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Lista de obras de Dirce Carraro

A Region of the Cellobiohydrolase I Promoter from the Filamentous FungusTrichoderma reeseiMediates Glucose Repression inSaccharomyces cerevisiae,Dependent on Mitochondrial Activity

artículo científico publicado en 1998

A clinical, pathologic, and molecular study of p53 and murine double minute 2 in penile carcinogenesis and its relation to prognosis

artículo científico publicado en 2011

A genome survey of Moniliophthora perniciosa gives new insights into Witches' Broom Disease of cacao

artículo científico publicado en 2008

A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease.

artículo científico publicado en 2016

A novel SYBR-based duplex qPCR for the detection of gene dosage: detection of an APC large deletion in a familial adenomatous polyposis patient with an unusual phenotype

artículo científico publicado en 2012

A transcript finishing initiative for closing gaps in the human transcriptome

artículo científico publicado en 2004

A transcriptome-based signature of pathological angiogenesis predicts breast cancer patient survival

scientific article published on 17 December 2019

Abstract 3038: Determination of microRNA expression profile in tumors from young women with breast cancer

Abstract 3418: Rare germline copy number variations in hereditary cutaneous melanoma

Abstract 3427: Temporal analysis of kidney differentiation and Wilms tumor revealed conserved transcriptional mechanisms and pointed genes putatively determinant for tumor onset

article

Abstract 532: A transcriptional sketch of breast cancer fibroblasts: The validation of cDNA libraries for expression profile study using a high-throughput sequencing technology

Abstract 5598: Germline TP53 mutation in very early onset breast cancer patients without BRCA1 and BRCA2 mutation in Brazilian population

article

Abstract A025: Screening for genomic rearrangements and germline mutations in BRCA1 and BRCA2 genes in hereditary breast cancer unrelated Brazilian families

article

Abstract A24: Germline deletion at 3p12.3 in patients with hereditary breast and colorectal carcinoma

Alternative splicing enriched cDNA libraries identify breast cancer-associated transcripts

artículo científico publicado en 2010

Alternative splicing: a bioinformatics perspective

artículo científico publicado en 2007

Amyloid-β oligomers induce differential gene expression in adult human brain slices

artículo científico publicado en 2012

Analysis and functional annotation of an expressed sequence tag collection for tropical crop sugarcane

artículo científico publicado en 2003

Analysis of FOXP3 gene and protein expressions in renal allograft biopsies and their association with graft outcomes.

artículo científico

Assessment of somatic mutations in urine and plasma of Wilms tumor patients

artículo científico publicado en 2020

Association of Folate and Vitamins Involved in the 1-Carbon Cycle with Polymorphisms in the Methylenetetrahydrofolate Reductase Gene (MTHFR) and Global DNA Methylation in Patients with Colorectal Cancer

scientific article published on 18 June 2019

Association of melanoma with intraepithelial neoplasia of the pancreas in three patients.

artículo científico publicado en 2014

BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy

scientific article published on 09 November 2019

BRCA1 deficiency is a recurrent event in early-onset triple-negative breast cancer: a comprehensive analysis of germline mutations and somatic promoter methylation

artículo científico publicado en 2017

Biobanking and cytopathology: Challenges and opportunities from a Brazilian perspective.

artículo científico publicado en 2017

Biobanking practice: RNA storage at low concentration affects integrity

artículo científico publicado en 2014

Biomolecular analysis of matrix proteoglycans as biomarkers in non small cell lung cancer.

artículo científico publicado en 2018

Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: case report

artículo científico publicado en 2011

Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals.

artículo científico publicado en 2011

Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma.

artículo científico publicado en 2015

Clinical and Molecular Assessment of Patients with Lynch Syndrome and Sarcomas Underpinning the Association with MSH2 Germline Pathogenic Variants

artículo científico publicado en 2020

Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome

artículo científico publicado en 2015

Clinicopathological significance of ubiquitin-specific protease 2a (USP2a), fatty acid synthase (FASN), and ErbB2 expression in oral squamous cell carcinomas

artículo científico publicado en 2009

Closure of rRNA related gaps in the Chromobacterium violaceum genome with the PCR-assisted contig extension (PACE) protocol

scientific article published on 31 March 2004

Co-expression network of neural-differentiation genes shows specific pattern in schizophrenia

artículo científico publicado en 2015

Comparative analyses of the complete genome sequences of Pierce's disease and citrus variegated chlorosis strains of Xylella fastidiosa.

