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Orlie Levy

Researcher at Albert Einstein College of Medicine

Publications -  15
Citations -  3620

Orlie Levy is an academic researcher from Albert Einstein College of Medicine. The author has contributed to research in topics: Symporter & Iodide transport. The author has an hindex of 14, co-authored 15 publications receiving 3484 citations. Previous affiliations of Orlie Levy include Yeshiva University.

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Cloning and characterization of the thyroid iodide transporter.

TL;DR: To the authors' knowledge, this is the first iodide-transporting molecule to have its cDNA cloned, providing a missing link in the thyroid hormone biosynthetic pathway.
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The mammary gland iodide transporter is expressed during lactation and in breast cancer

TL;DR: The results indicate that the mammary gland sodium/iodide symporter may be an essential breast cancer marker and that radioiodide should be studied as a possible option in the diagnosis and treatment of breast cancer.
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Thyroid Na+/I- symporter. Mechanism, stoichiometry, and specificity.

TL;DR: The rat thyroid Na+/I− symporter was expressed in Xenopus laevis oocytes and characterized using electrophysiological, tracer uptake, and electron microscopic methods to propose an ordered simultaneous transport mechanism in which the binding of Na+ to NIS occurs first.
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Molecular analysis of the sodium/iodide symporter: impact on thyroid and extrathyroid pathophysiology.

TL;DR: The continued molecular analysis of NIS clearly holds the potential of an even greater impact on a wide spectrum of fields, ranging from structure/function of transport proteins to the diagnosis and treatment of cancer, both in the thyroid and beyond.
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Post-transcriptional Regulation of the Sodium/Iodide Symporter by Thyrotropin

TL;DR: The results provide strong evidence of the major role played by post-transcriptional events in the regulation of NIS by TSH, and it is of medical significance that these TSH-dependent regulatory mechanisms may be altered in the large proportion of thyroid cancers in which NIS is predominantly expressed in intracellular compartments, instead of being properly targeted to the plasma membrane.