Molecular basis of hereditary persistence of fetal hemoglobin (Q40850997)

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Language	Label	Description	Also known as
English	Molecular basis of hereditary persistence of fetal hemoglobin	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

review article

1 reference

stated in

Europe PubMed Central

title

Molecular basis of hereditary persistence of fetal hemoglobin (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

main subject

Hereditary persistence of fetal hemoglobin

0 references

author name string

Forget BG

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

language of work or name

English

0 references

publication date

1 June 1998

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

published in

Annals of the New York Academy of Sciences

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

volume

850

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

page(s)

38-44

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

cites work

Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end of the beta-globin gene cluster

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10460.X

retrieved

21 January 2018

Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10460.X

retrieved

21 January 2018

High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10460.X

retrieved

21 January 2018

Sequences located 3' to the breakpoint of the hereditary persistence of fetal hemoglobin-3 deletion exhibit enhancer activity and can modify the developmental expression of the human fetal A gamma-globin gene in transgenic mice.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10460.X

retrieved

21 January 2018

Methylation-Enhanced Binding of Sp1 to the Stage Selector Element of the Human γ-Globin Gene Promoter May Regulate Development Specificity of Expression

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1998.TB10460.X

retrieved

21 January 2018

Identifiers

DOI

10.1111/J.1749-6632.1998.TB10460.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

PubMed publication ID

9668525

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9668525

retrieved

24 September 2017

 

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