artículo científico publicado en 2003

Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.

artículo científico publicado en 2018

Comprehensive analysis of BRCA1, BRCA2 and TP53 germline mutation and tumor characterization: a portrait of early-onset breast cancer in Brazil

artículo científico publicado en 2013

Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genes

article

Correction: Poly (A)+Transcriptome Assessment of ERBB2-Induced Alterations in Breast Cell Lines

artículo científico publicado en 2011

DNA Methylation Levels of Melanoma Risk Genes Are Associated with Clinical Characteristics of Melanoma Patients

artículo científico publicado en 2015

DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations.

artículo científico publicado en 2016

DNA repair genes PAXIP1 and TP53BP1 expression is associated with breast cancer prognosis

artículo científico publicado en 2017

Deep Learning Predicts Underlying Features on Pathology Images with Therapeutic Relevance for Breast and Gastric Cancer

artículo científico publicado en 2020

Differential gene expression between the biotrophic-like and saprotrophic mycelia of the witches' broom pathogen Moniliophthora perniciosa

artículo científico publicado en 2008

Does germ-line deletion of the PIP gene constitute a widespread risk for cancer?

artículo científico publicado en 2013

Down-regulation of ANAPC13 and CLTCL1: Early Events in the Progression of Preinvasive Ductal Carcinoma of the Breast

artículo científico publicado en 2012

Ductal carcinoma in situ of the breast: morphological and molecular features implicated in progression

scientific article published on February 2014

Early gene expression changes in skeletal muscle from SOD1(G93A) amyotrophic lateral sclerosis animal model.

artículo científico publicado en 2014

Enhanced type I interferon gene signature in primary antiphospholipid syndrome: Association with earlier disease onset and preeclampsia

scientific article published on 14 February 2019

Epidermal growth factor receptor as an adverse survival predictor in squamous cell carcinoma of the penis.

artículo científico publicado en 2016

Epigenetic signature of differentially methylated genes in cutaneous melanoma

article

Epigenetic silencing of CRABP2 and MX1 in head and neck tumors

artículo científico

Epithelial cells captured from ductal carcinoma in situ reveal a gene expression signature associated with progression to invasive breast cancer

artículo científico publicado en 2016

Estrogen-responsive genes overlap with triiodothyronine-responsive genes in a breast carcinoma cell line

article

Evaluation of MLH1 I219V polymorphism in unrelated South American individuals suspected of having Lynch syndrome

artículo científico publicado en 2012

Evaluation of O6-methylguanine-DNA methyltransferase by immunohistochemistry: best clinical and research practices

artículo científico publicado en 2011

Evaluation of quantitative rt-PCR using nonamplified and amplified RNA.

artículo científico publicado en 2010

Evidence that molecular changes in cells occur before morphological alterations during the progression of breast ductal carcinoma

artículo científico publicado en 2008

Expanding morphological and clinical aspects of hereditary leiomyomatosis and renal cell carcinoma (HLRCC): a case report in a patient with unusual morphology and clinical presentation

scientific article published on 31 August 2018

Expression of putative pathogenicity-related genes in Xylella fastidiosa grown at low and high cell density conditions in vitro

artículo científico publicado en 2003

From Tissue Samples to Tumor Markers

From colorectal cancer pattern to the characterization of individuals at risk: picture for genetic research in Latin America

article

Gene Expression in Wilms Tumor: Disturbance of the Wnt Signaling Pathway and MicroRNA Biogenesis

artículo científico publicado en 2016

Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour.

