(Q36011936)

English

Molecular characterization of a novel form of (A gamma delta beta)zero-thalassemia deletion with a 3' breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Molecular characterization of a novel form of (A gamma delta beta)zero-thalassemia deletion with a 3' breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

author name string

N P Anagnou

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

T Papayannopoulou

2

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

A W Nienhuis

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

G Stamatoyannopoulos

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

language of work or name

0 references

publication date

1 July 1988

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

16

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

13

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

6057-6066

1 reference

Europe PubMed Central

PMC publication ID

11 August 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=336847

2 October 2017

Cloning and characterization of DNA sequences surrounding the human gamma-, delta-, and beta-globin genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 2017

Direct evidence for interaction between human erythroid progenitor cells and a hemoglobin switching activity present in fetal sheep serum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 2017

Hemoglobin switching in culture: evidence for a humoral factor that induces switching in adult and neonatal but not fetal erythroid cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 2017

Identification of a retrovirus-like repetitive element in human DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 2017

Analysis of an inversion within the human beta globin gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 2017

An enhancer element lies 3' to the human A gamma globin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 2017

A Chinese G gamma + (A gamma delta beta)zero thalassemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpoints

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 2017

Italian type of deletional 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=336847

2 October 2017

A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 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=336847

2 October 2017

Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

2 October 2017

A haemoglobin switching activity modulates 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=336847

11 July 2018

Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G? and A? types of ? chain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

11 July 2018

The human beta-interferon gene enhancer is under negative control

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

11 July 2018

(A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

11 July 2018

Hereditary persistence of fetal hemoglobin or (delta beta)o-thalassemia: three types observed in South-Chinese families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=336847

11 July 2018

Analysis of mutations associated with deletion and nondeletion 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=336847

11 July 2018

Homozygosity for a new type of G gamma (A gamma delta beta)zero-thalassemia in a Malaysian male

1 reference

https://pubmed.ncbi.nlm.nih.gov/2456521

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/2456521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

(A gamma delta beta) thalassaemia: similarity of phenotype in four different molecular defects, including one newly described

1 reference

https://pubmed.ncbi.nlm.nih.gov/2456521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2456521

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/16.13.6057

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

DBLP publication ID

journals/nar/AnagnouPNs88

1 reference

DBLP Dataset 2021-01-02

28 January 2021

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36011936&oldid=1979858939"