(Q42808683)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18384130%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

title

Concomitant activation of Wnt pathway and loss of mismatch repair function in human melanoma (English)

1 reference

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5 January 2020

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3

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5 January 2020

Stefania D'Atri

10

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5 January 2020

author name string

Daniele Castiglia

1

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5 January 2020

Silvia Bernardini

2

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5 January 2020

Elena Pagani

4

1 reference

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5 January 2020

Naomi De Luca

5

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5 January 2020

Sabrina Falcinelli

6

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5 January 2020

Alberto Pacchiarotti

7

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5 January 2020

Enzo Bonmassar

8

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5 January 2020

Giovanna Zambruno

9

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5 January 2020

language of work or name

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1 July 2008

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Genes, Chromosomes and Cancer

5 January 2020

published in

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5 January 2020

volume

47

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5 January 2020

issue

7

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5 January 2020

page(s)

614-624

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describes a project that uses

5 January 2020

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Frequent nuclear/cytoplasmic localization of beta-catenin without exon 3 mutations in malignant melanoma

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The genetics of HNPCC: application to diagnosis and screening

21 January 2018

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7 January 2021

High-frequency microsatellite instability is associated with defective DNA mismatch repair in human melanoma.

1 reference

7 January 2021

Importance of P-cadherin, beta-catenin, and Wnt5a/frizzled for progression of melanocytic tumors and prognosis in cutaneous melanoma

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7 January 2021

Biallelic somatic inactivation of the mismatch repair gene MLH1 in a primary skin melanoma.

1 reference

7 January 2021

Detection and quantitation of melanoma cells in the circulation of patients.

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7 January 2021

Loss of membranous expression of beta-catenin is associated with tumor progression in cutaneous melanoma and rarely caused by exon 3 mutations

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7 January 2021

Bovine serum albumin reverses inhibition of RT-PCR by melanin

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7 January 2021

Wnt signaling in the intestinal epithelium: from endoderm to cancer

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7 January 2021

Adhesion, migration and communication in melanocytes and melanoma

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7 January 2021

Lessons from melanocyte development for understanding the biological events in naevus and melanoma formation

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7 January 2021

The multifaceted mismatch-repair system

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7 January 2021

Exon 3 beta-catenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome

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7 January 2021

Loss of beta-catenin expression associated with disease progression in malignant melanoma

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7 January 2021

Tissue microarray-based analysis shows phospho-beta-catenin expression in malignant melanoma is associated with poor outcome

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7 January 2021

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

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7 January 2021

The WNT/Beta-catenin pathway in melanoma

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7 January 2021

The clinical importance and prognostic implications of microsatellite instability in sporadic cancer

1 reference

7 January 2021

Mutation of the mismatch repair gene hMSH2 and hMSH6 in a human T-cell leukemia line tolerant to methylating agents.

1 reference

7 January 2021

Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling

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7 January 2021

Negative feedback loop of Wnt signaling through upregulation of conductin/axin2 in colorectal and liver tumors

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7 January 2021

Abnormalities of the APC/beta-catenin pathway in endometrial cancer

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7 January 2021

Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC

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7 January 2021

Cytoplasmic and nuclear accumulation of beta-catenin is rarely caused by CTNNB1 exon 3 mutations in cutaneous malignant melanoma

1 reference

7 January 2021

Mutation of a mutL homolog in hereditary colon cancer

1 reference

7 January 2021

The effect of O6-alkylguanine-DNA alkyltransferase and mismatch repair activities on the sensitivity of human melanoma cells to temozolomide, 1,3-bis(2-chloroethyl)1-nitrosourea, and cisplatin.

1 reference

7 January 2021

The many ways of Wnt in cancer

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7 January 2021

Mutations in exon 3 of the β-catenin gene are rare in melanoma cell lines

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7 January 2021

Molecular genetic analysis of malignant melanomas for aberrations of the WNT signaling pathway genes CTNNB1, APC, ICAT and BTRC.

1 reference

7 January 2021

APC mutations in sporadic colorectal tumors: A mutational "hotspot" and interdependence of the "two hits"

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7 January 2021

Stabilization of beta-catenin by genetic defects in melanoma cell lines

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7 January 2021

Colorectal cancer and genetic alterations in the Wnt pathway

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7 January 2021

Frequent alterations in the Wnt signaling pathway in colorectal cancer with microsatellite instability

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7 January 2021

Frequent activation of the beta-catenin-Tcf signaling pathway in nonfamilial colorectal carcinomas with microsatellite instability

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7 January 2021

E-cadherin/catenin complex in benign and malignant melanocytic lesions

1 reference

7 January 2021

Mutations within Wnt pathway genes in sporadic colorectal cancers and cell lines

1 reference

7 January 2021

Mutational spectrum of beta-catenin, AXIN1, and AXIN2 in hepatocellular carcinomas and hepatoblastomas

1 reference

7 January 2021

Genetic and epigenetic changes of components affecting the WNT pathway in colorectal carcinomas stratified by microsatellite instability

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7 January 2021

A Wnt-er wonderland--the complexity of Wnt signaling in melanoma

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7 January 2021

Genetic and epigenetic alterations of the APC gene in malignant melanoma

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7 January 2021

Somatic mutations of the PPP2R1B candidate tumor suppressor gene at chromosome 11q23 are infrequent in ovarian carcinomas

1 reference

7 January 2021

Elevated expression of axin2 and hnkd mRNA provides evidence that Wnt/beta -catenin signaling is activated in human colon tumors

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20567

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18384130%20AND%20SRC:MED&resulttype=core&format=json

release_3v6bqrapcre7dcgrjkjnhv2yxq

5 January 2020

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/3v6bqrapcre7dcgrjkjnhv2yxq

24 November 2022

mapped directly with Wikidata item

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