artículo científico publicado en 2011

Gene expression arrays in cancer research: methods and applications

artículo científico publicado en 2005

Gene expression of peripheral blood lymphocytes may discriminate patients with schizophrenia from controls

article

Gene expression patterns through oral squamous cell carcinoma development: PD-L1 expression in primary tumor and circulating tumor cells

artículo científico publicado en 2015

Gene expression profile associated with response to doxorubicin-based therapy in breast cancer

artículo científico publicado en 2005

Gene expression profile of residual breast cancer after doxorubicin and cyclophosphamide neoadjuvant chemotherapy

article

Gene expression profile of stromal cells from potential metastatic sites in breast cancer patients.

artículo científico publicado en 2013

Gene expression profiling of clinical stages II and III breast cancer

article

Gene stage-specific expression in the microenvironment of pediatric myelodysplastic syndromes.

artículo científico publicado en 2006

Generation of longer 3' cDNA fragments from massively parallel signature sequencing tags

artículo científico publicado en 2004

Genetic and epigenetic characterization of the BRCA1 gene in Brazilian women at-risk for hereditary breast cancer.

scientific article published on December 2016

Genome-Wide Screening of mRNA Expression in Leprosy Patients

artículo científico publicado en 2015

Genome-wide DNA methylation profile of leukocytes from melanoma patients with and without CDKN2A mutations

artículo científico publicado en 2014

Genome-wide profiling of copy number alterations in triple-negative breast cancer identifies a region at 19p13 associated with lymph node metastasis.

artículo científico publicado en 2013

Genomic alteration in hereditary colorectal patients without mutations in mismatch repair genes

Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors.

artículo científico publicado en 2016

Germline BAX deletion in a patient with melanoma and gastrointestinal stromal tumor

artículo científico publicado en 2013

Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma.

artículo científico publicado en 2014

Germline DNA copy number variation in familial and early-onset breast cancer

artículo científico publicado en 2012

Germline Mutations in MLH1 Leading to Isolated Loss of PMS2 Expression in Lynch Syndrome: Implications for Diagnostics in the Clinic.

artículo científico publicado en 2017

Germline mutations in BRCA1 and BRCA2 in epithelial ovarian cancer patients in Brazil

artículo científico publicado en 2016

Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population

scientific article published on 10 February 2020

Hepatoblastomas exhibit marked <i>NNMT</i> downregulation driven by promoter DNA hypermethylation

scientific article published on 01 December 2020

Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients

artículo científico publicado en 2014

High Prevalence of EGFR Mutations in Lung Adenocarcinomas From Brazilian Patients Harboring the TP53 p.R337H Variant

artículo científico publicado en 2019

Hyaluronidase splice variants are associated with histology and outcome in adenocarcinoma and squamous cell carcinoma of the lung.

artículo científico publicado en 2011

Identification and complete sequencing of novel human transcripts through the use of mouse orthologs and testis cDNA sequences.

artículo científico publicado en 2004

Identification of Astyanax altiparanae (Teleostei, Characidae) in the Iguaçu River, Brazil, based on mitochondrial DNA and RAPD markers

article

Impact of BRCA1/2 Mutations on the Efficacy of Secondary Cytoreductive Surgery

artículo científico publicado en 2020

In silico characterization and expression analyses of sugarcane putative sucrose non-fermenting-1 (SNF1) related kinases

Increasing evidence for the presence of alternative proteins in human tissues and cell lines

article

Infections with multiple high-risk HPV types are associated with high-grade and persistent low-grade intraepithelial lesions of the cervix.

artículo científico publicado en 2016

Influence of BRCA1 Germline Mutations in the Somatic Mutational Burden of Triple-Negative Breast Cancer

artículo científico publicado en 2019

Influence of the interaction between nodal fibroblast and breast cancer cells on gene expression

artículo científico publicado en 2010

Innate immune response is differentially dysregulated between bipolar disease and schizophrenia

artículo científico publicado en 2014

Insights Into the Somatic Mutation Burden of Hepatoblastomas From Brazilian Patients

scientific article published on 05 May 2020

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation.

