Ines Francisco

Lisbon, Portugal

Last Updated: 09/26/2026

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Found 10 publications

A novel patient-derived cutaneous melanoma cell line reveals key features of metastatic melanoma.

A novel patient-derived cutaneous melanoma cell line reveals key features of metastatic melanoma.

Journal: Frontiers in oncology

Published: November 19, 2024

Germline Variants in DNA Interstrand-Cross Link Repair Genes May Contribute to Increased Susceptibility for Serrated Polyposis Syndrome.

Germline Variants in DNA Interstrand-Cross Link Repair Genes May Contribute to Increased Susceptibility for Serrated Polyposis Syndrome.

Journal: International journal of molecular sciences

Published: October 07, 2024

H2S-Synthesizing Enzymes Are Putative Determinants in Lung Cancer Management toward Personalized Medicine.

H2S-Synthesizing Enzymes Are Putative Determinants in Lung Cancer Management toward Personalized Medicine.

Journal: Antioxidants (Basel, Switzerland)

Published: December 05, 2023

Frequency of CDH1, CTNNA1 and CTNND1 Germline Variants in Families with Diffuse and Mixed Gastric Cancer.

Frequency of CDH1, CTNNA1 and CTNND1 Germline Variants in Families with Diffuse and Mixed Gastric Cancer.

Journal: Cancers

Published: July 12, 2023

NSCLC presents metabolic heterogeneity, and there is still some leeway for EGF stimuli in EGFR-mutated NSCLC.

NSCLC presents metabolic heterogeneity, and there is still some leeway for EGF stimuli in EGFR-mutated NSCLC.

Journal: Lung cancer (Amsterdam, Netherlands)

Published: April 20, 2023

Routine Immunohistochemical Analysis of Mismatch Repair Proteins in Colorectal Cancer-A Prospective Analysis.

Routine Immunohistochemical Analysis of Mismatch Repair Proteins in Colorectal Cancer-A Prospective Analysis.

Journal: Cancers

Published: June 10, 2022

Pediatric Colorectal Cancer: A Heterogenous Entity.

Pediatric Colorectal Cancer: A Heterogenous Entity.

Journal: Journal of pediatric hematology/oncology

Published: June 18, 2019

The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families.

The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families.

Journal: Genes, chromosomes & cancer

Published: February 13, 2019

A case of multiple gastrointestinal stromal tumors caused by a germline KIT gene mutation (p.Leu576Pro).

A case of multiple gastrointestinal stromal tumors caused by a germline KIT gene mutation (p.Leu576Pro).

Journal: Familial cancer

Published: October 25, 2016

Bethesda criteria for microsatellite instability testing: impact on the detection of new cases of Lynch syndrome.

Bethesda criteria for microsatellite instability testing: impact on the detection of new cases of Lynch syndrome.

Journal: Familial cancer

Published: July 11, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026