BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia. (Q35124793)

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1 March 2020

title

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia (English)

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0 references

1

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Heather L Edward

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Lindsay A. Farrer

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Martin H Steinberg

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author name string

J J Farrell

2

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A Alsultan

3

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S Wang

4

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H Shappell

6

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H Bae

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J N Milton

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C T Baldwin

9

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A M Al-Rubaish

10

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Z Naserullah

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F Al-Muhanna

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A Alsuliman

13

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P K Patra

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D Ngo

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V Vathipadiekal

17

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D H K Chui

18

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A K Al-Ali

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publication date

30 January 2015

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Blood Cells, Molecules and Diseases

1 March 2020

published in

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volume

54

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1 March 2020

issue

3

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page(s)

224-230

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Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.

1 March 2020

cites work

1 reference

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An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level.

28 July 2018

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Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype

28 July 2018

1 reference

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Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans

28 July 2018

1 reference

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Genetic modifiers of sickle cell disease

28 July 2018

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Forced TR2/TR4 expression in sickle cell disease mice confers enhanced fetal hemoglobin synthesis and alleviated disease phenotypes

28 July 2018

1 reference

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Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencing

28 July 2018

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A functional element necessary for fetal hemoglobin silencing

28 July 2018

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Ancestry of African Americans with sickle cell disease

28 July 2018

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Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients

28 July 2018

1 reference

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Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

28 July 2018

1 reference

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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster

28 July 2018

1 reference

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Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A.

28 July 2018

1 reference

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BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies

28 July 2018

1 reference

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Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

28 July 2018

1 reference

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

28 July 2018

1 reference

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Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturations

28 July 2018

1 reference

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The cooperative study of sickle cell disease: review of study design and objectives.

28 July 2018

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Geographical survey of beta S-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation.

28 July 2018

1 reference

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Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type

28 July 2018

1 reference

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Haplotypes in tribal Indians bearing the sickle gene: evidence for the unicentric origin of the beta S mutation and the unicentric origin of the tribal populations of India

28 July 2018

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The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level

28 July 2018

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Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects

28 July 2018

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Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S

28 July 2018

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A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype

28 July 2018

1 reference

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Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.

27 September 2018

1 reference

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Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans

27 September 2018

1 reference

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DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

27 September 2018

1 reference

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Amplification-refractory mutation system (ARMS) analysis of point mutations.

27 September 2018

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cMYB is involved in the regulation of fetal hemoglobin production in adults.

27 September 2018

1 reference

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Estimation and tests of haplotype-environment interaction when linkage phase is ambiguous

27 September 2018

1 reference

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Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25703683

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Benign sickle-cell anaemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25703683

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25703683

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.BCMD.2015.01.001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25703683%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25703683%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

PubMed publication ID

25703683

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25703683%20AND%20SRC:MED&resulttype=core&format=json