C. Albuquerque

发表

Clinical Impact of KRAS and GNAS Analysis Added to CEA and Cytology in Pancreatic Cystic Fluid Obtained by EUS-FNA

M. Cravo, J. P. da Silva, P. Chaves, 2018, Digestive Diseases and Sciences.

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

R. Henrique, M. Teixeira, S. Maia, 2019, Genes, chromosomes & cancer.

Aggressive Phenotype of MYH-Associated Polyposis with Jejunal Cancer and Intra-Abdominal Desmoid Tumor: Report of a Case

C. N. Leitão, I. Vitoriano, C. Baltazar, 2009, Diseases of the colon and rectum.

Serrated polyposis associated with a family history of colorectal cancer and/or polyps: The preferential location of polyps in the colon and rectum defines two molecular entities

C. N. Leitão, I. Vitoriano, R. Sousa, 2016, International journal of molecular medicine.

Polymethoxylated Flavones Target Cancer Stemness and Improve the Antiproliferative Effect of 5-Fluorouracil in a 3D Cell Model of Colorectal Cancer

A. Cifuentes, M. Bronze, A. Serra, 2019, Nutrients.

Association of colonic and endometrial carcinomas in Portuguese families with hereditary nonpolyposis colorectal carcinoma significantly increases the probability of detecting a pathogenic mutation in mismatch repair genes, primarily the MSH2 gene

M. Cravo, R. Sousa, A. Suspiro, 2004, Cancer.

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

M. M. Lemos, A. Dias Pereira, C. Albuquerque, 2017, Familial Cancer.

Colonic cancer in a 34-yr-old woman: should it prompt microsatellite instability studies and mismatch repair gene testing?

L. Glória, M. Cravo, C. N. Leitão, 1998, American Journal of Gastroenterology.

Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing

C. Cruz, M. Cravo, P. Chaves, 2002, Gut.

BRAF, KRAS and PIK3CA mutations in colorectal serrated polyps and cancer: Primary or secondary genetic events in colorectal carcinogenesis?

R. Hamelin, R. Seruca, F. Schmitt, 2008, BMC Cancer.

APC or MUTYH mutations account for the majority of clinically well‐characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas

M. Cravo, I. Vitoriano, C. Baltazar, 2009, Clinical genetics.

Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approach

R. Fodde, J. Burn, M. Cravo, 2000, European Journal of Human Genetics.

Colorectal Cancers Choosing Sides

E. Kuipers, R. Smits, E. Bakker, 2011 .

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

R. Fonseca, C. Albuquerque, Inês Francisco, 2022, Cancers.

The muir-torre syndrome: a rare variant of hereditary nonpolyposis colorectal cancer associated with hmsh2 mutation

M. Cravo, C. N. Leitão, F. Mira, 1998, American Journal of Gastroenterology.

Seven novel mutations in the APC gene of Portuguese families with familial adenomatous polyposis: correlation with phenotype.

M. Cravo, A. Suspiro, C. Albuquerque, 1999, Cancer genetics and cytogenetics.

Methylation changes at the GNAS imprinted locus in pancreatic cystic neoplasms are important for the diagnosis of malignant cysts

M. Cravo, P. Chaves, S. Faias, 2020, World journal of gastrointestinal oncology.

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

A. D. Pereira, P. Chaves, R. Fonseca, 2012, Familial Cancer.

Patient-Derived Explants of Colorectal Cancer: Histopathological and Molecular Analysis of Long-Term Cultures

C. Brito, E. Boghaert, V. E. Santo, 2021, Cancers.

The 'just-right' signaling model: APC somatic mutations are selected based on a specific level of activation of the beta-catenin signaling cascade.

R. Fodde, R. Smits, R. B. van der Luijt, 2002, Human molecular genetics.

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status.

L. Aaltonen, D. Arango, P. Laiho, 2004, Human molecular genetics.

BAT‐26 identifies sporadic colorectal cancers with mutator phenotype: a correlative study with clinico‐pathological features and mutations in mismatch repair genes

J. Soares, M. Cravo, C. Gaspar, 1999, The Journal of pathology.

Losses of heterozygosity on chromosomes 9p and 17p are frequent events in Barrett's metaplasia not associated with dysplasia or adenocarcinoma.

