(Q37511873)

English

Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man. (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

0 references

Hereditary persistence of fetal hemoglobin

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beta thalassemia

1 reference

based on heuristic

inferred from title

author name string

Tuan D

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Feingold E

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Newman M

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Weissman SM

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Forget BG

5

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

1 November 1983

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

80

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

22

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

6937-6941

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

describes a project that uses

0 references

0 references

0 references

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Isolation and localization of DNA segments from specific human chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Polymorphism of DNA sequence in the beta-globin gene region. Application to prenatal diagnosis of beta 0 thalassemia in Sardinia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Purification of genomic sequences from bacteriophage libraries by recombination and selection in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

KpnI families of long, interspersed repetitive DNAs associated with the human β-globin gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Nonrandom association of polymorphic restriction sites in the β-globin gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Isolation of β-globin-related genes from a human cosmid library

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Introduction and Expression of a Fetal Human Globin Gene in Mouse Fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Physical mapping of the globin gene deletion in hereditary persistence of foetal haemoglobin (HPFH)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Restriction endonuclease mapping of the human γ globin gene loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Changes in restricted human cellular DNA fragments containing globin gene sequences in thalassemias and related disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

23 August 2017

Enhancer elements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

14 September 2017

Restriction mapping of a new deletion responsible forGγ(δβ)° thalassaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

14 September 2017

The structure of the human β-globin gene in β-thalassaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

14 September 2017

The deletion in a type of δ0-β0-thalassaemia begins in an inverted AluI repeat

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

26 June 2018

Absence of messenger RNA and gene DNA for beta-globin chains in hereditary persistence of fetal hemoglobin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

26 June 2018

Analysis of the beta-delta-globin gene loci in normal and Hb Lepore DNA: direct determination of gene linkage and intergene distance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

26 June 2018

DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

26 June 2018

Characterisation of deletions which affect the expression of fetal globin genes in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

26 June 2018

Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

26 June 2018

Deletion of the β-globin structure gene in hereditary persistence of foetal haemoglobin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

27 July 2018

Human fetal G gamma- and A gamma-globin genes: complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

2 September 2018

A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390101

2 September 2018

The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/6196781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/6196781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physical mapping of the globin gene deletion in (δβ)° - thalassaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/6196781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin

1 reference

https://pubmed.ncbi.nlm.nih.gov/6196781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Major rearrangement in the human β-globin gene cluster

1 reference

https://pubmed.ncbi.nlm.nih.gov/6196781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural features of the DNA flanking the human non-alpha globin genes: implications in the control of fetal hemoglobin switching

1 reference

https://pubmed.ncbi.nlm.nih.gov/6196781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhancer elements in immunoglobulin genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6196781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.80.22.6937

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1983PNAS...80.6937T

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

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