A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. - Wikidata - wikimedia - TriplyDB

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

http://www.wikidata.org/entity/Q34674466

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Advances in autism genetics: on the threshold of a new neurobiology Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin Hb E/beta-thalassaemia: a common & clinically diverse disorder Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Current and future alternative therapies for beta-thalassemia major Customizing the genome as therapy for the β-hemoglobinopathies Progress and promise in understanding the genetic basis of common diseases Genomic approaches to identifying targets for treating β hemoglobinopathies Fetal globin gene repressors as drug targets for molecular therapies to treat the β-globinopathies Sickle cell disease in children Using mouse models to study function of transcriptional factors in T cell development Role of the transcription factor Bcl11b in development and lymphomagenesis β-thalassemias: paradigmatic diseases for scientific discoveries and development of innovative therapies Therapeutic genome editing: prospects and challenges Erythro-megakaryocytic transcription factors associated with hereditary anemia Developmental and species-divergent globin switching are driven by BCL11A Global genetic architecture of an erythroid quantitative trait locus, HMIP-2 A HapMap harvest of insights into the genetics of common disease Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences.Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain Hemoglobin switching's surprise: the versatile transcription factor BCL11A is a master repressor of fetal hemoglobin.Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients.Chronic Lymphocytic Leukemia with Translocation (2;14)(p16;q32): A Case Report and Review of the Literature.Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study.Geographical genomics of human leukocyte gene expression variation in southern Morocco Chemical genetic strategy identifies histone deacetylase 1 (HDAC1) and HDAC2 as therapeutic targets in sickle cell disease.High-throughput genetic mapping of mutants via quantitative single nucleotide polymorphism typing SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon.Mutation analysis of β-thalassemia in East-Western Indian population: a recent molecular approach.Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster Transcriptional silencing of {gamma}-globin by BCL11A involves long-range interactions and cooperation with SOX6.An international effort to cure a global health problem: A report on the 19th Hemoglobin Switching Conference.Lysine-specific demethylase 1 is a therapeutic target for fetal hemoglobin induction Role of the GATA-1/FOG-1/NuRD pathway in the expression of human beta-like globin genes.KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of β-thalassemia Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA Eos negatively regulates human γ-globin gene transcription during erythroid differentiation.FOETAL HAEMOGLOBIN (HbF) STATUS IN ADULT SICKLE CELL ANAEMIA PATIENTS IN IBADAN, NIGERIA

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A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

http://www.wikidata.org/entity/Q34674466

description

2007 nî lūn-bûn

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2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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A QTL influencing F cell produ ...... er protein on chromosome 2p15.

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A QTL influencing F cell produ ...... er protein on chromosome 2p15.

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Anne Boland

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Chad Garner

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Fumihiko Matsuda

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Ivo Gut

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