J. Soares, C. N. Leitão, A. D. Pereira, 2003 .

Losses of Heterozygosity on Chromosomes 9p and 17p Are Frequent Events in Barrett’s Metaplasia Not Associated With Dysplasia or Adenocarcinoma

J. Soares, C. N. Leitão, A. D. Pereira, 2003, American Journal of Gastroenterology.

Sporadic colorectal cancer: Studying ways to an end

I. Rosa, A. D. Pereira, P. Chaves, 2016, United European gastroenterology journal.

Wnt Signalling-Targeted Therapy in the CMS2 Tumour Subtype: A New Paradigm in CRC Treatment?

C. Albuquerque, Lucília Pebre Pereira, 2018, Advances in experimental medicine and biology.

Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or “multiple” colorectal adenomas

L. Lipton, O. Sieber, W. Bodmer, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Genetic characterisation of patients with multiple colonic polyps

C. Cruz, M. Cravo, C. N. Leitão, 2002, Journal of medical genetics.

Somatic Apc mutations are selected upon their capacity to inactivate the β‐catenin downregulating activity

R. Kucherlapati, R. Fodde, R. Smits, 2000, Genes, chromosomes & cancer.

Methylation patterns in dysplasia in inflammatory bowel disease patients

A. Peixoto, Marco Silva, P. Lago, 2020, Scandinavian journal of gastroenterology.

Inhibition of Fas expression by RNAi modulates 5-fluorouracil-induced apoptosis in HCT116 cells expressing wild-type p53.

C. Steer, Pedro M. Borralho, C. Rodrigues, 2007, Biochimica et biophysica acta.

Colorectal cancers choosing sides.

R. Smits, W. van Veelen, C. Albuquerque, 2011, Biochimica et biophysica acta.

Microsatellite instability in non-neoplastic mucosa of patients with ulcerative colitis: effect of folate supplementation

L. Glória, M. Cravo, C. N. Leitão, 1998, American Journal of Gastroenterology.

Targeting Colorectal Cancer Proliferation, Stemness and Metastatic Potential Using Brassicaceae Extracts Enriched in Isothiocyanates: A 3D Cell Model-Based Study

A. Serra, C. Duarte, L. Pereira, 2017, Nutrients.

Familial colorectal cancer type X syndrome: two distinct molecular entities?

C. N. Leitão, I. Vitoriano, A. D. Pereira, 2011, Familial Cancer.

Validation and simplification of Bethesda guidelines for identifying apparently sporadic forms of colorectal carcinoma with microsatellite instability

J. Soares, M. Cravo, P. Chaves, 1999, Cancer.

Colorectal Adenomas in Young Patients: Microsatellite Instability is not a Useful Marker to Detect New Cases of Lynch Syndrome

C. N. Leitão, R. Sousa, P. Chaves, 2008, Diseases of the colon and rectum.

Colorectal cancers show distinct mutation spectra in members of the canonical WNT signaling pathway according to their anatomical location and type of genetic instability

R. Fodde, R. Smits, I. Fonseca, 2010, Genes, chromosomes & cancer.

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

J. Serpa, C. Albuquerque, Inês Francisco, 2023, Lung cancer.

APC Somatic Mosaicism in a Patient with Gardner Syndrome Carrying the E1573X Mutation: Report of a Case

R. Vossen, C. Tops, C. Albuquerque, 2009, Diseases of the Colon & Rectum.

[Need of new clinical criteria for the identification of genetic Lynch syndrome].

R. Sousa, A. Suspiro, C. Albuquerque, 2007, Acta Médica Portuguesa.

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

M. Teixeira, A. Peixoto, P. Lopes, 2023, Cancers.

Combining the amplification refractory mutation system and high-resolution melting analysis for KRAS mutation detection in clinical samples

A. R. Fernandes, P. Baptista, B. Veigas, 2023, Analytical and Bioanalytical Chemistry.

Aggressive Phenotype of MYH-Associated Polyposis with Jejunal Cancer and Intra-Abdominal Desmoid Tumor: Report of a Case

C. N. Leitão, I. Vitoriano, C. Baltazar, 2009, Diseases of the colon and rectum.