Molecular Basis of α-Thalassemia in Iran (Q47165286)

http://europepmc.org/abstract/PMC/5712386

10 January 2018

title

Molecular Basis of α-Thalassemia in Iran (English)

1 reference

http://europepmc.org/abstract/PMC/5712386

10 January 2018

author name string

Atefeh Valaei

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

Morteza Karimipoor

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

Alireza Kordafshari

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

Sirous Zeinali

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

publication date

1 January 2018

1 reference

http://europepmc.org/abstract/PMC/5712386

10 January 2018

published in

Iranian biomedical journal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

page(s)

6-14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran.

2 June 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran

23 May 2018

1 reference

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Evaluation of α-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

The Spectrum of α-Thalassemia Mutations in Kermanshah Province, West Iran.

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Spectrum of alpha-globin gene mutations among premarital Baluch couples in southeastern Iran

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

23 May 2018

1 reference

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Hematologic features of alpha thalassemia carriers

23 May 2018

1 reference

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Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

23 May 2018

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Clinical manifestations of α-thalassemia

23 May 2018

1 reference

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23 May 2018

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Prevalence of hemoglobin alpha-chain gene deletion in neonates in North of Iran.

23 May 2018

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The molecular basis of α-thalassemia: a model for understanding human molecular genetics

23 May 2018

1 reference

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Carrier screening for beta-thalassaemia: a review of international practice

23 May 2018

1 reference

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23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Hb H disease: clinical course and disease modifiers

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

23 May 2018

The alpha thalassaemias.

1 reference

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Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Iranian national thalassaemia screening programme

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Screening and genetic diagnosis of haemoglobin disorders

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Hemoglobin H disease: not necessarily a benign disorder.

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

An abundant erythroid protein that stabilizes free alpha-haemoglobin

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

The alpha-globin gene cluster: genetics and disorders

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias.

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Hydrops fetalis caused by alpha-thalassemia: an emerging health care problem.

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

High frequencies of alpha-thalassaemia are the result of natural selection by malaria

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

A review of the molecular genetics of the human alpha-globin gene cluster

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Introduction of novel α1-hemoglobin gene mutation with transfusion-dependent phenotype.

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Point mutations which should not be overlooked in Hb H disease

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Distribution of alpha-thalassemia mutations in Iranian population.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Heterogeneity of hemoglobin H disease in childhood

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Spectrum of α-Globin Gene Mutations in the Kerman Province of Iran

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Development of a quantitative real-time PCR assay for detection of unknown alpha-globin gene deletions.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Alpha-thalassemia mutations in Gilan Province, North Iran.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Variable clinical phenotypes of alpha-thalassemia syndromes.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Clinical features and molecular analysis in Thai patients with HbH disease

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutations

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

alpha-Thalassemia mutation analyses in Mazandaran province, North Iran

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

alpha-thalassemia mutations in Khuzestan Province, Southwest Iran

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Association between promoter and coding region mutations of UDP-glucuronosyltransferase 1A1 and beta-thalassemia/Hb E with cholelithiasis.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Molecular basis of Hb H disease in southwest Iran.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

High incidence of malaria in alpha-thalassaemic children

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5712386

Iranian national program for the prevention of thalassemia and prenatal diagnosis : mandatory premarital screening and legal medical abortion

15 August 2018

1 reference

12 December 2020

Genetic and clinical features of hemoglobin H disease in Chinese patients

1 reference

12 December 2020

Detection of deletions/duplications in α-globin gene cluster by multiplex ligation-dependent probe amplification

1 reference

12 December 2020

Genotype-phenotype correlation in Iranian patients with Hb H disease

1 reference

12 December 2020

Alpha thalassemia gene mutations in neonates from Mazandaran, Iran, 2012

1 reference

12 December 2020

α-Globin gene mutations in Isfahan Province, Iran

1 reference

12 December 2020

Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA]

1 reference

12 December 2020

Homozygosity for the AATAAA > AATA- - Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case Report

1 reference

12 December 2020

Rapid detection of six common Mediterranean and three non-Mediterranean alpha-thalassemia point mutations by reverse dot blot analysis

1 reference

12 December 2020

A novel molecular basis for beta thalassemia intermedia poses new questions about its pathophysiology

1 reference

12 December 2020

α-Thalassemia mutations in two provinces of Southern Iran: Fars & Kohkeloye and Bouyer Ahmad

1 reference

12 December 2020

Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient

1 reference

12 December 2020

Elucidating the spectrum of alpha-thalassemia mutations in Iran

1 reference

12 December 2020

Heterogeneity of hemoglobin h disease in childhood

1 reference

12 December 2020

Molecular spectrum of α‐thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects

1 reference

12 December 2020

Thalassemia in Iran: epidemiology, prevention, and management

1 reference

12 December 2020

Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH

1 reference

12 December 2020

Identifiers

DOI

10.22034/IBJ.22.1.6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

PubMed publication ID

29115104

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29115104%20AND%20SRC:MED&resulttype=core&format=json