(Q34890572)

5 August 2017

title

Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin (English)

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5 August 2017

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3

Paolo Moi

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5 August 2017

Stefania Satta

1

1 reference

5 August 2017

Lucia Perseu

2

1 reference

5 August 2017

Isadora Asunis

4

1 reference

5 August 2017

Annalisa Cabriolu

5

1 reference

5 August 2017

Liliana Maccioni

6

1 reference

5 August 2017

Franca Rosa Demartis

7

1 reference

5 August 2017

Laura Manunza

8

1 reference

5 August 2017

Antonio Cao

9

1 reference

5 August 2017

Renzo Galanello

10

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5 August 2017

publication date

27 January 2011

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5 August 2017

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5 August 2017

volume

96

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5 August 2017

issue

5

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5 August 2017

page(s)

767-770

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describes a project that uses

5 August 2017

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3084925/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

Regulation of the human HBA genes by KLF4 in erythroid cell lines

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

Amelioration of Sardinian beta0 thalassemia by genetic modifiers

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

The erythroid phenotype of EKLF-null mice: defects in hemoglobin metabolism and membrane stability

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

Putting a finger on the switch

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

KLF1 regulates BCL11A expression and γ- to β-globin gene switching

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084925

Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21273267

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Alpha-thalassemia carrier identification by DNA analysis in the screening for thalassemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21273267

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3324/HAEMATOL.2010.037333

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5 August 2017

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5 August 2017

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