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1دورية أكاديمية
المؤلفون: Junea C. de Oliveira, Danilo V. Viana, Cleyton Zanardo, Erika M. M. Santos, André E. de Paula, Edenir I. Palmero, Benedito M. Rossi
المصدر: Cancer Medicine, Vol 8, Iss 5, Pp 2114-2122 (2019)
مصطلحات موضوعية: adenomatous polyposis coli, colorectal neoplasms, genotype, germline pathogenic variants, phenotype, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2045-7634Test
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2دورية أكاديمية
المؤلفون: Edenir I. Palmero, Henrique C.R. Galvão, Gabriela C. Fernandes, André E. de Paula, Junea C. Oliveira, Cristiano P. Souza, Carlos E. Andrade, Luis G.C. Romagnolo, Sahlua Volc, Maximiliano C. Neto, Cristina Sabato, Rebeca Grasel, Edmundo Mauad, Rui M. Reis, Rodrigo A.D. Michelli
المصدر: Genetics and Molecular Biology, Vol 39, Iss 2, Pp 168-177 (2016)
مصطلحات موضوعية: oncogenetics, hereditary cancer, public health, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://www.scielo.br/pdf/gmb/v39n2/1415-4757-gmb-1678-4685-GMB-2014-0364.pdfTest; http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572016000200168&tlng=enTest; https://doaj.org/toc/1678-4685Test
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3دورية أكاديمية
المؤلفون: Giovana T. Torrezan, Fernanda G. dos Santos R. de Almeida, Márcia C. P. Figueiredo, Bruna D. de Figueiredo Barros, Cláudia A. A. de Paula, Renan Valieris, Jorge E. S. de Souza, Rodrigo F. Ramalho, Felipe C. C. da Silva, Elisa N. Ferreira, Amanda F. de Nóbrega, Paula S. Felicio, Maria I. Achatz, Sandro J. de Souza, Edenir I. Palmero, Dirce M. Carraro
المصدر: Frontiers in Genetics, Vol 9 (2018)
مصطلحات موضوعية: cancer predisposition genes, hereditary breast cancer, whole-exome sequencing, germline pathogenic variants, cancer susceptibility, DNA repair genes, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://journal.frontiersin.org/article/10.3389/fgene.2018.00161/fullTest; https://doaj.org/toc/1664-8021Test
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4دورية أكاديمية
المؤلفون: Edenir I. Palmero, Maira Caleffi, Lavínia Schüler-Faccini, Fernanda L. Roth, Luciane Kalakun, Cristina Brinkmann Oliveira Netto, Giovana Skonieski, Juliana Giacomazzi, Bernadete Weber, Roberto Giugliani, Suzi A. Camey, Patricia Ashton-Prolla
المصدر: Genetics and Molecular Biology, Vol 32, Iss 3, Pp 447-455 (2009)
مصطلحات موضوعية: breast cancer, genetic counseling, hereditary cancer syndromes, Genetics, QH426-470
وصف الملف: electronic resource
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5دورية أكاديميةGenotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study
المؤلفون: Rui M B Maciel, Cleber P Camacho, Lígia V M Assumpção, Natassia E Bufalo, André L Carvalho, Gisah A de Carvalho, Luciana A Castroneves, Francisco M de Castro Jr, Lucieli Ceolin, Janete M Cerutti, Rossana Corbo, Tânia M B L Ferraz, Carla V Ferreira, M Inez C França, Henrique C R Galvão, Fausto Germano-Neto, Hans Graf, Alexander A L Jorge, Ilda S Kunii, Márcio W Lauria, Vera L G Leal, Susan C Lindsey, Delmar M Lourenço Jr, Léa M Z Maciel, Patrícia K R Magalhães, João R M Martins, M Cecília Martins-Costa, Gláucia M F S Mazeto, Anelise I Impellizzeri, Célia R Nogueira, Edenir I Palmero, Cencita H C N Pessoa, Bibiana Prada, Débora R Siqueira, Maria Sharmila A Sousa, Rodrigo A Toledo, Flávia O F Valente, Fernanda Vaisman, Laura S Ward, Shana S Weber, Rita V Weiss, Ji H Yang, Magnus R Dias-da-Silva, Ana O Hoff, Sergio P A Toledo, Ana L Maia
المصدر: Endocrine Connections, Vol 8, Iss 3, Pp 289-298 (2019)
مصطلحات موضوعية: RET, Brazil, multiple endocrine neoplasia, medullary thyroid carcinoma, pheochromocytoma, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
العلاقة: https://ec.bioscientifica.com/view/journals/ec/8/3/EC-18-0506.xmlTest; https://doaj.org/toc/2049-3614Test; https://doi.org/10.1530/EC-18-0506Test; https://doaj.org/article/37d0d78e06b24b48bb6c7725c95f14ccTest
الإتاحة: https://doi.org/10.1530/EC-18-0506Test
https://doaj.org/article/37d0d78e06b24b48bb6c7725c95f14ccTest -
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المؤلفون: Arcangela De Nicolo, Diana M. Eccles, Sarah Louise Ariansen, Michela Biancolella, Miguel de la Hoya, Orland Diez, Hans Ehrencrona, Florentia Fostira, Tiara Hassan, Issei Imoto, Artur Kowalik, Fabienne Lesueur, Arjen R. Mensenkamp, Heli Nevanlinna, Joanne Ngeow, Edenir I. Palmero, Inge Søkilde Pedersen, Frances Que, Jana Soukupová, Yen Tan, Ana Vega, Amanda B. Spurdle, Paolo Radice
المصدر: Cancer Research. 83:P6-02
مصطلحات موضوعية: Cancer Research, Oncology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::3b66afdd23fe5732d354631fbd677954Test