artículo científico publicado en 2010

Intratumoral heterogeneity of ADAM23 promotes tumor growth and metastasis through LGI4 and nitric oxide signals

artículo científico publicado en 2014

KRAS gene mutation in a series of unselected colorectal carcinoma patients with prognostic morphological correlations: a pyrosequencing method improved by nested PCR.

artículo científico publicado en 2015

KRAS insertions in colorectal cancer: what do we know about unusual KRAS mutations?

artículo científico publicado en 2014

KRAS mutation status is highly homogeneous between areas of the primary tumor and the corresponding metastasis of colorectal adenocarcinomas: one less problem in patient care

artículo científico publicado en 2017

LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis

artículo científico publicado en 2015

LINE-1 hypomethylation and mutational status in cutaneous melanomas

artículo científico publicado en 2016

Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion

artículo científico publicado en 2012

Linear mRNA amplification approach for RNAseq from limited amount of RNA.

artículo científico publicado en 2015

Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast

artículo científico publicado en 2014

MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicing

artículo científico publicado en 2020

MicroRNAs discriminate familial from sporadic non-BRCA1/2 breast carcinoma arising in patients ≤35 years.

artículo científico publicado en 2014

Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review

article

Mining ORESTES no-match database: can we still contribute to cancer transcriptome?

artículo científico publicado en 2006

Mismatch repair genes in Lynch syndrome: a review

artículo científico publicado en 2009

Molecular profiling of isolated histological components of wilms tumor implicates a common role for the Wnt signaling pathway in kidney and tumor development

artículo científico publicado en 2008

Multi-center real-world comparison of the fully automated Idylla™ microsatellite instability assay with routine molecular methods and immunohistochemistry on formalin-fixed paraffin-embedded tissue of colorectal cancer

artículo científico publicado en 2020

Multiple mutations in the Kras gene in colorectal cancer: review of the literature with two case reports

artículo científico publicado en 2011

Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient With Metastatic Colorectal Cancer

article published in 2018

Mutation spectrum in South American Lynch syndrome families

scientific article published on 18 December 2013

Mutational Portrait of Lung Adenocarcinoma in Brazilian Patients: Past, Present, and Future of Molecular Profiling in the Clinic

artículo científico publicado en 2020

Mutational Profile and New IASLC/ATS/ERS Classification Provide Additional Prognostic Information about Lung Adenocarcinoma: A Study of 125 Patients from Brazil

artículo científico publicado en 2015

Mutational spectrum of WTX, WT1, CTNNB1, APC and PLCG2 genes in Wilms tumor defined by massive parallel resequencing.

artículo científico publicado en 2012

Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients.

artículo científico publicado en 2013

Mutational status of VHL gene and its clinical importance in renal clear cell carcinoma.

artículo científico publicado en 2014

NDRG4 promoter hypermethylation is a mechanistic biomarker associated with metastatic progression in breast cancer patients

artículo científico publicado en 2019

No-match ORESTES explored as tumor markers

artículo científico publicado en 2009

P53 and expression of immunological markers may identify early stage thyroid tumors

artículo científico publicado en 2013

PRUNE2 is a human prostate cancer suppressor regulated by the intronic long noncoding RNA PCA3.

artículo científico publicado en 2015

Phosphodiesterase 11A (PDE11A) Genetic Variants May Increase Susceptibility to Prostatic Cancer.

artículo científico publicado en 2010

Phosphodiesterase 11A (PDE11A) genetic variants may increase susceptibility to prostatic cancer

artículo científico publicado en 2010

Phosphodiesterase sequence variants may predispose to prostate cancer

artículo científico publicado en 2015

Poly (A)+ transcriptome assessment of ERBB2-induced alterations in breast cell lines

artículo científico publicado en 2011

Polybromo-1 (PBRM1), a SWI/SNF complex subunit is a prognostic marker in clear cell renal cell carcinoma.

artículo científico publicado en 2013

Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries

artículo científico publicado en 2012

Prevalence of BRCA1 and BRCA2 pathogenic and likely pathogenic variants in non-selected ovarian carcinoma patients in Brazil

article

Primary cutaneous melanoma arising in agminated melanocytic nevi: CDKN2A and CDK4 mutation screening.

