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1دورية أكاديميةNucleocapsid single point-mutation associated with drop-out on RT-PCR assay for SARS-CoV-2 detection
المؤلفون: Fernanda de Mello Malta, Deyvid Amgarten, Alexandre Rodrigues Marra, Roberta Cardoso Petroni, Luiz Henrique da Silva Nali, Ricardo Andreotti Siqueira, Miguel Cendoroglo Neto, Silvia Cassiano Oler, João Renato Rebello Pinho
المصدر: BMC Infectious Diseases, Vol 23, Iss 1, Pp 1-7 (2023)
مصطلحات موضوعية: SARS-CoV-2, Viral agent, Genomic data, Molecular tests, Vaccines, Infectious and parasitic diseases, RC109-216
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1471-2334
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2دورية أكاديمية
المؤلفون: Roberta Cardoso Petroni, Anelisie da Silva Santos, Marcio Anunciação Menezes, Ana Paula Moreira Salles, Alexandre Hideaki Takara, Fernanda de Mello Malta, Deyvid Emanuel Amgarten, Raquel Riyuzo de Almeida Franco, Andrea Ap. Rocco Villarinho, Rubia Anita Ferraz Santana, Andre Mario Doi, Gustavo Bruniera Peres Fernandes, João Renato Rebello Pinho
المصدر: Brazilian Journal of Infectious Diseases, Vol 26, Iss , Pp 102199- (2022)
مصطلحات موضوعية: Infectious and parasitic diseases, RC109-216, Microbiology, QR1-502
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Luis Eduardo Silva Machado, João Renato Rebello Pinho, Roberta Sitnik, Nair Hideko Muto, Elvira Deolinda Rodrigues Pereira Velloso, Roberta Cardoso Petroni, Paulo Vidal Campregher
المصدر: Einstein (São Paulo), Vol 10, Iss 3, Pp 286-291 (2012)
مصطلحات موضوعية: Leucemia mieloide aguda, Receptores proteína tirosina quinases, Fatores de ligação ao core, Expressão gênica, Medicine
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Luis Eduardo Silva Machado, João Renato Rebello Pinho, Roberta Sitnik, Nair Hideko Muto, Elvira Deolinda Rodrigues Pereira Velloso, Roberta Cardoso Petroni, Paulo Vidal Campregher
المصدر: Einstein (São Paulo), Vol 10, Iss 3, Pp 286-291 (2012)
مصطلحات موضوعية: Leukemia, myeloid, acute, Receptor protein-tyrosine kinase, Core binding factors, Gene expression, Medicine
وصف الملف: electronic resource
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5دورية أكاديمية
المؤلفون: Paulo Vidal Campregher, Welbert de Oliveira Pereira, Bianca Lisboa, Renato Puga, Elvira Rodrigues Pereira Velloso Deolinda, Ricardo Helman, Luciana Cavalheiro Marti, João Carlos Campos Guerra, Kalliopi N. Manola, Roberta Cardoso Petroni, Alanna Mara Pinheiro Sobreira Bezerra, Fernando Ferreira Costa, Nelson Hamerschlak, Fábio Pires de Souza Santos
المصدر: Haematologica, Vol 101, Iss 7 (2016)
مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
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6دورية أكاديمية
المؤلفون: Roberta Sitnik, Alexandre Rodrigues Marra, Roberta Cardoso Petroni, Ozires Pereira Santos Ramos, Marinês Dalla Valle Martino, Jacyr Pasternak, Oscar Fernando Pavão dos Santos, Cristóvão Luis Pitangueira Mangueira, João Renato Rebello Pinho
المصدر: Einstein (São Paulo), Vol 12, Iss 2, Pp 191-196
مصطلحات موضوعية: Sepse/diagnóstico, Reação multiplex em cadeia da polimerase, Reação em cadeia da polimerase em tempo real, Medicine
وصف الملف: electronic resource
Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082014000200191&lng=en&tlng=en; https://doaj.org/toc/2317-6385
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7دورية أكاديمية
المؤلفون: Roberta Cardoso Petroni, Susana Elaine Alves da Rosa, Flavia Pereira de Carvalho, Rúbia Anita Ferraz Santana, Joyce Esteves Hyppolito, Claudia Mac Donald Bley Nascimento, Nelson Hamerschlak, Paulo Vidal Campregher
