Publication Venue For
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
Effector TH17 Cells Give Rise to Long-Lived TRM Cells that Are Essential for an Immediate Response against Bacterial Infection.
Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions.
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2.
Activated PMN Exosomes: Pathogenic Entities Causing Matrix Destruction and Disease in the Lung.
Erratum: Comprehensive Characterization of Cancer Driver Genes and Mutations (ARTICLE (2018) 173(2) (371–385), (S009286741830237X), (10.1016/j.cell.2018.02.060)).
Erratum: Comprehensive Molecular Characterization of Muscle-Invasive Bladder Cancer (Cell (2017) 171(3) (540–556.e25) (S0092867417310565) (10.1016/j.cell.2017.09.007)).
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.
A Pan-Cancer Analysis of Enhancer Expression in Nearly 9000 Patient Samples.
An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics.
Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer.
Comprehensive Characterization of Cancer Driver Genes and Mutations.
Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation.
Oncogenic Signaling Pathways in The Cancer Genome Atlas.
Pathogenic Germline Variants in 10,389 Adult Cancers.
Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics.
Comprehensive Molecular Characterization of Muscle-Invasive Bladder Cancer.
Development of a Novel Lead that Targets M. tuberculosis Polyketide Synthase 13.
Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma.
An Organismal CNV Mutator Phenotype Restricted to Early Human Development.
Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic Disease.
Loss of IFN-γ Pathway Genes in Tumor Cells as a Mechanism of Resistance to Anti-CTLA-4 Therapy.
Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma.
Evolving New Skeletal Traits by cis-Regulatory Changes in Bone Morphogenetic Proteins.
Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype.
Daughter's Tolerance of Mom Matters in Mate Choice.
Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease.
Neuronal activity promotes glioma growth through neuroligin-3 secretion.
Snap Shot: Sensing and signaling by cilia.
Advancing biological understanding and therapeutics discovery with small-molecule probes.
Integrated Genomic Characterization of Papillary Thyroid Carcinoma.
Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin.
Erratum: The somatic genomic landscape of glioblastoma (Cell (2013) 155 (462-477)).
Ribosomal protein s15 phosphorylation mediates LRRK2 neurodegeneration in parkinson's disease.
Potentiated Hsp104 variants antagonize diverse proteotoxic misfolding events.
Tryptophan biosynthesis protects mycobacteria from CD4 T-Cell-mediated Killing.
The somatic genomic landscape of glioblastoma.
XSpatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
53BP1 mediates productive and mutagenic DNA repair through distinct phosphoprotein interactions.
Dwelling on T cell fate decisions.
Three-dimensional architecture of the rod sensory cilium and its disruption in retinal neurodegeneration.
A validated regulatory network for Th17 cell specification.
A role for small RNAs in DNA double-strand break repair..
Erratum: Generation of isogenic pluripotent stem cells differing exclusively at two early onset parkinson point mutations (Cell (2011) 146 (318-331)).
Generation of isogenic pluripotent stem cells differing exclusively at two early onset parkinson point mutations.
Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies.
Glioma stem cell proliferation and tumor growth are promoted by nitric oxide synthase-2.
Cellular strategies for regulating DNA supercoiling: A single-molecule perspective.
Insulin Receptor Signaling in Osteoblasts Regulates Postnatal Bone Acquisition and Body Composition.
NF1 Is a Tumor Suppressor in Neuroblastoma that Determines Retinoic Acid Response and Disease Outcome.
Natural mutagenesis of human genomes by endogenous retrotransposons.
Role for IGFBP7 in senescence induction by BRAF.
miR-328 Functions as an RNA Decoy to Modulate hnRNP E2 Regulation of mRNA Translation in Leukemic Blasts.
Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance.
PI3 Kinase Signals BCR-Dependent Mature B Cell Survival.
NPR1 in Plant Defense: It's Not over 'til It's Turned over.
Collateral Damage from Antigen Receptor Gene Diversification.
Oncogenic BRAF Induces Senescence and Apoptosis through Pathways Mediated by the Secreted Protein IGFBP7.
Stem Cells on Patrol.
ATM Prevents the Persistence and Propagation of Chromosome Breaks in Lymphocytes.
FOXP3 is an X-linked breast cancer suppressor gene and an important repressor of the HER-2/ErbB2 oncogene..
CHD5 Is a Tumor Suppressor at Human 1p36.
Nef-Mediated Suppression of T Cell Activation Was Lost in a Lentiviral Lineage that Gave Rise to HIV-1.
Cell-surface calreticulin initiates clearance of viable or apoptotic cells through trans-activation of LRP on the phagocyte.
Decoding Dopamine Signaling.
DksA: A critical component of the transcription initiation machinery that potentiates the regulation of rRNA promoters by ppGpp and the initiating NTP.
Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene.
O-GlcNAc modification is an endogenous inhibitor of the proteasome.
Identification of a Wnt/Dvl/β-Catenin → Pitx2 Pathway Mediating Cell-Type-Specific Proliferation during Development.
Drosophila fragile x-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function.
FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium.
Crystal structure of constitutive endothelial nitric oxide synthase: A paradigm for pterin function involving a novel metal center.
Thrombospondin-1 is a major activator of TGF-β1 in vivo.
Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse.
Association of the origin recognition complex with heterochromatin and HP1 in higher eukaryotes.
Targeted disruption of the melanocortin-4 receptor results in obesity in mice.
Identification of an ER retrieval signal in a retroviral glycoprotein.
Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel.
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.
Transferrin receptor internalization sequence YXRF implicates a tight turn as the structural recognition motif for endocytosis.
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation.
Vaccinia virus produces late mRNAs by discontinuous synthesis.
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene.
Rearrangement of antigen receptor genes is defective in mice with severe combined immune deficiency.
Uncoating ATPase is a member of the 70 kilodalton family of stress proteins.
Expression of hemolytically active murine fourth component of complement in transfected L cells.
Four unique genes required for β tubulin expression in vertebrates.
Histone gene clusters of the newt notophthalmus are separated by long tracts of satellite DNA.
Identification of the gene and mRNA for the adenovirus terminal protein precursor.
SV40 gene expression is modulated by the cooperative binding of T antigen to DNA.
Identification and mapping of the transcriptional and translational products of the yeast plasmid, 2μ circle.
A supplementary adenoviral leader sequence and its role in messenger translation.
The spliced structures of adenovirus 2 fiber message and the other late mRNAs.
A map of cytoplasmic RNA transcripts from lytic adenovirus type 2, determined by electron microscopy of RNA:DNA hybrids.
An amazing sequence arrangement at the 5′ ends of adenovirus 2 messenger RNA.
Gene expression in chemically transformed mouse embryo cells: Selective enhancement of the expression of C type RNA tumor virus genes.