artículo científico publicado en 2012

Proficiency of DNA repair genes and microsatellite instability in operated colorectal cancer patients with clinical suspicion of lynch syndrome

artículo científico publicado en 2015

RAS mutations vary between lesions in synchronous primary colorectal cancer: testing only one lesion is not sufficient to guide anti-EGFR treatment decisions.

artículo científico publicado en 2015

ROBO1 deletion as a novel germline alteration in breast and colorectal cancer patients

scientific article published on 01 October 2015

Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development.

artículo científico publicado en 2017

Reciprocal changes in gene expression profiles of cocultured breast epithelial cells and primary fibroblasts.

artículo científico publicado en 2009

Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour

artículo científico publicado en 2014

Repair of oxidative DNA damage, cell-cycle regulation and neuronal death may influence the clinical manifestation of Alzheimer's disease

artículo científico publicado en 2014

Role of rare germline copy number variation in melanoma-prone patients

artículo científico publicado en 2016

S-score: a scoring system for the identification and prioritization of predicted cancer genes

artículo científico publicado en 2014

Sequencing technology status of BRCA1/2 testing in Latin American Countries

scientific article published on 02 June 2020

Structural features and transcript-editing analysis of sugarcane (Saccharum officinarum L.) chloroplast genome.

artículo científico publicado en 2004

Swine and poultry pathogens: the complete genome sequences of two strains of Mycoplasma hyopneumoniae and a strain of Mycoplasma synoviae

artículo científico publicado en 2005

TET Upregulation Leads to 5-Hydroxymethylation Enrichment in Hepatoblastoma

scientific article published on 12 June 2019

TGIF1 splicing variant 8 is overexpressed in oral squamous cell carcinoma and is related to pathologic and clinical behavior.

artículo científico publicado en 2013

TWIST1 is a molecular marker for a poor prognosis in oral cancer and represents a potential therapeutic target

artículo científico publicado en 2013

Temporal blastemal cell gene expression analysis in the kidney reveals new Wnt and related signaling pathway genes to be essential for Wilms' tumor onset

artículo científico publicado en 2011

The Genome Sequence of the Gram-Positive Sugarcane Pathogen Leifsonia xyli subsp. xyli

artículo científico publicado en 2004

The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome.

artículo científico publicado en 2001

The generation and utilization of a cancer-oriented representation of the human transcriptome by using expressed sequence tags

artículo científico publicado en 2003

The germline mutational landscape of BRCA1 and BRCA2 in Brazil.

artículo científico publicado en 2018

The human cell surfaceome of breast tumors

artículo científico publicado en 2013

The mitochondrial genome of the phytopathogenic basidiomycete Moniliophthora perniciosa is 109 kb in size and contains a stable integrated plasmid

artículo científico publicado en 2008

The mutational repertoire of uterine sarcomas and carcinosarcomas in a Brazilian cohort: A preliminary study

artículo científico publicado en 2021

The value of a tumor bank in the development of cancer research in Brazil: 13 years of experience at the a C camargo hospital

artículo científico publicado en 2012

Three Photobiomodulation Protocols in the Prevention/Treatment of Radiotherapy-induced Oral Mucositis

artículo científico publicado en 2020

Tissue hyaluronan expression, as reflected in the sputum of lung cancer patients, is an indicator of malignancy

artículo científico publicado en 2015

Training in molecular pathology during residency: the experience of a Brazilian hospital

article

Transcriptional alterations related to neuropathology and clinical manifestation of Alzheimer's disease.

artículo científico publicado en 2012

Transcriptional profile of fibroblasts obtained from the primary site, lymph node and bone marrow of breast cancer patients

artículo científico publicado en 2014

Tumor banking for health research in Brazil and Latin America: time to leave the cradle

article

Two new MLH1 germline mutations in Brazilian lynch syndrome families

article

Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas

artículo científico publicado en 2014

Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients

artículo científico publicado en 2020

Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer

scientific article published on 16 December 2020

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