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plos genetics
  
سال:2014 - دوره:10 - شماره:5
  
 
A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation
  
 
A Genome-Wide Assessment of the Role of Untagged Copy Number Variants in Type 1 Diabetes
  
 
A HECT Ubiquitin-Protein Ligase as a Novel Candidate Gene for Altered Quinine and Quinidine Responses in Plasmodium falciparum
  
 
A Lack of Parasitic Reduction in the Obligate Parasitic Green Alga Helicosporidium
  
 
A Mutation in the FAM83G Gene in Dogs with Hereditary Footpad Hyperkeratosis (HFH)
  
 
A Novel C2H2 Transcription Factor that Regulates gliA Expression Interdependently with GliZ in Aspergillus fumigatus
  
 
Activating Transcription Factor 6 Is Necessary and Sufficient for Alcoholic Fatty Liver Disease in Zebrafish
  
 
Allele-Specific Genome-wide Profiling in Human Primary Erythroblasts Reveal Replication Program Organization
  
 
Allelic Expression of Deleterious Protein-Coding Variants across Human Tissues
  
 
An In Vivo EGF Receptor Localization Screen in C. elegans Identifies the Ezrin Homolog ERM-1 as a Temporal Regulator of Signaling
  
 
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
  
 
Biased,Non-equivalent Gene-Proximal and -Distal Binding Motifs of Orphan Nuclear Receptor TR4 in Primary Human Erythroid Cells
  
 
Copy Number Variation Is a Fundamental Aspect of the Placental Genome
  
 
Discovery and Functional Annotation of SIX6 Variants in Primary Open-Angle Glaucoma
  
 
Drosha Promotes Splicing of a Pre-microRNA-like Alternative Exon
  
 
Drosophila melanogaster Hox Transcription Factors Access the RNA Polymerase II Machinery through Direct Homeodomain Binding to a Conserved Motif of Mediator Subunit Med19
  
 
EDR1 Physically Interacts with MKK4/MKK5 and Negatively Regulates a MAP Kinase Cascade to Modulate Plant Innate Immunity
  
 
Enhanced Interaction between Pseudokinase and Kinase Domains in Gcn2 stimulates eIF2α Phosphorylation in Starved Cells
  
 
Epistatically Interacting Substitutions Are Enriched during Adaptive Protein Evolution
  
 
Extensive Diversity of Prion Strains Is Defined by Differential Chaperone Interactions and Distinct Amyloidogenic Regions
  
 
Fine Tuning of the UPR by the Ubiquitin Ligases Siah1/2
  
 
GOLPH3 Is Essential for Contractile Ring Formation and Rab11 Localization to the Cleavage Site during Cytokinesis in Drosophila melanogaster
  
 
Genes That Bias Mendelian Segregation
  
 
Genetic Dissection of the Drosophila melanogaster Female Head Transcriptome Reveals Widespread Allelic Heterogeneity
  
 
Genetic Interactions Involving Five or More Genes Contribute to a Complex Trait in Yeast
  
 
Genome Sequencing and Comparative Genomics of the Broad Host-Range Pathogen Rhizoctonia solani AG8
  
 
Genome-Wide Inference of Ancestral Recombination Graphs
  
 
Genome-Wide Nucleosome Positioning Is Orchestrated by Genomic Regions Associated with DNase I Hypersensitivity in Rice
  
 
G×G×E for Lifespan in Drosophila: Mitochondrial,Nuclear,and Dietary Interactions that Modify Longevity
  
 
Heritable Transmission of Stress Resistance by High Dietary Glucose in Caenorhabditis elegans
  
 
Heterogeneity in the Frequency and Characteristics of Homologous Recombination in Pneumococcal Evolution
  
 
Hyperactivated Wnt Signaling Induces Synthetic Lethal Interaction with Rb Inactivation by Elevating TORC1 Activities
  
 
Insights into the Genetic Structure and Diversity of 38 South Asian Indians from Deep Whole-Genome Sequencing
  
 
Intron Retention in the 5′UTR of the Novel ZIF2 Transporter Enhances Translation to Promote Zinc Tolerance in Arabidopsis
  
 
Lifespan Extension by Methionine Restriction Requires Autophagy-Dependent Vacuolar Acidification
  
 
Loss of Function Mutation in the Palmitoyl-Transferase HHAT Leads to Syndromic 46,XY Disorder of Sex Development by Impeding Hedgehog Protein Palmitoylation and Signaling
  
 
Meiotic Drive Impacts Expression and Evolution of X-Linked Genes in Stalk-Eyed Flies
  
