标题
Genetic association studies in -hemoglobinopathies
作者
关键词
-
出版物
Hematology-American Society of Hematology Education Program
Volume 2013, Issue 1, Pages 354-361
出版商
American Society of Hematology
发表日期
2013-12-06
DOI
10.1182/asheducation-2013.1.354
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- (2013) Massimo Gentile et al. AMERICAN JOURNAL OF HEMATOLOGY
- Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia
- (2013) J. M. Flanagan et al. BLOOD
- Genetic determinants of haemolysis in sickle cell anaemia
- (2013) Jacqueline N. Milton et al. BRITISH JOURNAL OF HAEMATOLOGY
- Disruption of the Hbs1l-Myb Locus Causes Hereditary Persistence of Fetal Hemoglobin in a Mouse Model
- (2013) M. Suzuki et al. MOLECULAR AND CELLULAR BIOLOGY
- Lysine-specific demethylase 1 is a therapeutic target for fetal hemoglobin induction
- (2013) Lihong Shi et al. NATURE MEDICINE
- The Molecular Basis of -Thalassemia
- (2013) S. L. Thein Cold Spring Harbor Perspectives in Medicine
- Genetic modifiers of sickle cell disease
- (2012) Martin H. Steinberg et al. AMERICAN JOURNAL OF HEMATOLOGY
- Reawakening fetal hemoglobin: prospects for new therapies for the -globin disorders
- (2012) D. E. Bauer et al. BLOOD
- Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans
- (2012) H. T. Bae et al. BLOOD
- Silent cerebral infarcts: a review on a prevalent and progressive cause of neurologic injury in sickle cell anemia
- (2012) M. R. DeBaun et al. BLOOD
- Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia
- (2012) Mathula Thangarajh et al. BRITISH JOURNAL OF HAEMATOLOGY
- Genetic modifiers of -thalassemia and clinical severity as assessed by age at first transfusion
- (2012) F. Danjou et al. HAEMATOLOGICA
- Seventy-five genetic loci influencing the human red blood cell
- (2012) Pim van der Harst et al. NATURE
- A Genome-Wide Association Study of Total Bilirubin and Cholelithiasis Risk in Sickle Cell Anemia
- (2012) Jacqueline N. Milton et al. PLoS One
- The Ultimate Genetic Test
- (2012) R. Drmanac SCIENCE
- Genetic predictors for stroke in children with sickle cell anemia
- (2011) J. M. Flanagan et al. BLOOD
- The multifunctional role of EKLF/KLF1 during erythropoiesis
- (2011) M. Siatecka et al. BLOOD
- Fetal hemoglobin levels and morbidity in untransfused patients with -thalassemia intermedia
- (2011) K. M. Musallam et al. BLOOD
- MYH9 and APOL1 are both associated with sickle cell disease nephropathy
- (2011) Allison E. Ashley-Koch et al. BRITISH JOURNAL OF HAEMATOLOGY
- Dynamic long-range chromatin interactions controlMybproto-oncogene transcription during erythroid development
- (2011) Ralph Stadhouders et al. EMBO JOURNAL
- Variants in genetic modifiers of -thalassemia can help to predict the major or intermedia type of the disease
- (2011) C. Badens et al. HAEMATOLOGICA
- Erythroid phenotypes associated with KLF1 mutations
- (2011) J. Borg et al. HAEMATOLOGICA
- Genetic Modifiers of Sickle Cell Disease
- (2011) Swee Lay Thein HEMOGLOBIN
- Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
- (2011) Pallav Bhatnagar et al. JOURNAL OF HUMAN GENETICS
- Initial impact of the sequencing of the human genome
- (2011) Eric S. Lander NATURE
- Epigenome-wide association studies for common human diseases
- (2011) Vardhman K. Rakyan et al. NATURE REVIEWS GENETICS
- MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13
- (2011) V. G. Sankaran et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Correction of Sickle Cell Disease in Adult Mice by Interference with Fetal Hemoglobin Silencing
- (2011) J. Xu et al. SCIENCE
- Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia
- (2010) J. Makani et al. BLOOD
- The inherited diseases of hemoglobin are an emerging global health burden
- (2010) D. J. Weatherall BLOOD
- c-myb supports erythropoiesis through the transactivation of KLF1 and LMO2 expression
- (2010) E. Bianchi et al. BLOOD
- Transcriptional silencing of -globin by BCL11A involves long-range interactions and cooperation with SOX6
- (2010) J. Xu et al. GENES & DEVELOPMENT
- Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
- (2010) Joseph Borg et al. NATURE GENETICS
- KLF1 regulates BCL11A expression and γ- to β-globin gene switching
- (2010) Dewang Zhou et al. NATURE GENETICS
- Beta-thalassemia
- (2010) Renzo Galanello et al. Orphanet Journal of Rare Diseases
- Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans
- (2010) G. Genovese et al. SCIENCE
- Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment
- (2010) Kleber Yotsumoto Fertrin et al. Expert Review of Hematology
- Amelioration of Sardinian 0 thalassemia by genetic modifiers
- (2009) R. Galanello et al. BLOOD
- The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells
- (2009) K. Wahlberg et al. BLOOD
- A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E
- (2009) Manit Nuinoon et al. HUMAN GENETICS
- Chaperoning erythropoiesis
- (2008) M. J. Weiss et al. BLOOD
- The c-myb proto-oncogene and microRNA-15a comprise an active autoregulatory feedback loop in human hematopoietic cells
- (2008) H. Zhao et al. BLOOD
- BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies
- (2008) Amanda E. Sedgewick et al. BLOOD CELLS MOLECULES AND DISEASES
- MRI abnormalities of the brain in one-year-old children with sickle cell anemia
- (2008) Winfred C. Wang et al. PEDIATRIC BLOOD & CANCER
- Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of -thalassemia
- (2008) M. Uda et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- DNA polymorphisms at the BCL11A, HBS1L-MYB, and -globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
- (2008) G. Lettre et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific RepressorBCL11A
- (2008) Vijay G. Sankaran et al. SCIENCE
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