(Q50500936)

English

Molecular analysis of the rare in(Lu) blood type: toward decoding the phenotypic outcome of haploinsufficiency for the transcription factor KLF1.

scientific article published on 2 November 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

Molecular analysis of the rare in(Lu) blood type: toward decoding the phenotypic outcome of haploinsufficiency for the transcription factor KLF1. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

haploinsufficiency

0 references

author name string

Virginie Helias

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

Carole Saison

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

Thierry Peyrard

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

Eliane Vera

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

Claude Prehu

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

Jean-Pierre Cartron

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

Lionel Arnaud

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

publication date

2 November 2012

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

34

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

221-228

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

Antigens Aua, i and P1 of cells of the dominant type of Lu(a-b-).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

Different inactivating mutations in the LU genes of three individuals with the Lutheran-null phenotype.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

Defective haematopoiesis in fetal liver resulting from inactivation of the EKLF gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

The multifunctional role of EKLF/KLF1 during erythropoiesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

Identification of a novel A4GALT exon reveals the genetic basis of the P1/P2 histo-blood groups.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

The Expected Blood-Group Antibody, anti-Lub

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

21 January 2018

A serological and genetical study of multiple antibodies formed in response to blood transfusion by a patient with lupus erythematosus diffusus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

7 January 2021

based on heuristic

inferred from DOI database lookup

The molecular basis of HPFH in a British family identified by heteroduplex formation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

7 January 2021

based on heuristic

inferred from DOI database lookup

The effect of In(Lu) on some high-frequency antigens

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

7 January 2021

based on heuristic

inferred from DOI database lookup

KLF1 gene mutations cause borderline HbA(2)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22218

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.22218

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23125034

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