| Update of human and mouse forkhead box (FOX) gene families |
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| The clinical application of UGT1A1pharmacogenetic testing: Gene-environment interactions |
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| Update of human and mouse matrix metalloproteinase families |
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| Hyperferritinaemia-cataract syndrome: Worldwide mutations and phenotype of an increasingly diagnosed genetic disorder |
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| KinSNP software for homozygosity mapping of disease genes using SNP microarrays |
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| ArrayTrack: a free FDA bioinformatics tool to support emerging biomedical research -- an update |
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| The Machinery of Life: David S. Goodsell 2nd edn., 2009 Springer-Verlag, London |
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| Intronic polymorphisms of cytochromes P450 |
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| An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) gene |
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| The clinical pharmacogeneticist: An emerging regulatory scientist at the US Food and Drug Administration |
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| A useful tool for drug interaction evaluation: The University of Washington Metabolism and Transport Drug Interaction Database |
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| A survey of current software for network analysis in molecular biology |
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| ETHNOS: A versatile electronic tool for the development and curation of national genetic databases |
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| Combination of 16S rRNA variable regions provides a detailed analysis of bacterial community dynamics in the lungs of cystic fibrosis patients |
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| General considerations for integrating pharmacogenomics into mainstream medical practice |
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| The Human Cytochrome P450 (CYP) Allele Nomenclature website: a peer-reviewed database of CYP variants and their associated effects |
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| Evolutionary divergence and functions of the human acyl-CoA thioesterase gene (ACOT) family |
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| Highlights of the 'Gene Nomenclature Across Species' Meeting |
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| Krüppel-like factors: Three fingers in control |
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| Metagenomics: Theory, methods, and applications |
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| Maternal transmission of Alzheimer's disease: Prodromal metabolic phenotype and the search for genes |
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| From DNA to proteins via the ribosome: Structural insights into the workings of the translation machinery |
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| An introduction to effective use of enrichment analysis software |
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| Pharmaceutical biotechnology - concepts and applications |
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| The CATH database |
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| State of the art de novo assembly of human genomes from massively parallel sequencing data |
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| Color Atlas of Pharmacology |
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| Prospects for the automated extraction of mutation data from the scientific literature |
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| What the papers say: Text mining for genomics and systems biology |
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| Functional intronic polymorphisms: Buried treasure awaiting discovery within our genes |
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| Characterisation of a functional intronic polymorphism in the human growth hormone (GHI) gene |
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| Endothelial nitric oxide synthase gene polymorphisms -786T >C and 894G >T in coronary artery bypass graft surgery patients |
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| Gene-environment interaction tests for family studies with quantitative phenotypes: A review and extension to longitudinal measures |
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| The other lives of ribosomal proteins |
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| Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides, as well as in CpG dinucleotides |
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| A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation |
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| Evolutionary divergence and functions of the human interleukin (IL) gene family |
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| Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis |
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African Americans |
| A survey of statistical software for analysing RNA-seq data |
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| Vogel and Motulsky's human genetics--problems and approaches |
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