Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.
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Sickle cell disease in Middle East Arab countriesCurrent and future alternative therapies for beta-thalassemia majorGenomic approaches to identifying targets for treating β hemoglobinopathiesBeta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?DNA sequences regulating human globin gene transcription in nondeletional hereditary persistence of fetal hemoglobinNovel Inducers of Fetal Globin Identified through High Throughput Screening (HTS) Are Active In Vivo in Anemic Baboons and Transgenic MiceBeta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California.Intracellular polymerization. Disease severity and therapeutic predictions.beta(S)-Globin gene cluster haplotypes in the West Bank of Palestine.SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon.Can STOP Trial Velocity Criteria Be Applied to Iranian Children with Sickle Cell Disease?Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.Abundant raw material for cis-regulatory evolution in humans.Analysis of 5' flanking regions of the gamma globin genes from major African haplotype backgrounds associated with sickle cell disease.Hydroxyurea treatment in β-thalassemia patients: to respond or not to respond?Erythroid Kruppel-like factor is recruited to the CACCC box in the beta-globin promoter but not to the CACCC box in the gamma-globin promoter: the role of the neighboring promoter elements.Clinical findings associated with homozygous sickle cell disease in the Barbadian population--do we need a national SCD registry?Fetal hemoglobin in sickle cell anemiaAssociation of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon.Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haplotypes and are unrelated to fetal hemoglobin expressionFrom genotype to phenotype: genetics and medical practice in the new millennium.Potentially therapeutic levels of anti-sickling globin gene expression following lentivirus-mediated gene transfer in sickle cell disease bone marrow CD34+ cells.Haemoglobinopathies in southeast Asia.Modulating Effect of the -158 γ (C→T) Xmn1 Polymorphism in Indian Sickle Cell Patients.Genetic modifiers of sickle cell diseaseAmelioration of murine sickle cell disease by nonablative conditioning and γ-globin gene-corrected bone marrow cells.Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene.Pathophysiology and Clinical Manifestations of the β-Thalassemias.A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell diseaseDNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.Pharmacogenomics and therapeutics of hemoglobinopathies.Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation.Evidence of genetic interaction between the beta-globin complex and chromosome 8q in the expression of fetal hemoglobin.Control of fetal hemoglobin: new insights emerging from genomics and clinical implications.Fetal globin gene inducers: novel agents and new potential.A randomized phase I/II trial of HQK-1001, an oral fetal globin gene inducer, in β-thalassaemia intermedia and HbE/β-thalassaemia.Modifier genes in Mendelian disorders: the example of hemoglobin disorders.Diagnosis and prevention of thalassemia.Overview of the beta thalassemias: genetic and clinical aspects.
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Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on April 1985
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Common haplotype dependency of ...... d sickle cell anemia patients.
@en
Common haplotype dependency of ...... d sickle cell anemia patients.
@nl
type
label
Common haplotype dependency of ...... d sickle cell anemia patients.
@en
Common haplotype dependency of ...... d sickle cell anemia patients.
@nl
prefLabel
Common haplotype dependency of ...... d sickle cell anemia patients.
@en
Common haplotype dependency of ...... d sickle cell anemia patients.
@nl
P2093
P2860
P356
P1476
Common haplotype dependency of ...... d sickle cell anemia patients.
@en
P2093
C Beldjord
O Dunda-Belkhodja
P2860
P304
P356
10.1073/PNAS.82.7.2111
P407
P577
1985-04-01T00:00:00Z