subject area of
- A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy Journal Article
- A functional mutation in the terminal exon of elastin in severe, early-onset chronic obstructive pulmonary disease Journal Article
- A murine model for hypertrophic cardiomyopathy Journal Article
- A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease Journal Article
- A preliminary examination of how serotonergic polymorphisms influence brain response following an adolescent cannabis intervention Journal Article
- AUTOGENOUS TRANSLATIONAL OPERATOR RECOGNIZED BY BACTERIOPHAGE-T4 DNA-POLYMERASE Journal Article
- Analysis of a Critical Interaction within the Archaeal Box C/D Small Ribonucleoprotein Complex Journal Article
- Bioinformatics assessment of β-myosin mutations reveals myosin's high sensitivity to mutations Journal Article
- Characterization of protein-protein interactions critical for poliovirus replication: Analysis of 3AB and VPg binding to the RNA-dependent RNA polymerase Journal Article
- Comparison of methods for estimating the nucleotide substitution matrix Journal Article
- Conserved RNA-binding specificity of polycomb repressive complex 2 is achieved by dispersed amino acid patches in EZH2 Journal Article
- Coordinated Action of Nap1 and RSC in Disassembly of Tandem Nucleosomes Journal Article
- DIFFERENTIAL EFFECTIVENESS OF YEAST CYTOCHROME-C-OXIDASE SUBUNIT-V GENES RESULTS FROM DIFFERENCES IN EXPRESSION NOT FUNCTION Journal Article
- Dopamine transporter polymorphism associated with externalizing behavior problems in children Journal Article
- Extracellular-Regulated Kinase 2 Is Activated by the Enhancement of Hinge Flexibility Journal Article
- FUNCTIONAL-ANALYSIS OF HUMAN CARDIAC GAP JUNCTION CHANNEL MUTANTS Journal Article
- Family-based association test of the 5HTTLPR and aggressive behavior in a general population sample of children Journal Article
- Genetic dissection of quantitative trait locus for ethanol sensitivity in long- and short-sleep mice Journal Article
- Genome-wide mapping of mutations at single-nucleotide resolution for protein, metabolic and genome engineering Journal Article
- Human gamma-aminobutyric acid A receptor alpha 2 gene moderates the acute effects of alcohol and brain mRNA expression Journal Article
- INCREASED FREQUENCY OF DELETIONS IN THE MITOCHONDRIAL GENOME WITH AGE OF CAENORHABDITIS-ELEGANS Journal Article
- Identification of the beta-binding domain of the alpha subunit of Escherichia coli polymerase III holoenzyme. Journal Article
- Individual and Additive Effects of the CNR1 and FAAH Genes on Brain Response to Marijuana Cues Journal Article
- Localization of the active site of the alpha subunit of the Escherichia coli DNA polymerase III holoenzyme. Journal Article
- MANY OF THE CONSERVED NUCLEOTIDES OF TRNA(PHE) ARE NOT ESSENTIAL FOR TERNARY COMPLEX-FORMATION AND PEPTIDE ELONGATION Journal Article
- Multiple C-Terminal Tails within a Single E. coli SSB Homotetramer Coordinate DNA Replication and Repair Journal Article
- Novel FGF8 Mutations Associated with Recessive Holoprosencephaly, Craniofacial Defects, and Hypothalamo-Pituitary Dysfunction Journal Article
- Number of Nevi and early-life ambient UV exposure are associated with BRAF-mutant melanoma Journal Article
- Poly(ADP-ribose) polymerase 1 searches DNA via a 'monkey bar' mechanism Journal Article
- RECOGNITION NUCLEOTIDES FOR HUMAN PHENYLALANYL-TRANSFER RNA-SYNTHETASE Journal Article
- Reading disability and chromosome 6p21.3: Evaluation of MOG as a candidate gene Journal Article
- Regulatory approved monoclonal antibodies contain framework mutations predicted from human antibody repertoires Journal Article
- STRUCTURAL-ANALYSIS OF 2 GENES ENCODING DIVERGENT FORMS OF YEAST CYTOCHROME-C-OXIDASE SUBUNIT-V Journal Article
- Single gold-bridged nanoprobes for identification of single point DNA mutations Journal Article
- Telomerase in Bladder Cancer: Back to a Better Future? Journal Article
- The RNA-binding protein Tsunagi interacts with Mago Nashi to establish polarity and localize oskar mRNA during Drosophila oogenesis Journal Article
- The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease Journal Article
- ZINC(II) AND THE SINGLE-STRANDED-DNA BINDING-PROTEIN OF BACTERIOPHAGE-T4 Journal Article