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Mark A. Bolanowski

Researcher at Howard Hughes Medical Institute

Publications -  5
Citations -  2311

Mark A. Bolanowski is an academic researcher from Howard Hughes Medical Institute. The author has contributed to research in topics: Receptor & Promoter. The author has an hindex of 5, co-authored 5 publications receiving 2286 citations.

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Cloning of the gene and cDNA for mammalian β -adrenergic receptor and homology with rhodopsin

TL;DR: Cloning of the gene and cDNA for the mammalian β2AR indicates significant amino-acid homology with bovine rhodopin and suggests that, like rhodopsin7, βAR possesses multiple membrane-spanning regions.
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cDNA for the human beta 2-adrenergic receptor: a protein with multiple membrane-spanning domains and encoded by a gene whose chromosomal location is shared with that of the receptor for platelet-derived growth factor.

TL;DR: A cDNA encoding the human beta 2-adrenergic receptor is isolated and sequenced, showing the most highly conserved regions are the putative transmembrane helices and cytoplasmic loops, suggesting that these regions of the molecule harbor important functional domains.
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Delineation of the intronless nature of the genes for the human and hamster beta 2-adrenergic receptor and their putative promoter regions.

TL;DR: A detailed characterization of its complete gene in both the human and hamster which reveals several unusual and provocative features suggest that the beta 2-adrenergic receptor may have arisen as a processed gene for another related gene.
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cAMP stimulates transcription of the beta 2-adrenergic receptor gene in response to short-term agonist exposure

TL;DR: The results establish the presence of elements within the proximal promoter region of the beta 2AR gene responsible for the transcriptional enhancing activity of cAMP and demonstrate that beta 2 AR gene expression is regulated by a type of feedback mechanism involving the second messenger cAMP.

Genetic regulation of {3-adrenergic receptors

TL;DR: In the last few years the genes for several of these receptors have been cloned and advances now permit a closer examination of the physical structure and the opportunity to examine directly their genetic regulation.