(Q34249835)

31 July 2017

A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin (English)

1 reference

31 July 2017

Berry M

1

1 reference

31 July 2017

Grosveld F

series ordinal

2

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31 July 2017

Dillon N

series ordinal

3

1 reference

31 July 2017

language of work or name

English

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publication date

1 August 1992

1 reference

31 July 2017

6 August 1992

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1379347

20 September 2022

1 reference

31 July 2017

358

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31 July 2017

499-502

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31 July 2017

6386

1 reference

https://scigraph.springernature.com/pub.10.1038/358499a0

31 July 2017

0 references

cites work

A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin

1 reference

7 January 2021

G to A substitution in the distal CCAAT box of the A gamma-globin gene in Greek hereditary persistence of fetal haemoglobin

1 reference

7 January 2021

Human γ-globin genes silenced independently of other genes in the β-globin locus

1 reference

7 January 2021

Position-independent, high-level expression of the human beta-globin gene in transgenic mice

1 reference

7 January 2021

Developmental regulation of human fetal-to-adult globin gene switching in transgenic mice.

1 reference

7 January 2021

Human gamma- to beta-globin gene switching in transgenic mice.

1 reference

7 January 2021

Importance of globin gene order for correct developmental expression.

1 reference

7 January 2021

A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemia

1 reference

7 January 2021

A single beta-globin locus control region element (5' hypersensitive site 2) is sufficient for developmental regulation of human globin genes in transgenic mice

1 reference

7 January 2021

Distal CCAAT box deletion in the A gamma globin gene of two black adolescents with elevated fetal A gamma globin

1 reference

7 January 2021

The deletion of the distal CCAAT box region of the A gamma-globin gene in black HPFH abolishes the binding of the erythroid specific protein NFE3 and of the CCAAT displacement protein

1 reference

7 January 2021

Human CCAAT-binding proteins have heterologous subunits

1 reference

7 January 2021

Regulated expression of globin chains and the erythroid transcription factor GATA-1 during erythropoiesis in the developing mouse

1 reference

7 January 2021

Transcriptional activation and DNA binding by the erythroid factor GF-1/NF-E1/Eryf 1.

1 reference

7 January 2021

trans-Activation of a globin promoter in nonerythroid cells

1 reference

7 January 2021

The human beta-globin gene 3' enhancer contains multiple binding sites for an erythroid-specific protein.

1 reference

7 January 2021

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

1 reference

7 January 2021

Identifiers

DOI

10.1038/358499A0

1 reference

Dimensions Publication ID

31 July 2017

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1 reference