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PLOS Genetics - Číslo 5/2010

Research Article

32767

Digital Quantification of Human Eye Color Highlights Genetic Association of Three New Loci

Common Genetic Variants near the Brittle Cornea Syndrome Locus Influence the Blinding Disease Risk Factor Central Corneal Thickness

Age- and Temperature-Dependent Somatic Mutation Accumulation in

Aging and Chronic Sun Exposure Cause Distinct Epigenetic Changes in Human Skin

Transposed Genes in Arabidopsis Are Often Associated with Flanking Repeats

A Survey of Genomic Traces Reveals a Common Sequencing Error, RNA Editing, and DNA Editing

Gene Transposition Causing Natural Variation for Growth in

The Polyproline Site in Hinge 2 Influences the Functional Capacity of Truncated Dystrophins

Epistasis of Transcriptomes Reveals Synergism between Transcriptional Activators Hnf1α and Hnf4α

Integration of Light Signals by the Retinoblastoma Pathway in the Control of S Phase Entry in the Picophytoplanktonic Cell

The Proprotein Convertase Encoded by () Is Required in Corpora Cardiaca Endocrine Cells Producing the Glucose Regulatory Hormone AKH

Sgs1 and Exo1 Redundantly Inhibit Break-Induced Replication and Telomere Addition at Broken Chromosome Ends

A MATE-Family Efflux Pump Rescues the 8-Oxoguanine-Repair-Deficient Mutator Phenotype and Protects Against HO Killing

The Relationship among Gene Expression, the Evolution of Gene Dosage, and the Rate of Protein Evolution

SMA-10/LRIG Is a Conserved Transmembrane Protein that Enhances Bone Morphogenetic Protein Signaling

The Nuclear Receptor DHR3 Modulates dS6 Kinase–Dependent Growth in

Involvement of Global Genome Repair, Transcription Coupled Repair, and Chromatin Remodeling in UV DNA Damage Response Changes during Development

B1 SOX Coordinate Cell Specification with Patterning and Morphogenesis in the Early Zebrafish Embryo

Linkage and Association Mapping of Flowering Time in Nature

Bulk Segregant Analysis by High-Throughput Sequencing Reveals a Novel Xylose Utilization Gene from

Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain

Ablation of Whirlin Long Isoform Disrupts the USH2 Protein Complex and Causes Vision and Hearing Loss

Characterization of Oxidative Guanine Damage and Repair in Mammalian Telomeres

DNA Adenine Methylation Is Required to Replicate Both Chromosomes Once per Cell Cycle

Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies

FACT Prevents the Accumulation of Free Histones Evicted from Transcribed Chromatin and a Subsequent Cell Cycle Delay in G1

GC-Biased Evolution Near Human Accelerated Regions

Liver and Adipose Expression Associated SNPs Are Enriched for Association to Type 2 Diabetes

Myeloid Cell-Restricted Insulin Receptor Deficiency Protects Against Obesity-Induced Inflammation and Systemic Insulin Resistance

The Mating Type Locus () and Sexual Reproduction of : Insights into the Evolution of Sex and Sex-Determining Chromosomal Regions in Fungi

B-Cyclin/CDKs Regulate Mitotic Spindle Assembly by Phosphorylating Kinesins-5 in Budding Yeast

Post-Replication Repair Suppresses Duplication-Mediated Genome Instability

Genome Sequence of the Plant Growth Promoting Endophytic Bacterium sp. 638

Transcription Factors Mat2 and Znf2 Operate Cellular Circuits Orchestrating Opposite- and Same-Sex Mating in

The Use of Orthologous Sequences to Predict the Impact of Amino Acid Substitutions on Protein Function

Mutation in Archain 1, a Subunit of COPI Coatomer Complex, Causes Diluted Coat Color and Purkinje Cell Degeneration

Shelterin-Like Proteins and Yku Inhibit Nucleolytic Processing of Telomeres

Affecting Function Causes a Dilated Heart in Adult

Manipulation of Behavioral Decline in with the Rag GTPase

Interview

32767

All About Mitochondrial Eve: An Interview with Rebecca Cann

PLOS Genetics

2010 Číslo 5

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