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Molecular basis for dominantly inherited inclusion body beta-thalassemia
scientific journal article
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Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
title
Molecular basis for dominantly inherited inclusion body beta-thalassemia
(English)
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
main subject
beta thalassemia
1 reference
based on heuristic
inferred from title
author name string
S. L. Thein
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
C. Hesketh
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
P. Taylor
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
I. J. Temperley
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
R. M. Hutchinson
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
1971109
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4 January 2017
J. M. Old
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
W. G. Wood
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
1971109
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4 January 2017
J. B. Clegg
series ordinal
8
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
D. J. Weatherall
series ordinal
9
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
language of work or name
English
0 references
publication date
1 May 1990
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
volume
87
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
page(s)
3924–3928
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stated in
PubMed
PubMed ID
1971109
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4 January 2017
issue
10
1 reference
stated in
PubMed
PubMed ID
1971109
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4 January 2017
cites work
DNA sequencing with chain-terminating inhibitors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
20 March 2017
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
20 March 2017
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
20 March 2017
Characterization of a spontaneous mutation to a beta-thalassemia allele
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
29 September 2017
Direct cloning of specific genomic DNA sequences in plasmid libraries following fragment enrichment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
29 September 2017
Hemoglobin Cranston, an unstable variant having an elongated beta chain due to nonhomologous crossover between two normal beta chain genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
29 September 2017
Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
29 September 2017
Inclusion-body beta-thalassemia trait. A form of beta thalassemia producing clinical manifestations in simple heterozygotes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
2 June 2018
Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
2 June 2018
Heterozygous Beta Thalassaemia of Unusual Severity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
2 June 2018
One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
28 July 2018
A genetically determined disorder with features both of thalassaemia and congenital dyserythropoietic anaemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=54016
retrieved
27 November 2018
A novel globin structural mutant, Showa-Yakushiji (beta 110 Leu-Pro) causing a beta-thalassemia phenotype
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1971109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Molecular characterization of a high A2 beta thalassemia by direct sequencing of single strand enriched amplified genomic DNA
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1971109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Determination of alpha thalassaemia phenotypes by messenger RNA analysis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1971109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A family with segregating triplicated alpha globin loci and beta thalassemia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1971109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Thalassaemia intermedia: a new molecular basis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1971109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A new unstable haemoglobin variant: Hb Shanghai [beta 131(H9)Gln----Pro] found in China
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1971109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.87.10.3924
0 references
ADS bibcode
1990PNAS...87.3924T
0 references
PMCID
54016
0 references
PubMed ID
1971109
1 reference
stated in
PubMed
PubMed ID
1971109
retrieved
4 January 2017
ResearchGate publication ID
21185116
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