(Q77470719)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9790504%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

title

Somatic mutations of the PTEN tumor suppressor gene in sporadic follicular thyroid tumors (English)

1 reference

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5 December 2019

author name string

N Halachmi

1

1 reference

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5 December 2019

S Halachmi

2

1 reference

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5 December 2019

E Evron

3

1 reference

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5 December 2019

P Cairns

4

1 reference

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5 December 2019

K Okami

5

1 reference

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5 December 2019

M Saji

6

1 reference

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5 December 2019

W H Westra

7

1 reference

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5 December 2019

M A Zeiger

8

1 reference

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5 December 2019

J Jen

9

1 reference

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5 December 2019

D Sidransky

10

1 reference

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5 December 2019

publication date

1 November 1998

1 reference

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Genes, Chromosomes and Cancer

5 December 2019

published in

1 reference

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5 December 2019

volume

23

1 reference

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5 December 2019

page(s)

239-243

1 reference

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5 December 2019

issue

3

1 reference

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Frequency of homozygous deletion at p16/CDKN2 in primary human tumours

5 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

Mutation and childhood cancer: a probabilistic model for the incidence of retinoblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

5' CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

Localization of the gene for Cowden disease to chromosome 10q22–23

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

Loss of heterozygosity for 10q loci in human gliomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

The Cowden syndrome: a clinical and genetic study in 21 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

Deletions of the long arm of chromosome 10 in progression of follicular thyroid tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199811%2923%3A3%3C239%3A%3AAID-GCC5%3E3.0.CO%3B2-2

10.1002/(SICI)1098-2264(199811)23:3<239::AID-GCC5>3.0.CO;2-2

21 January 2018

Identifiers

DOI

1 reference

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5 December 2019

1 reference