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Xiao-Mei Shi

Researcher at University of Toronto

Publications -  15
Citations -  2670

Xiao-Mei Shi is an academic researcher from University of Toronto. The author has contributed to research in topics: Gene & Gene mapping. The author has an hindex of 12, co-authored 15 publications receiving 2557 citations.

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Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene.

TL;DR: Characterization of 5'-flanking genomic regions indicates that the endothelial NO synthase promoter is "TATA-less" and exhibits proximal promoter elements consistent with a constitutively expressed gene that is found in endothelial cells, namely Sp1 and GATA motifs.
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A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11

TL;DR: PCR analysis of somatic cell lines found APJ-related sequences to be only present on chromosome 11, and high-resolution mapping by fluorescence in situ hybridization (FISH) sublocalized APJ on band q12.
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Cloning and Chromosomal Mapping of Three Novel Genes, GPR9, GPR10, and GPR14, Encoding Receptors Related to Interleukin 8, Neuropeptide Y, and Somatostatin Receptors

TL;DR: The polymerase chain reaction and genomic DNA library screening was employed to clone novel human genes, GPR9 and GPR10, and a rat gene, G PR14, which encode G protein-coupled receptors that share the highest identity with human IL-8 receptor type B.
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Cloning of Human Genes Encoding Novel G Protein-Coupled Receptors

TL;DR: The isolation and characterization of several novel human genes encoding G protein-coupled receptors showed identity with a previously characterized cDNA clone from rat and was localized to chromosome 1p35-p36.
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The Cloning and Chromosomal Mapping of Two Novel Human Opioid-Somatostatin-like Receptor Genes, GPR7 and GPR8, Expressed in Discrete Areas of the Brain

TL;DR: Following the cloning of the opioid receptors mu, kappa, and delta, a search for related receptors was conducted using oligonucleotides based on the opioid and also the structurally related somatostatin receptors and isolated fragments of novel G protein-coupled receptor genes named GPR7 and GPR8, which shared 70% identity with each other.