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English
Mutational analysis of CDKN1B, a candidate tumor-suppressor gene, in refractory secondary/tertiary hyperparathyroidism
scientific article published on 20 February 2008
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
title
Mutational analysis of CDKN1B, a candidate tumor-suppressor gene, in refractory secondary/tertiary hyperparathyroidism
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
main subject
mutational analysis
1 reference
based on heuristic
inferred from title
author name string
K B Lauter
series ordinal
1
1 reference
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Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
A Arnold
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
language of work or name
English
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publication date
20 February 2008
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
published in
Kidney International
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
volume
73
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
issue
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
page(s)
1137-1140
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/ki.2008.28
0 references
cites work
Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clonal Chromosomal Defects in the Molecular Pathogenesis of Refractory Hyperparathyroidism of Uremia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New insights into the tumor suppression function of P27(kip1)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple functions of p27(Kip1) and its alterations in tumor cells: a review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of nuclear p27 (CDKN1B/KIP1) in colorectal cancer is correlated with microsatellite instability and CIMP.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The p27Kip1 tumor suppressor gene: Still a suspect or proven guilty?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reduced p18INK4c, p21CIP1/WAF1 and p27KIP1 mRNA levels in tumours of primary and secondary hyperparathyroidism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reduced p21, p27 and vitamin D receptor in the nodular hyperplasia in patients with advanced secondary hyperparathyroidism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tumour-suppressor genes: evolving definitions in the genomic age
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A polymorphism in the CDKN1B gene is associated with increased risk of hereditary prostate cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A single-nucleotide polymorphism in the human p27kip1 gene (-838C>A) affects basal promoter activity and the risk of myocardial infarction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p27(Kip1) stabilization and G(1) arrest by 1,25-dihydroxyvitamin D(3) in ovarian cancer cells mediated through down-regulation of cyclin E/cyclin-dependent kinase 2 and Skp1-Cullin-F-box protein/Skp2 ubiquitin ligase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FKI.2008.28
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/KI.2008.28
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
Dimensions Publication ID
1002725337
0 references
PubMed publication ID
18288099
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18288099
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
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