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PLOS Genetics - Číslo 10/2011

Perspective

32767

Transcriptional Robustness Complements Nonsense-Mediated Decay in Humans

An Adaptive Allelic Series Featuring Complex Gene Rearrangements

Research Article

32767

Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry

Genetic Determinants of Serum Testosterone Concentrations in Men

A One Base Pair Deletion in the Canine Gene Causes Exon Skipping and Late-Onset Neuronal Ceroid Lipofuscinosis in the Tibetan Terrier

Three Structure-Selective Endonucleases Are Essential in the Absence of BLM Helicase in

Identification of Widespread Ultra-Edited Human RNAs

Multiple Wnts Redundantly Control Polarity Orientation in Epithelial Stem Cells

The Bicoid Stability Factor Controls Polyadenylation and Expression of Specific Mitochondrial mRNAs in

Transcriptome-Wide Binding Sites for Components of the Non-Poly(A) Termination Pathway: Nrd1, Nab3, and Sen1

Macroautophagy Is Regulated by the UPR–Mediator CHOP and Accentuates the Phenotype of SBMA Mice

Genetic Rearrangements Can Modify Chromatin Features at Epialleles

Novel Function of as a Gap Gene during Spider Segmentation

A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

Comparative Genomic Analysis of Human Fungal Pathogens Causing Paracoccidioidomycosis

Genetic Diversity in Cytokines Associated with Immune Variation and Resistance to Multiple Pathogens in a Natural Rodent Population

Mutator Suppression and Escape from Replication Error–Induced Extinction in Yeast

Dynamic Replacement of Histone H3 Variants Reprograms Epigenetic Marks in Early Mouse Embryos

A Barcode Screen for Epigenetic Regulators Reveals a Role for the NuB4/HAT-B Histone Acetyltransferase Complex in Histone Turnover

HIF–VEGF Pathways Are Critical for Chronic Otitis Media in and Mouse Mutants

A Conserved Developmental Patterning Network Produces Quantitatively Different Output in Multiple Species of Drosophila

Role of Exonic Variation in Chemokine Receptor Genes on AIDS: Association with Pneumocystis Pneumonia

Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases

Von Hippel-Lindau () Inactivation in Sporadic Clear Cell Renal Cancer: Associations with Germline Polymorphisms and Etiologic Risk Factors

A Systems Biology Approach Reveals the Role of a Novel Methyltransferase in Response to Chemical Stress and Lipid Homeostasis

Identification of Genomic Regions Associated with Phenotypic Variation between Dog Breeds using Selection Mapping

Global Mapping of Cell Type–Specific Open Chromatin by FAIRE-seq Reveals the Regulatory Role of the NFI Family in Adipocyte Differentiation

Natural Selection Affects Multiple Aspects of Genetic Variation at Putatively Neutral Sites across the Human Genome

MicroRNA Expression and Regulation in Human, Chimpanzee, and Macaque Brains

Feed-Forward Microprocessing and Splicing Activities at a MicroRNA–Containing Intron

Developmental Stability: A Major Role for in

A Phenomics-Based Strategy Identifies Loci on , , and Associated with Metabolic Syndrome Phenotype Domains

Association of , , , , and with Systemic Lupus Erythematosus

Small RNAs Prevent Transcription-Coupled Loss of Histone H3 Lysine 9 Methylation in

Successive Increases in the Resistance of to Viral Infection through a Transposon Insertion Followed by a Duplication

Mutations in a Guanylate Cyclase GCY-35/GCY-36 Modify Bardet-Biedl Syndrome–Associated Phenotypes in

The Glycobiome Reveals Mechanisms of Pentose and Hexose Co-Utilization in Bacteria

Insights into Hox Protein Function from a Large Scale Combinatorial Analysis of Protein Domains

Mutations Cause Seckel and Jawad Syndromes

Zelda Binding in the Early Embryo Marks Regions Subsequently Activated at the Maternal-to-Zygotic Transition

Temporal Coordination of Gene Networks by Zelda in the Early Embryo

Genetic Interaction between MTMR2 and FIG4 Phospholipid Phosphatases Involved in Charcot-Marie-Tooth Neuropathies

Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration

Transforming Growth Factor β Receptor Type 1 Is Essential for Female Reproductive Tract Integrity and Function

Positional Cloning of a Type 2 Diabetes Quantitative Trait Locus; , a Negative Regulator of Insulin Secretion

PLOS Genetics

2011 Číslo 10

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