BG FORGET - Annals of Internal Medicine, 1979 - Am Coll Physicians Molecular analysis of normal and abnormal human globin genes and their gene products has recently
provided information on the precise genetic events that result in hemoglobinopathies. In the case of
structurally abnormal hemoglobins, ... Cited by 39 - Related articles - All 2 versions
A Bank, JG Mears, F Ramirez - Science, 1980 - sciencemag.org Studies of the human hemoglobin system have provided new insights into the regulation of expression
of a group of linked human genes, the gamma-delta-beta-globin gene complex in man. In particular,
the thalassemia syndromes and ... Cited by 55 - Related articles - All 3 versions
DJ Weatherall, JB Clegg, D Weatherall, N Quattrin - Cell, 1979 - cell.com The β and δ chains of hemoglobins A and A are very similar in structure and are encoded by genes
that are tightly linked, yet in the red cell β chain production is 40 fold greater than production
of the δ chain, providing an ... Cited by 135 - Related articles - Cached - All 4 versions
D Schlessinger - Annual Review of Genetics, 1974 - Annual Reviews The details and ramifications of protein synthesis are so complex that all the avail able analytical
tools seem barely sufficient. The arsenal of physiological genetics is increasingly invaluable
because 1. genetic lesions are the ... Cited by 12 - Related articles - All 3 versions
[CITATION] Deletion of the/8-globin structure gene in hereditary persistence of foetal …
- ►pnas.org [PDF] LE Maquat, AJ Kinniburgh, LR Beach, … - Proceedings of the …, 1980 - National Acad Sciences Page 1. Proc. Nat!. Acad. Sci. USA Vol. 77, No. 7, pp. 4287-4291, July 1980 Medical Sciences Processing
of human f3-globin mRNA precursor to mRNA is defective in three patients with #+-thalassemia (nucleated
erythroid cells/globin RNA pulse-chase kinetics/RNA splicing) ... Cited by 58 - Related articles - All 7 versions
A Bank - Blood, 1978 - Am Soc Hematology . Hematology; all rights reserved Copyright 2007 by The American Society of DC 20036. by the
American Society of Hematology, 1900 M St, NW, Suite 200, Washington Blood (print ISSN 0006-4971,
online ISSN 1528-0020), is ... Cited by 57 - Related articles - All 4 versions
EJ Benz Jr, BG Forget - Annual Review of Medicine, 1982 - Annual Reviews The thalassemia syndromes are hereditary anemias characterized by defec tive synthesis of the a. or
fJ globin chains of human adult hemoglobin, Hb A (a.2Jh) (1, 2). For example, in fJ+-thalassemia fJ
chain synthesis is par tially ... Cited by 9 - Related articles - BL Direct - All 3 versions
