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English
Use of psoralen-coupled nucleotide primers for screening of COL4A5 mutations in Alport syndrome
scientific article published on 01 October 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
title
Use of psoralen-coupled nucleotide primers for screening of COL4A5 mutations in Alport syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
main subject
Alport syndrome
1 reference
based on heuristic
inferred from title
author name string
K O Netzer
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
S Seibold
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
O Gross
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
R Lambrecht
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
M Weber
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
language of work or name
English
0 references
publication date
1 October 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
published in
Kidney International
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
volume
50
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
page(s)
1363-1367
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ki.1996.450
0 references
cites work
HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Use of denaturing gradient gel electrophoresis to study conformational transitions in nucleic acids
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Psoralen-modified oligonucleotide primers improve detection of mutations by denaturing gradient gel electrophoresis and provide an alternative to GC-clamping
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of the COL4A5 gene in patients with Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
COL4A5 splice site mutation and alpha 5(IV) collagen mRNA in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of the gene for classic Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A splicing mutation in the alpha 5(IV) collagen gene of a family with Alport's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Photo-cross-linking of psoralen-derivatized oligonucleoside methylphosphonates to single-stranded DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the COL4A5 collagen gene in Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Major rearrangements in the α5(IV) collagen gene in three patients with alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA rearrangements in the α5(IV) collagen gene (COL4A5) of individuals with alport syndrome: Further refinement using pulsed-field gel electrophoresis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Different mutations in the COL4A5 collagen gene in two patients with different features of Alport syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.1996.450
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/KI.1996.450
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
PubMed publication ID
8887300
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8887300
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8887300%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
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