Organization of human δ- and β-globin genes in cellular DNA and the presence of intragenic inserts-Reference-Cited by-同舟云学术

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Organization of human δ- and β-globin genes in cellular DNA and the presence of intragenic inserts

Published:1978-09 Issue:1 Volume:15 Page:15-23
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Mears J.Gregory,Ramirez Francesco,Leibowitz David,Bank Arthur

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference17 articles.

1. The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion;Baglioni,1962

2. The thalassemia syndromes;Bank;Blood,1978

3. Polyadenylate sequences and biologic activity of human globin messenger ribonucleic acid;Cann;J. Biol. Chem.,1974

4. Chromosomal localization of human beta gene to human chromosome 11 on somatic cell hybrids;Deisseroth,1978

Cited by 130 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Effect of TATA Box polymorphisms in human β-globin gene promoter associated with β-thalassemia on interaction with TATA-binding protein;Russian Journal of Genetics: Applied Research;2011-05

2. Human Haemoglobin Genetics;Novartis Foundation Symposia;2008-05-30

3. Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and δβ° thalassemia patients;Experimental Hematology;2005-11

4. Delta Thalassemia: a Non-deletion Defect;European Journal of Biochemistry;2005-03-03

5. Fetal hemoglobin elevation in Hb lepore heterozygotes and its correlation with β globin cluster linked determinants;American Journal of Hematology;2002-01-18

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