Factor binding to the human gamma-globin gene distal CCAAT site: candidates for repression of the normal gene or activation of HPFH mutants.

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Analysis of the mechanism of action of non-deletion hereditary persistence of fetal hemoglobin mutants in transgenic mice.

P2860

Q39696919-91B2DCBE-6170-4557-82C3-5D9EA3EADF1F

P2860

Factor binding to the human gamma-globin gene distal CCAAT site: candidates for repression of the normal gene or activation of HPFH mutants.

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http://www.wikidata.org/entity/Q41009529

description

1998 nî lūn-bûn

@nan

1998年の論文

@ja

1998年論文

@yue

1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

1998年论文

@zh

1998年论文

@zh-cn

name

Factor binding to the human ga ...... or activation of HPFH mutants.

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type

Item

label

Factor binding to the human ga ...... or activation of HPFH mutants.

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Factor binding to the human ga ...... or activation of HPFH mutants.

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P1476

Factor binding to the human ga ...... or activation of HPFH mutants.

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P2093

Partington GA

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Patient RK

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P2860

A novel C-T transition within the distal CCAAT motif of the G gamma-globin gene in the Japanese HPFH: implication of factor binding in elevated fetal globin expression

DNA-binding specificities of the GATA transcription factor family

Nuclear proteins that bind the human gamma-globin gene promoter: alterations in binding produced by point mutations associated with hereditary persistence of fetal hemoglobin.

Use of yeast artificial chromosomes (YACs) in studies of mammalian development: production of beta-globin locus YAC mice carrying human globin developmental mutants.

A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin.

Regulation of GATA-2 phosphorylation by mitogen-activated protein kinase and interleukin-3.

Two promoter-specific host factors interact with adjacent sequences in an EIA-inducible adenovirus promoter.

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

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

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

P304

940-951

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P31

scholarly article

P356

10.1046/J.1365-2141.1998.00849.X

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P407

English

P433

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P478

102

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P577

1998-09-01T00:00:00Z

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P5875

13550456

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P698

9734644

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Factor binding to the human gamma-globin gene distal CCAAT site: candidates for repression of the normal gene or activation of HPFH mutants.

about

P2860

P2860

Factor binding to the human gamma-globin gene distal CCAAT site: candidates for repression of the normal gene or activation of HPFH mutants.

description

name

type

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698