المصدر: Einstein (São Paulo), Vol 15, Iss 4, Pp 492-495
مصطلحات موضوعية: Ferritins, Cataract, Point mutation, Genetics, Heredity, Case reports, Medicine
وصف الملف: electronic resource
Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082017000400492&lng=en&tlng=en; https://doaj.org/toc/2317-6385
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المؤلفون: Claudia Mac Donald Bley Nascimento, Joyce E Hyppolito, Paulo Vidal Campregher, Susana Elaine Alves da Rosa, Nelson Hamerschlak, Roberta Cardoso Petroni, Flavia Pereira de Carvalho, Rúbia Anita Ferraz Santana
المصدر: Einstein
Einstein (São Paulo), Vol 15, Iss 4, Pp 492-495مصطلحات موضوعية: 0301 basic medicine, Heredity, Mutação puntual, lcsh:Medicine, Case Report, Catarata, Gene mutation, Bioinformatics, medicine.disease_cause, Cataract, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, medicine, Genetics, Hemochromatosis, Sanger sequencing, Point mutation, Case reports, Relatos de casos, biology, business.industry, lcsh:R, Genetic disorder, General Medicine, medicine.disease, Genética, Ferritin, Ferritin light chain, Hereditariedade, 030104 developmental biology, 030220 oncology & carcinogenesis, Ferritins, symbols, biology.protein, Ferritinas, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a45b9dc18c478cb66fdacc596efdf6b
http://europepmc.org/articles/PMC5875167 -
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المؤلفون: Fernando Ferreira Costa, Elvira Deolinda Rodrigues Pereira Velloso, Kalliopi N. Manola, Luciana Cavalheiro Marti, Roberta Cardoso Petroni, Nelson Hamerschlak, Alanna Mara P. S. Bezerra, Fabio P. Santos, João Carlos de Campos Guerra, Paulo Vidal Campregher, Ricardo Helman, Welbert Oliveira Pereira, Renato David Puga, Bianca Lisboa
مصطلحات موضوعية: 0301 basic medicine, NPM1, RUNX1T1, Myeloid leukemia, Hematology, Biology, medicine.disease, Molecular biology, Frameshift mutation, Fusion gene, 03 medical and health sciences, Leukemia, 030104 developmental biology, medicine, Nuclear protein, Nuclear export signal, Online Only Articles
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec06faf57e061ceb276d89bb0e118a4b
https://europepmc.org/articles/PMC5004474/ -
10A Novel Assay for the Identification of NOTCH1 PEST Domain Mutations in Chronic Lymphocytic Leukemia
المؤلفون: Nydia Strachman Bacal, Rocio Hassan, Gislaine B. Oliveira, Elvira Deolinda Rodrigues Pereira Velloso, Davi Coe Torres, Roberta Cardoso Petroni, João Renato Rebello Pinho, Roberta Sitnik, Marcela B. Mansur, Irene Lorand-Metze, PV Campregher, Nair Hideko Muto, Nelson Hamerschlak, Cristóvão Luis Pitangueira Mangueira, Flavia Pereira de Carvalho, Carlos S. Chiattone
المصدر: BioMed Research International
BioMed Research International, Vol 2016 (2016)مصطلحات موضوعية: 0301 basic medicine, Male, Article Subject, Chronic lymphocytic leukemia, DNA Mutational Analysis, lcsh:Medicine, Trisomy, Biology, medicine.disease_cause, Polymerase Chain Reaction, General Biochemistry, Genetics and Molecular Biology, law.invention, Cohort Studies, 03 medical and health sciences, Exon, chemistry.chemical_compound, 0302 clinical medicine, INDEL Mutation, Protein Domains, law, hemic and lymphatic diseases, medicine, Humans, Receptor, Notch1, Polymerase chain reaction, Alleles, Mutation, Chromosomes, Human, Pair 12, General Immunology and Microbiology, lcsh:R, General Medicine, medicine.disease, Molecular biology, Leukemia, Lymphocytic, Chronic, B-Cell, Leukemia, 030104 developmental biology, chemistry, 030220 oncology & carcinogenesis, Female, DNA, Research Article
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