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Subject Areas on Research
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2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
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A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes.
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A gene map of the human genome.
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A map of 75 human ribosomal protein genes.
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A physical map of 30,000 human genes.
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A physical map of the human Y chromosome.
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A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequences.
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Alterations in slow-twitch muscle phenotype in transgenic mice overexpressing the Ca2+ buffering protein parvalbumin.
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An STS-based map of the human genome.
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Annotating nonspecific SAGE tags with microarray data.
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Are sequence family variants useful for identifying deletions in the human Y chromosome?
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Assignment of the creatine transporter gene (SLC6A8) to human chromosome Xq28 telomeric to G6PD.
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Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.
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Bacterial artificial chromosome cloning and mapping of a 630-kb human extrachromosomal structure.
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Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses.
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Differential regulation of dopamine D1A receptor responsiveness by various G protein-coupled receptor kinases.
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F-Seq: a feature density estimator for high-throughput sequence tags.
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Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS).
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Genome-wide tagging for everyone.
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Genomic amplification and oncogenic properties of the KCNK9 potassium channel gene.
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Genomic and genetic definition of a functional human centromere.
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High-resolution comparative physical mapping of mouse chromosome 10 in the region of homology with human chromosome 21.
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Identification and mapping of a novel human gene, HRMT1L1, homologous to the rat protein arginine N-methyltransferase 1 (PRMT1) gene.
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Identification of genetic markers to 20 NIDDM candidate genes by radiation hybrid analysis.
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Identification of novel genes preferentially expressed in the retina using a custom human retina cDNA microarray.
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Large-scale identification and analysis of genome-wide single-nucleotide polymorphisms for mapping in Arabidopsis thaliana.
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Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.
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Mapping of transcription start sites in Saccharomyces cerevisiae using 5' SAGE.
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Members of the G protein-coupled receptor kinase family that phosphorylate the beta2-adrenergic receptor facilitate sequestration.
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Monitoring the efficacy of hybrid selection during positional cloning: the search for BRCA1.
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PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis.
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Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellites.
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Phosphorylation of O6-alkylguanine-DNA alkyltransferase: experience with a GST-fusion protein and a new pull-down assay.
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Physical and cDNA mapping in the DBH region of human chromosome 9q34.
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Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
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Report and abstracts of the sixth international workshop on human chromosome 1 mapping 2000. Iowa City, Iowa, USA. 30 September-3 October 2000.
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Rhodopsin maturation antagonized by dominant rhodopsin mutants.
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The alpha-synuclein gene in multiple system atrophy.
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Thrombin primes responsiveness of selective chemoattractant receptors at a site distal to G protein activation.