https://doi.org/10.1158/1538-7445.sabcs22-p6-02-15Test -
7دورية أكاديمية
المؤلفون: Juliana Giacomazzi, Marcia S Graudenz, Cynthia A B T Osorio, Patricia Koehler-Santos, Edenir I Palmero, Marcelo Zagonel-Oliveira, Rodrigo A D Michelli, Cristovam Scapulatempo Neto, Gabriela C Fernandes, Maria Isabel W S Achatz, Ghyslaine Martel-Planche, Fernando A Soares, Maira Caleffi, José Roberto Goldim, Pierre Hainaut, Suzi A Camey, Patricia Ashton-Prolla
المصدر: PLoS ONE, Vol 9, Iss 6, p e99893 (2014)
العلاقة: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24936644/pdf/?tool=EBITest; https://doaj.org/toc/1932-6203Test; https://doaj.org/article/ca12984e489e477ea53db1889f243b09Test
الإتاحة: https://doi.org/10.1371/journal.pone.0099893Test
https://doaj.org/article/ca12984e489e477ea53db1889f243b09Test -
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المؤلفون: Giovana T. Torrezan, Fernanda G. dos Santos R. de Almeida, Márcia C. P. Figueiredo, Bruna D. de Figueiredo Barros, Cláudia A. A. de Paula, Renan Valieris, Jorge E. S. de Souza, Rodrigo F. Ramalho, Felipe C. C. da Silva, Elisa N. Ferreira, Amanda F. de Nóbrega, Paula S. Felicio, Maria I. Achatz, Sandro J. de Souza, Edenir I. Palmero, Dirce M. Carraro
المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 9 (2018)
Repositório Institucional da UFRN
Universidade Federal do Rio Grande do Norte (UFRN)
instacron:UFRNمصطلحات موضوعية: 0301 basic medicine, Candidate gene, Cosegregation, lcsh:QH426-470, Biology, Germline, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, medicine, Genetics, whole-exome sequencing, Gene, CHEK2, Genetics (clinical), Exome sequencing, Original Research, DNA repair genes, hereditary breast cancer, medicine.disease, cancer susceptibility, lcsh:Genetics, 030104 developmental biology, 030220 oncology & carcinogenesis, Molecular Medicine, germline pathogenic variants, ERCC1, cancer predisposition genes
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ed201fa5325694820ae737c690e93e5Test
https://pubmed.ncbi.nlm.nih.gov/29868112Test -
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المؤلفون: Giovana T. Torrezan, Fernanda G. dos Santos R. de Almeida, Márcia C. P. Figueiredo, Bruna D. de Figueiredo Barros, Cláudia A. A. de Paula, Renan Valieris, Jorge E. S. de Souza, Rodrigo F. Ramalho, Felipe C. C. da Silva, Elisa N. Ferreira, Amanda F. de Nóbrega, Paula S. Felicio, Maria I. Achatz, Sandro J. de Souza, Edenir I. Palmero, Dirce M. Carraro
مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, cancer predisposition genes, hereditary breast cancer, whole-exome sequencing, germline pathogenic variants, cancer susceptibility, DNA repair genes
الإتاحة: https://doi.org/10.3389/fgene.2018.00161.s001Test
https://figshare.com/articles/dataset/Table_1_Complex_Landscape_of_Germline_Variants_in_Brazilian_Patients_With_Hereditary_and_Early_Onset_Breast_Cancer_DOCX/6226019Test -
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المؤلفون: Gabriela C. Fernandes, Rodrigo A.D. Michelli, Henrique C.R. Galvão, André E. Paula, Rui Pereira, Carlos E. Andrade, Paula S. Felicio, Cristiano P. Souza, Deise R.P. Mendes, Sahlua Volc, Gustavo N. Berardinelli, Rebeca S. Grasel, Cristina S. Sabato, Danilo V. Viana, José Carlos Machado, José Luis Costa, Edmundo C. Mauad, Cristovam Scapulatempo-Neto, Banu Arun, Rui M. Reis, Edenir I. Palmero
المساهمون: [et. al], Universidade do Minho
المصدر: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Oncotargetمصطلحات موضوعية: 0301 basic medicine, Gerontology, Heredity, Latin Americans, endocrine system diseases, DNA Mutational Analysis, Inheritance Patterns, Brca1 brca2, 0302 clinical medicine, Gene Frequency, Risk Factors, Medicine, c.5266dupC prevalence in brazil, skin and connective tissue diseases, Aged, 80 and over, Ovarian Neoplasms, HBOC in brazil, education.field_of_study, BRCA1 Protein, hereditary breast cancer, Middle Aged, genetic ancestry, Pedigree, 3. Good health, Phenotype, Oncology, 030220 oncology & carcinogenesis, Female, BRCA1/BRCA2 mutation profile in Brazil, Brazil, Research Paper, Hereditary Breast Cancer, Adult, Adolescent, Genetic genealogy, Population, Breast Neoplasms, Risk Assessment, Young Adult, 03 medical and health sciences, parasitic diseases, Biomarkers, Tumor, Humans, Genetic Predisposition to Disease, education, Germ-Line Mutation, Aged, BRCA2 Protein, Science & Technology, Native american, business.industry, Cancer, medicine.disease, 030104 developmental biology, Brazilian population, business, Demography
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea50d97e9492039220b2b671c2b26505Test
https://hdl.handle.net/1822/44880Test