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Irwin M. Arias
Researcher at Albert Einstein College of Medicine
Publications - 96
Citations - 5472
Irwin M. Arias is an academic researcher from Albert Einstein College of Medicine. The author has contributed to research in topics: Bilirubin & Jaundice. The author has an hindex of 37, co-authored 96 publications receiving 5435 citations. Previous affiliations of Irwin M. Arias include Mount Desert Island Biological Laboratory & Centra.
Papers
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Two hepatic cytoplasmic protein fractions, Y and Z, and their possible role in the hepatic uptake of bilirubin, sulfobromophthalein, and other anions
TL;DR: Two hepatic cytoplasmic protein fractions, designated Y and Z, which bind sulfobromophthalein (BSP), bilirubin, and other organic anions, have been separated by G75 Sephadex gel filtration and appear to be important in the transfer of Organic anions from plasma into the liver.
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Ligandin: a Hepatic Protein which Binds Steroids, Bilirubin, Carcinogens and a Number of Exogenous Organic Anions
TL;DR: Three protein preparations from the rat liver 100,000g supernatant fraction have been independently purified to homogeneity, and they are basic azodye carcinogen-binding protein (β-ABP), corticosteroid Binder I3,4 and Y protein5.
Book
Glutathione, metabolism and function
Irwin M. Arias,William B. Jakoby +1 more
TL;DR: From the combination of knowledge and actions, someone can improve their skill and ability and this glutathione metabolism and function tells you, this will add more knowledge of you to life and work better.
Journal ArticleDOI
Multiple Forms of Human Glutathione S-Transferase and Their Affinity for Bilirubin
TL;DR: Evidence is presented that each of the purified species is homogeneous with respect to sodium dodecylsulfate-gel electrophoresis and binds bilirubin although this compound is not a substrate.
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The binding of fatty acids to cytoplasmic proteins: binding to Z protein in liver and other tissues of the rat.
TL;DR: A cytoplasmic binding protein (Z protein) has been shown to have a high affinity for fatty acids in rat liver, myocardium, skeletal muscle, intestinal mucosa, adipose tissue and kidney.