Lista de obras - Branca M. Cavaco - Dominio Público Uruguay

A study of MECT1-MAML2 in mucoepidermoid carcinoma and Warthin's tumor of salivary glands.

artículo científico publicado en 2004

Cell cycle deregulation and TP53 and RAS mutations are major events in poorly differentiated and undifferentiated thyroid carcinomas

artículo científico publicado en 2014

Clinical and genetic characterization of Portuguese patients with pseudohypoparathyroidism type Ib.

artículo científico publicado en 2010

Clonal origin of non-medullary thyroid tumours assessed by non-random X-chromosome inactivation

scientific article published on 01 January 2002

Differential methylation as a cause of allele dropout at the imprinted GNAS locus

artículo científico publicado en 2010

Establishment and characterization of a new patient-derived anaplastic thyroid cancer cell line (C3948), obtained through fine-needle aspiration cytology

artículo científico publicado en 2019

Expression and function of the chemokine receptor CCR7 in thyroid carcinomas.

artículo científico publicado en 2006

Expression of vascular endothelial growth factor (VEGF) and its receptors in thyroid carcinomas of follicular origin: a potential autocrine loop.

artículo científico publicado en 2005

FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility

artículo científico publicado en 2012

Familial non-medullary thyroid carcinoma (FNMTC): analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations

scientific article published on 01 March 2008

Familial vs sporadic papillary thyroid carcinoma: a matched-case comparative study showing similar clinical/prognostic behaviour

artículo científico publicado en 2013

Gene expression profiling associated with the progression to poorly differentiated thyroid carcinomas

artículo científico publicado en 2009

High prevalence of RAS mutations in RET-negative sporadic medullary thyroid carcinomas.

artículo científico publicado en 2011

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene

artículo científico publicado en 2004

Hyperprolactinemia due to big big prolactin is differently detected by commercially available immunoassays.

artículo científico publicado en 1999

Identification and characterization of two novel germline RET variants associated with medullary thyroid carcinoma.

artículo científico publicado en 2015

Identification of De Novo Germline Mutations in the HRPT2 Gene in Two Apparently Sporadic Cases with Challenging Parathyroid Tumor Diagnoses

article

Identification of a novel CTR9 germline mutation in a family with Wilms tumor.

artículo científico publicado en 2017

Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC).

artículo científico publicado en 2014

Identification of somatic TERT promoter mutations in familial nonmedullary thyroid carcinomas

artículo científico publicado en 2017

Identification of the first germline HRPT2 whole-gene deletion in a patient with primary hyperparathyroidism

article

Mapping a New Familial Thyroid Epithelial Neoplasia Susceptibility Locus to Chromosome 8p23.1-p22 by High-Density Single-Nucleotide Polymorphism Genome-Wide Linkage Analysis

artículo científico publicado en 2008

Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22-q31

artículo científico publicado en 1999

Medullary Carcinomas of the Thyroid: A Monoclonal Origin

scientific article published on 01 December 2001

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism

artículo científico publicado en 2003

Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions

artículo científico publicado en 2002

Nobiletin Alone or in Combination with Cisplatin Decreases the Viability of Anaplastic Thyroid Cancer Cell Lines

scientific article published on 09 July 2019

Novel Mutation in the CASR Gene (p.Leu123Ser) in a Case of Autosomal Dominant Hypocalcemia.

artículo científico publicado en 2015

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.

artículo científico publicado en 2006

RAS proto-oncogene in medullary thyroid carcinoma

artículo científico publicado en 2015

Screening for a BRCA2 rearrangement in high-risk breast/ovarian cancer families: evidence for a founder effect and analysis of the associated phenotypes.

artículo científico publicado en 2007

Some forms of big big prolactin behave as a complex of monomeric prolactin with an immunoglobulin G in patients with macroprolactinemia or prolactinoma

scientific article published on 01 August 1995

TERT promoter mutations are a major indicator of poor outcome in differentiated thyroid carcinomas

artículo científico publicado en 2014

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome

artículo científico publicado en 2005

Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.

artículo científico publicado en 2014

Lista de obras de Branca M. Cavaco

A study of MECT1-MAML2 in mucoepidermoid carcinoma and Warthin's tumor of salivary glands.

Cell cycle deregulation and TP53 and RAS mutations are major events in poorly differentiated and undifferentiated thyroid carcinomas

Clinical and genetic characterization of Portuguese patients with pseudohypoparathyroidism type Ib.

Clonal origin of non-medullary thyroid tumours assessed by non-random X-chromosome inactivation

Differential methylation as a cause of allele dropout at the imprinted GNAS locus

Establishment and characterization of a new patient-derived anaplastic thyroid cancer cell line (C3948), obtained through fine-needle aspiration cytology

Expression and function of the chemokine receptor CCR7 in thyroid carcinomas.

Expression of vascular endothelial growth factor (VEGF) and its receptors in thyroid carcinomas of follicular origin: a potential autocrine loop.

FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility

Familial non-medullary thyroid carcinoma (FNMTC): analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations

Familial vs sporadic papillary thyroid carcinoma: a matched-case comparative study showing similar clinical/prognostic behaviour

Gene expression profiling associated with the progression to poorly differentiated thyroid carcinomas

High prevalence of RAS mutations in RET-negative sporadic medullary thyroid carcinomas.

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene

Hyperprolactinemia due to big big prolactin is differently detected by commercially available immunoassays.

Identification and characterization of two novel germline RET variants associated with medullary thyroid carcinoma.

Identification of De Novo Germline Mutations in the HRPT2 Gene in Two Apparently Sporadic Cases with Challenging Parathyroid Tumor Diagnoses

Identification of a novel CTR9 germline mutation in a family with Wilms tumor.

Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC).

Identification of somatic TERT promoter mutations in familial nonmedullary thyroid carcinomas

Identification of the first germline HRPT2 whole-gene deletion in a patient with primary hyperparathyroidism

Mapping a New Familial Thyroid Epithelial Neoplasia Susceptibility Locus to Chromosome 8p23.1-p22 by High-Density Single-Nucleotide Polymorphism Genome-Wide Linkage Analysis

Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22-q31

Medullary Carcinomas of the Thyroid: A Monoclonal Origin

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism

Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions

Nobiletin Alone or in Combination with Cisplatin Decreases the Viability of Anaplastic Thyroid Cancer Cell Lines

Novel Mutation in the CASR Gene (p.Leu123Ser) in a Case of Autosomal Dominant Hypocalcemia.

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.

RAS proto-oncogene in medullary thyroid carcinoma

Screening for a BRCA2 rearrangement in high-risk breast/ovarian cancer families: evidence for a founder effect and analysis of the associated phenotypes.

Some forms of big big prolactin behave as a complex of monomeric prolactin with an immunoglobulin G in patients with macroprolactinemia or prolactinoma

TERT promoter mutations are a major indicator of poor outcome in differentiated thyroid carcinomas

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome

Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.