Related references
Note: Only part of the references are listed.A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia
Lionel Arnaud et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Transcriptional silencing of γ-globin by BCL11A involves long-range interactions and cooperation with SOX6
Jian Xu et al.
GENES & DEVELOPMENT (2010)
Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic anemia mouse model
Daniel P. Heruth et al.
GENOMICS (2010)
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
Joseph Borg et al.
NATURE GENETICS (2010)
Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor
Miroslawa Siatecka et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants
Kamran Moradkhani et al.
ANNALS OF HEMATOLOGY (2009)
Genetic recombination as a major cause of mutagenesis in the human globin gene clusters
Joseph Borg et al.
CLINICAL BIOCHEMISTRY (2009)
Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype
Belinda K. Singleton et al.
BLOOD (2008)
Pharmacogenomics and therapeutics of hemoglobinopathies
George P. Patrinos et al.
HEMOGLOBIN (2008)
Silencing of Aγ-Globin gene expression during adult definitive erythropoiesis mediated by GATA-1-FOG-1-Mi2 complex binding at the -566 GATA site
Susanna Harju-Baker et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
Human variome microattribution reviews
[Anonymous]
NATURE GENETICS (2008)
Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific Repressor BCL11A
Vijay G. Sankaran et al.
SCIENCE (2008)
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea
Q. Ma et al.
PHARMACOGENOMICS JOURNAL (2007)
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
Stephan Menzel et al.
NATURE GENETICS (2007)
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait focus on chromosome 6q23 influencing fetal hemoglobin levels in adults
Swee Lay Thein et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Genome architecture of the human β-globin locus affects developmental regulation of gene expression
S Harju et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
LOVD: Easy creation of a locus-specific sequence variation database using an LSDB-in-a-Box approach
IFAC Fokkema et al.
HUMAN MUTATION (2005)
The erythroid phenotype of EKLF-null mice: Defects in hemoglobin metabolism and membrane stability
R Drissen et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Acquired α-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies
DP Steensma et al.
BLOOD (2005)
Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies
GP Patrinos et al.
NUCLEIC ACIDS RESEARCH (2004)
Flow cytometric analysis of fetal hemoglobin in erythroid precursors of β-thalassemia
I Amoyal et al.
CLINICAL AND LABORATORY HAEMATOLOGY (2004)
Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)
RJ Gibbons et al.
NATURE GENETICS (2003)
X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction
CN Yu et al.
BLOOD (2002)
HbVar. A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server
RC Hardison et al.
HUMAN MUTATION (2002)
Mutations in the general transcription factor TFIIH result in β-thalassaemia in individuals with trichothiodystrophy
V Viprakasit et al.
HUMAN MOLECULAR GENETICS (2001)
Share Paper
