Transferrin iron, chelatable iron and ferritin in idiopathic haemochromatosis. 1974

M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall

UI MeSH Term Description Entries
D007501 Iron A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN. Iron-56,Iron 56
D007502 Iron Chelating Agents Organic chemicals that form two or more coordination links with an iron ion. Once coordination has occurred, the complex formed is called a chelate. The iron-binding porphyrin group of hemoglobin is an example of a metal chelate found in biological systems. Iron Chelates,Agents, Iron Chelating,Chelates, Iron,Chelating Agents, Iron
D008297 Male Males
D011485 Protein Binding The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments. Plasma Protein Binding Capacity,Binding, Protein
D011863 Radioimmunoassay Classic quantitative assay for detection of antigen-antibody reactions using a radioactively labeled substance (radioligand) either directly or indirectly to measure the binding of the unlabeled substance to a specific antibody or other receptor system. Non-immunogenic substances (e.g., haptens) can be measured if coupled to larger carrier proteins (e.g., bovine gamma-globulin or human serum albumin) capable of inducing antibody formation. Radioimmunoassays
D001815 Bloodletting Puncture of a vein to draw blood for therapeutic purposes. Bloodletting therapy has been used in Talmudic and Indian medicine since the medieval time, and was still practiced widely in the 18th and 19th centuries. Its modern counterpart is PHLEBOTOMY.
D005293 Ferritins Iron-containing proteins that are widely distributed in animals, plants, and microorganisms. Their major function is to store IRON in a nontoxic bioavailable form. Each ferritin molecule consists of ferric iron in a hollow protein shell (APOFERRITINS) made of 24 subunits of various sequences depending on the species and tissue types. Basic Isoferritin,Ferritin,Isoferritin,Isoferritin, Basic
D006432 Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) Diabetes, Bronze,Bronze Diabetes,Bronzed Cirrhosis,Familial Hemochromatosis,Genetic Hemochromatosis,Haemochromatosis,Hemochromatoses,Iron Storage Disorder,Pigmentary Cirrhosis,Primary Hemochromatosis,Troisier-Hanot-Chauffard Syndrome,Von Recklenhausen-Applebaum Disease,Bronzed Cirrhoses,Cirrhoses, Bronzed,Cirrhoses, Pigmentary,Cirrhosis, Bronzed,Cirrhosis, Pigmentary,Disease, Von Recklenhausen-Applebaum,Diseases, Von Recklenhausen-Applebaum,Disorder, Iron Storage,Disorders, Iron Storage,Familial Hemochromatoses,Genetic Hemochromatoses,Haemochromatoses,Hemochromatose,Hemochromatoses, Familial,Hemochromatoses, Genetic,Hemochromatosis, Familial,Hemochromatosis, Genetic,Iron Storage Disorders,Pigmentary Cirrhoses,Recklenhausen-Applebaum Disease, Von,Recklenhausen-Applebaum Diseases, Von,Storage Disorder, Iron,Storage Disorders, Iron,Syndrome, Troisier-Hanot-Chauffard,Syndromes, Troisier-Hanot-Chauffard,Troisier Hanot Chauffard Syndrome,Troisier-Hanot-Chauffard Syndromes,Von Recklenhausen Applebaum Disease,Von Recklenhausen-Applebaum Diseases
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
June 1978, Gut,
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
July 1982, British journal of haematology,
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
March 1983, British medical journal (Clinical research ed.),
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
June 1983, British medical journal (Clinical research ed.),
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
May 1952, Klinische Wochenschrift,
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
November 1985, The Journal of biological chemistry,
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
March 1975, Gut,
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
December 1981, British journal of haematology,
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
January 1986, Scandinavian journal of haematology,
M R Beamish, and R Walker, and F Miller, and M Worwood, and A Jacobs, and R Williams, and A Corrigall
March 1993, Transfusion medicine (Oxford, England),
Copied contents to your clipboard!