Cancer

GTPase Activity and Neuronal Toxicity of Parkinson's Disease–Associated LRRK2 Is Regulated by ArfGAP1

Evaluation of the Role of Functional Constraints on the Integrity of an Ultraconserved Region in the Genus

Neurophysiological Defects and Neuronal Gene Deregulation in Mutants

Genetic and Functional Analyses of Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

Negative Supercoiling Creates Single-Stranded Patches of DNA That Are Substrates for AID–Mediated Mutagenesis

Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution

The Eph Receptor Activates NCK and N-WASP, and Inhibits Ena/VASP to Regulate Growth Cone Dynamics during Axon Guidance

Repression of a Potassium Channel by Nuclear Hormone Receptor and TGF-β Signaling Modulates Insulin Signaling in

The Retrohoming of Linear Group II Intron RNAs in Occurs by Both DNA Ligase 4–Dependent and –Independent Mechanisms

Cell Lineage Analysis of the Mammalian Female Germline

Association of a Functional Variant in the Wnt Co-Receptor with Early Onset Ileal Crohn's Disease

32767

Upsetting the Dogma: Germline Selection in Human Males

Diced Triplets Expose Neurons to RISC

The Williams-Beuren Syndrome—A Window into Genetic Variants Leading to the Development of Cardiovascular Disease

PLOS Genetics - Číslo 2/2012

Research Article

Perspective

PLOS Genetics