نتایج جستجو برای: globin

تعداد نتایج: 6744  

Journal: :American journal of physiology. Cell physiology 2014
Wei-Hwa Lee Ming-Hui Chung Yu-Hui Tsai Ju-Ling Chang Huei-Mei Huang

Interferon (IFN)-γ is a proinflammatory cytokine that is linked to erythropoiesis inhibition and may contribute to anemia. However, the mechanism of IFN-γ-inhibited erythropoiesis is unknown. Activin A, a member of the transforming growth factor (TGF)-β superfamily, induces the erythropoiesis of hematopoietic progenitor cells. In this study, a luciferase reporter assay showed that IFN-γ suppres...

2004
AeRi Kim

The mammalian -globin loci each contain a family of developmentally expressed genes, and a far upstream regulatory element, the locus control region (LCR). In adult murine erythroid cells, the LCR and the transcribed -globin genes exist within domains of histone acetylation and RNA polymerase II (pol II) is associated with them. In contrast, the silent embryonic genes lie between these domains ...

Journal: :Blood 1978
E Ullu M G Farace R Gambari P Orsi M Lunadei A Fantoni

The kinetic relationship between the globin mRNA accumulation and the rate of synthesis of globin chains was studied during the terminal stages of differentiation in erythroid cells derived from the yolk sac of mouse fetuses. RNA derived from the whole cells and from different cell compartments were hybridized to DNA complementary to embryonic globin mRNA. The relative proportion of embryonic g...

2017
Michael D. Gallagher Daniel J. Macqueen

The globin gene family encodes oxygen-binding hemeproteins conserved across the major branches of multicellular life. The origins and evolutionary histories of complete globin repertoires have been established for many vertebrates, but there remain major knowledge gaps for ray-finned fish. Therefore, we used phylogenetic, comparative genomic and gene expression analyses to discover and characte...

2018
Constantinos C. Loucari Petros Patsali Thamar B. van Dijk Coralea Stephanou Panayiota Papasavva Maria Zanti Ryo Kurita Yukio Nakamura Soteroulla Christou Maria Sitarou Sjaak Philipsen Carsten W. Lederer Marina Kleanthous

The β-hemoglobinopathies sickle cell anemia and β-thalassemia are the focus of many gene-therapy studies. A key disease parameter is the abundance of globin chains because it indicates the level of anemia, likely toxicity of excess or aberrant globins, and therapeutic potential of induced or exogenous β-like globins. Reversed-phase high-performance liquid chromatography (HPLC) allows versatile ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1973
D Housman B G Forget A Skoultchi E J Benz

A hybridization assay procedure was devised that makes possible quantitation of the ratio of mRNA of alpha to mRNA of beta globin chains in an RNA sample. The assay uses the radioactive synthetic DNA copies obtained by incubation of RNA-dependent DNA polymerase of avian myeloblastosis virus with rabbit globin mRNA that is 80-90% enriched in mRNA specific for synthesis of alpha or beta globin ch...

2003
Karin M. L. Gaensler Zemin Zhang Chin Lin Suya Yang Karin Hardt Linda Flebbe-Rehwaldt Mark T. Groudine Fred Hutchinson

The human -globin locus has been extensively studied as a model of tissue and developmental stage-specific gene expression. Structural mapping of naturally occurring mutations, including transfection and transgenic studies, and the recent finding of intergenic transcripts have suggested that there are cis-acting sequence elements in the A – intergenic region involved in regulating and -globin g...

Journal: :Blood 1989
M Albitar C Peschle S A Liebhaber

The theta globin gene is the most recently discovered member of the alpha globin gene family. Its pattern of expression during development is not fully defined, and its encoded protein has not yet been detected in vivo. The detection of theta globin messenger RNA (mRNA) in embryonic and fetal erythroid tissue but not in adults has suggested that theta is an embryonic globin gene. The present st...

2002
Jim Vadolas Hady Wardan Michael Orford Lucille Voullaire Faten Zaibak Robert Williamson Panayiotis A. Ioannou

Reactivation of fetal hemoglobin genes has been proposed as a potential therapeutic procedure in patients with β-thalassemia, sickle cell disease or other βhemoglobinopathies. In vitro model systems based on small plasmid globin gene constructs have previously been used in human and mouse erythroleukemic cell lines to study the molecular mechanisms regulating the expression of the fetal human g...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
T Ikuta S Ausenda M D Cappellini

Despite considerable concerns with pharmacological stimulation of fetal hemoglobin (Hb F) as a therapeutic option for the beta-globin disorders, the molecular basis of action of Hb F-inducing agents remains unclear. Here we show that an intracellular pathway including soluble guanylate cyclase (sGC) and cGMP-dependent protein kinase (PKG) plays a role in induced expression of the gamma-globin g...

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