Mutational analysis of CDKN1B, a candidate tumor-suppressor gene, in refractory secondary/tertiary hyperparathyroidism (Q80740235)

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3 January 2020

title

Mutational analysis of CDKN1B, a candidate tumor-suppressor gene, in refractory secondary/tertiary hyperparathyroidism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference

K B Lauter

1

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3 January 2020

A Arnold

series ordinal

2

1 reference

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3 January 2020

language of work or name

English

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publication date

20 February 2008

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3 January 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288099%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

volume

73

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3 January 2020

issue

10

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3 January 2020

page(s)

1137-1140

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https://scigraph.springernature.com/pub.10.1038/ki.2008.28

3 January 2020

exact match

0 references

cites work

Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia

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7 January 2021

Clonal Chromosomal Defects in the Molecular Pathogenesis of Refractory Hyperparathyroidism of Uremia

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7 January 2021

New insights into the tumor suppression function of P27(kip1)

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

Multiple functions of p27(Kip1) and its alterations in tumor cells: a review

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

Loss of nuclear p27 (CDKN1B/KIP1) in colorectal cancer is correlated with microsatellite instability and CIMP.

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

The p27Kip1 tumor suppressor gene: Still a suspect or proven guilty?

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

Reduced p18INK4c, p21CIP1/WAF1 and p27KIP1 mRNA levels in tumours of primary and secondary hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

Reduced p21, p27 and vitamin D receptor in the nodular hyperplasia in patients with advanced secondary hyperparathyroidism

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

Tumour-suppressor genes: evolving definitions in the genomic age

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

A polymorphism in the CDKN1B gene is associated with increased risk of hereditary prostate cancer

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

A single-nucleotide polymorphism in the human p27kip1 gene (-838C>A) affects basal promoter activity and the risk of myocardial infarction

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https://api.crossref.org/works/10.1038%2FKI.2008.28

7 January 2021

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

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7 January 2021