 
Mlh2 Is an Accessory Factor for DNA Mismatch Repair in Saccharomyces cerevisiae
  
 
More of a Good Thing or Less of a Bad Thing: Gene Copy Number Variation in Polyploid Cells of the Placenta
  
 
Mosaic Epigenetic Dysregulation of Ectodermal Cells in Autism Spectrum Disorder
  
 
Mutations in Four Glycosyl Hydrolases Reveal a Highly Coordinated Pathway for Rhodopsin Biosynthesis and N-Glycan Trimming in Drosophila melanogaster
  
 
Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth
  
 
Null Mutation in PGAP1 Impairing Gpi-Anchor Maturation in Patients with Intellectual Disability and Encephalopathy
  
 
Octopamine Neuromodulation Regulates Gr32a-Linked Aggression and Courtship Pathways in Drosophila Males
  
 
PAX6 Regulates Melanogenesis in the Retinal Pigmented Epithelium through Feed-Forward Regulatory Interactions with MITF
  
 
PINK1-Parkin Pathway Activity Is Regulated by Degradation of PINK1 in the Mitochondrial Matrix
  
 
Paternal Poly (ADP-ribose) Metabolism Modulates Retention of Inheritable Sperm Histones and Early Embryonic Gene Expression
  
 
Phosphorylation Modulates Clearance of Alpha-Synuclein Inclusions in a Yeast Model of Parkinson's Disease
  
 
Phosphorylation of a WRKY Transcription Factor by MAPKs Is Required for Pollen Development and Function in Arabidopsis
  
 
Population Genomic Analysis of Ancient and Modern Genomes Yields New Insights into the Genetic Ancestry of the Tyrolean Iceman and the Genetic Structure of Europe
  
 
Predicting the Minimal Translation Apparatus: Lessons from the Reductive Evolution of Mollicutes
  
 
R-loops Associated with Triplet Repeat Expansions Promote Gene Silencing in Friedreich Ataxia and Fragile X Syndrome
  
 
RPM-1 Uses Both Ubiquitin Ligase and Phosphatase-Based Mechanisms to Regulate DLK-1 during Neuronal Development
  
 
Rapid Evolution of PARP Genes Suggests a Broad Role for ADP-Ribosylation in Host-Virus Conflicts
  
 
Ras-Mediated Deregulation of the Circadian Clock in Cancer
  
 
Recent Mitochondrial DNA Mutations Increase the Risk of Developing Common Late-Onset Human Diseases
  
 
Retinoic Acid-Related Orphan Receptor γ (RORγ): A Novel Participant in the Diurnal Regulation of Hepatic Gluconeogenesis and Insulin Sensitivity
  
 
Retinoid-X-Receptors (α/β) in Melanocytes Modulate Innate Immune Responses and Differentially Regulate Cell Survival following UV Irradiation
  
 
Revertant Mutation Releases Confined Lethal Mutation,Opening Pandora's Box: A Novel Genetic Pathogenesis
  
 
Ribosomal Protein Mutations Induce Autophagy through S6 Kinase Inhibition of the Insulin Pathway
  
 
SHP2 Regulates Chondrocyte Terminal Differentiation,Growth Plate Architecture and Skeletal Cell Fates
  
 
Scribble Modulates the MAPK/Fra1 Pathway to Disrupt Luminal and Ductal Integrity and Suppress Tumour Formation in the Mammary Gland
  
 
Selectivity in Genetic Association with Sub-classified Migraine in Women
  
 
Single Nucleotide Variants in Transcription Factors Associate More Tightly with Phenotype than with Gene Expression
  
 
Six Homeoproteins and a Iinc-RNA at the Fast MYH Locus Lock Fast Myofiber Terminal Phenotype
  
 
Spermatid Cyst Polarization in Drosophila Depends upon apkc and the CPEB Family Translational Regulator orb2
  
 
The Case for Junk DNA
  
 
The Impact of Population Demography and Selection on the Genetic Architecture of Complex Traits
  
 
The Impairment of MAGMAS Function in Human Is Responsible for a Severe Skeletal Dysplasia
  
 
The Proper Splicing of RNAi Factors Is Critical for Pericentric Heterochromatin Assembly in Fission Yeast
  
 
The Spatiotemporal Program of DNA Replication Is Associated with Specific Combinations of Chromatin Marks in Human Cells
  
 
Whole Exome Re-Sequencing Implicates CCDC38 and Cilia Structure and Function in Resistance to Smoking Related Airflow Obstruction
  
 
dGTP Starvation in Escherichia coli Provides New Insights into the Thymineless-Death Phenomenon
  
 
p53 Requires the Stress Sensor USF1 to Direct Appropriate Cell Fate Decision
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