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of 8
pro vyhledávání: '"Carlos Henrique Ares Silveira, da Motta"'
Autor:
Elvira Deolinda Rodrigues Pereira Velloso, Carlos Henrique Ares Silveira da Motta, Juliana Braga Furtado, Nydia Strachman Bacal, Paulo Augusto Achucarro Silveira, Cynthia Bachir Moyses, Roberta Sitnik, João Renato Rebello Pinho
Publikováno v:
Einstein (São Paulo), Vol 9, Iss 2, Pp 184-189 (2011)
Objective: To study the frequency of mutations that may lead to a good or bad prognosis, as well as their relation with the karyotype and immunophenotype in patients with acute myeloid leukemia. Methods: Thirty samples of patients with acute myeloid
Externí odkaz:
https://doaj.org/article/56e0bc200ee74f3da09800dfaf3e90c6
Autor:
Carlos Henrique Ares Silveira da Motta, Clarice Sampaio Alho, Ana Paula Magalhães Leboute, Fernanda Irma Remus Hamester, Débora Santos da Silva
Publikováno v:
ELECTROPHORESIS. 40:2873-2876
Well-defined estimates of mutation rates in highly polymorphic tetranucleotide STR loci are a prerequisite for human identification in genetics laboratory routines useful for civil and criminal investigations. Studying 15 autosomal STR loci of forens
Autor:
Carlos Henrique Ares Silveira da Motta, André Zoratto Gastaldo, C.P. Cavalheiro, Rodrigo Rodenbusch, Clarice Sampaio Alho, Eduardo Avila, Pietra Graebin
Publikováno v:
Forensic Science International: Genetics. 49:102368
Considering the overall frequency of paternity investigation cases including mutational events, there is a real possibility that at least a fraction of all inconsistencies reported in paternity cases are caused not by polymerase slippage mutations, b
Autor:
Ilíada Rainha de Souza, Giovanna C Cavalcante, Dayse A. Silva, Sidney Santos, Gustavo Chemale, Andrea Rita Marrero, Renato T.F. Paranaiba, Mirella Perruccio Soler, Carlos Henrique Ares Silveira da Motta, Elzemar Martins Ribeiro Rodrigues, Daniela Koshikene, Teresinha de Jesus Brabo Ferreira Palha, Lídia Alexandre, Clineu Julien Seki Uehara, Elizeu Fagundes de Carvalho, Jorge Marcelo de Freitas
Publikováno v:
Forensic Science International: Genetics. 19:10-14
The aim of this study was to estimate the diversity of 30 insertion/deletion (INDEL) markers (Investigator(®) DIPplex kit) in a sample of 519 individuals from six Brazilian states and to evaluate their applicability in forensic genetics. All INDEL m
Autor:
Paulo Eduardo Raimann, Adelar Mantovani, Laiana Silveira Beltrami, Tatiana Lúcia Santos Nogueira, Thaty Fumiko Mishima, Cinthia Bachir Moysés, Carlos Henrique Ares Silveira da Motta, Sandra Maria dos Santos, Ian Marques Cândido, Weslley Mottoi Tsutsumida, Leonor Gusmão, Carlos Antonio de Souza, Bruno Boiko Pereira de Figueiredo, Rochele Kovalski Lopes, Olívia Cristina Lima dos Santos, Neide Maria de Oliveira Godinho, Altamir Frederico Guidolin
Publikováno v:
Forensic Science International: Genetics. 26:e28-e30
Publikováno v:
International journal of legal medicine. 133(1)
A sample of 158 Brazilian males from Sao Paulo (SP), Brazilian southeast, was typed for 17 Y-STR loci (DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393, DYS437, DYS438, DYS439, DYS448, DYS456, DYS458, DYS635, YGATA_H4.1, and DYS385ab). A tota
Autor:
Cinthia Bachir, Moysés, Weslley Mottoi, Tsutsumida, Paulo Eduardo, Raimann, Carlos Henrique Ares Silveira, da Motta, Tatiana Lúcia Santos, Nogueira, Olívia Cristina Lima, Dos Santos, Bruno Boiko Pereira, de Figueiredo, Thaty Fumiko, Mishima, Ian Marques, Cândido, Neide Maria, de Oliveira Godinho, Laiana Silveira, Beltrami, Rochele Kovalski, Lopes, Altamir Frederico, Guidolin, Adelar, Mantovani, Sandra Maria, Dos Santos, Carlos Antonio, de Souza, Leonor, Gusmão
Publikováno v:
Forensic science international. Genetics. 26
Autor:
Leonor Gusmão, Rodrigo Rodenbusch, Juliane Bentes Picanço, Clarice Sampaio Alho, Carlos Henrique Ares Silveira da Motta, Paulo Eduardo Raimann
Publikováno v:
Forensic science international. Genetics. 16
Genotyping of polymorphic short tandem repeats (STRs) loci is widely used in forensic DNA analysis. STR loci eventually present tri-allelic pattern as a genotyping irregularity and, in that situation, the doubt about the tri-allele locus frequency ca