نتایج جستجو برای: beta globin introns

تعداد نتایج: 201054  

Journal: :Blood 1995
E Liakopoulou C A Blau Q Li B Josephson J A Wolf B Fournarakis V Raisys G Dover T Papayannopoulou G Stamatoyannopoulos

Butyrate, a four-carbon fatty acid, and its two-carbon metabolic product, acetate, are inducers of gamma-globin synthesis. To test whether other short-chain fatty acids share this property, we first examined whether propionic acid, a three-carbon fatty acid that is not catabolized to acetate, induces gamma-globin expression. Sodium propionate increased the frequency of fetal hemoglobin containi...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Saovaros Svasti Thipparat Suwanmanee Suthat Fucharoen Hong M Moulton Michelle H Nelson Nobuyo Maeda Oliver Smithies Ryszard Kole

Repair of beta-globin pre-mRNA rendered defective by a thalassemia-causing splicing mutation, IVS2-654, in intron 2 of the human beta-globin gene was accomplished in vivo in a mouse model of IVS2-654 thalassemia. This was effected by a systemically delivered splice-switching oligonucleotide (SSO), a morpholino oligomer conjugated to an arginine-rich peptide. The SSO blocked the aberrant splice ...

Journal: :Blood 1998
K Adachi T Yamaguchi J Pang S Surrey

Studies on assembly in vitro of alpha-globin chains with recombinant beta16 Gly-->Asp, beta95 Lys-->Glu, beta120 Lys-->Glu and beta16 Gly-->Asp, 120 Lys-->Glu human beta-globin chain variants in addition to human betaA- and betaS-globin chains were performed to evaluate effects of increased anionic charge in the beta chain on hemoglobin assembly using soluble recombinant beta-globin chains expr...

Journal: :Blood 2003
Stefania Bottardi Angelique Aumont Frank Grosveld Eric Milot

To study epigenetic regulation of the human beta-globin locus during hematopoiesis, we investigated patterns of histone modification and chromatin accessibility along this locus in hematopoietic progenitor cells (HPCs) derived from both humans and transgenic mice. We demonstrate that the developmentally related activation of human beta-like globin genes in humans and transgenic mice HPCs is pre...

Journal: :Molecular and cellular biology 2008
Tanushri Sengupta Ken Chen Eric Milot James J Bieker

Posttranslational modifications of transcription factors provide alternate protein interaction platforms that lead to varied downstream effects. We have investigated how the acetylation of EKLF plays a role in its ability to alter the beta-like globin locus chromatin structure and activate transcription of the adult beta-globin gene. By establishing an EKLF-null erythroid line whose closed beta...

Journal: :Nucleic acids research 1999
Gan Wang Xiaoxin Xu Betty Pace David A. Dean Peter M. Glazer Phillip Chan Steven R. Goodman Inna Shokolenko

Peptide nucleic acids (PNAs) can bind to homopurine/homopyrimidine sequences of double-stranded DNA targets in a sequence-specific manner and form [PNA]2/DNA triplexes with single-stranded DNA D-loop structures at the PNA binding sites. These D-loop structures have been found to have a capacity to initiate transcription in vitro. If this strategy can be used to induce transcription of endogenou...

Journal: :Trends in genetics : TIG 1999
Q Li S Harju K R Peterson

The beta-globin locus control region (LCR) is the founding member of a novel class of cis-acting regulatory elements that confer high level, tissue-specific, site-of-integration-independent, copy number-dependent expression on linked transgenes located in ectopic chromatin sites. Knowledge from beta-globin and other LCR studies has shed light on our understanding of the long-range interaction b...

2012
Haleh Akhavan-Niaki Ali Banihashemi Mandana Azizi

OBJECTIVE Four combinations of five neutral sequence changes at rs713040, rs10768683, rs7480526, rs7946748, and rs1609812 occurring in the human beta globin gene defined as frameworks have been reported in beta globin gene. Here we report for the frequency of these frameworks in thalassemia major patients of North Iran. METHODS Beta globin gene frameworks of 46 thalassemia major patients of N...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Suzan Imren Emmanuel Payen Karen A Westerman Robert Pawliuk Mary E Fabry Connie J Eaves Benjamin Cavilla Louis D Wadsworth Yves Beuzard Eric E Bouhassira Robert Russell Irving M London Ronald L Nagel Philippe Leboulch R Keith Humphries

Achieving long-term pancellular expression of a transferred gene at therapeutic level in a given hematopoietic lineage remains an important goal of gene therapy. Advances have recently been made in the genetic correction of the hemoglobinopathies by means of lentiviral vectors and large locus control region (LCR) derivatives. However, panerythroid beta globin gene expression has not yet been ac...

Journal: :international journal of hematology-oncology and stem cell research 0
fereshteh maryami biotechnology research center, department of molecular medicine, pasteur institute of iran, tehran, iran azita azarkeivan pediatric hematology oncology, transfusion research center, high institute for research and education in transfusion medicine, department of thalassemia clinic, tehran, iran mohammad sadegh fallah kawsar human genetics research center, tehran, iran sirous zeinali iranian molecular medicine network, biotechnology research center, pasteur institute of iran, pasteur st, tehran, iran kawsar human genetics research center, tehran, iran

background: thalassemia syndromes are the most prevalent single gene disorders in iran. this study aimed to evaluate the effect of different types of beta-globin gene mutations, co-inheritance of alpha-globin gene mutations and/or xmn1 snp on disease phenotype in a large cohort of iranian patients. subjects and methods: in total, 433 patients were clinically classified into β-thalassemia major ...

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