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Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
title
Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract
(English)
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
main subject
iron
1 reference
based on heuristic
inferred from title
author name string
C. Beaumont
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
P. Leneuve
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
I. Devaux
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
J. Y. Scoazec
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
M. Berthier
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
M. N. Loiseau
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
B. Grandchamp
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
D. Bonneau
series ordinal
8
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
language of work or name
English
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publication date
1 December 1995
1 reference
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PubMed
PubMed ID
7493028
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3 January 2017
published in
Nature Genetics
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
volume
11
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
page(s)
444–446
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
issue
4
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
exact match
https://scigraph.springernature.com/pub.10.1038/ng1295-444
0 references
cites work
Identification of the iron-responsive element for the translational regulation of human ferritin mRNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytoplasmic protein binds in vitro to a highly conserved sequence in the 5' untranslated region of ferritin heavy- and light-subunit mRNAs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Iron regulatory elements (IREs): a family of mRNA non-coding sequences
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regulating the fate of mRNA: the control of cellular iron metabolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ferritin: structure, gene regulation, and cellular function in animals, plants, and microorganisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human ferritin H and L sequences lie on ten different chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bilateral cataract and high serum ferritin: a new dominant genetic disorder?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Application of natural and amplification created restriction sites for the diagnosis of PKU mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Iron regulation of transferrin receptor mRNA levels requires iron-responsive elements and a rapid turnover determinant in the 3' untranslated region of the mRNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regulation of interaction of the iron-responsive element binding protein with iron-responsive RNA elements
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The interaction between the iron-responsive element binding protein and its cognate RNA is highly dependent upon both RNA sequence and structure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PROBABLE LINKAGE BETWEEN A CONGENITAL CATARACT LOCUS AND THE DUFFY BLOOD GROUP LOCUS
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A locus for a human hereditary cataract is closely linked to the gamma-crystallin gene family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A progressive early onset cataract gene maps to human chromosome 17q24.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Activation of the gamma E-crystallin pseudogene in the human hereditary Coppock-like cataract.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1295-444
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1295-444
0 references
PubMed ID
7493028
1 reference
stated in
PubMed
PubMed ID
7493028
retrieved
3 January 2017
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