Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Elzemar Martins Ribeiro Rodrigues"'
Autor:
Luciana Santos Serrão de Castro, Anderson Nonato do Rosario Marinho, Elzemar Martins Ribeiro Rodrigues, Giorgio Christie Tavares Marques, Tarcísio André Amorim de Carvalho, Luiz Carlos Santana da Silva, Sidney Emanuel Batista dos Santos
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Vol 79, Iss 1, Pp 95-99 (2013)
A deficiência auditiva afeta cerca de 1 em cada 1000 recém-nascidos. Mutações no gene da conexina 26 (GJB2) são as causas mais frequentes de surdez não sindrômica em diferentes populações e é sabido que a mutação delGJB6-D13S1830 em DFNB3
Externí odkaz:
https://doaj.org/article/acc18e3f771e4114b29e6d363be60049
Autor:
Pablo Abdon da Costa Francez, Elzemar Martins Ribeiro Rodrigues, Gleycianne Furtado Frazão, Nathalia Danielly dos Reis Borges, Sidney Emanuel Batista dos Santos
Publikováno v:
Genetics and Molecular Biology, Vol 34, Iss 1, Pp 35-39 (2011)
The allelic frequencies of 12 short tandem repeat loci were obtained from a sample of 307 unrelated individuals living in Macapá, a city in the northern Amazon region, Brazil. These loci are the most commonly used in forensics and paternity testing.
Externí odkaz:
https://doaj.org/article/43c6be994504452f9b08ed4b9d506342
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:
Ney Pereira Carneiro dos Santos, Sidney Santos, Ândrea Kely Campos Ribeiro dos Santos, Elzemar Martins Ribeiro Rodrigues, Luana Gomes Lopes Maciel, João Farias Guerreiro
Publikováno v:
Human Biology. 83:627-636
A panel of Ancestry Informative Markers (AIMs) was used to identify population substructure and estimate individual and overall interethnic admixture in 294 individuals from seven African-derived communities of the Brazilian Amazon. A panel of 48 bia
Autor:
Pablo Abdon da Costa Francez, Afrânio Maurício de Velasco, Sidney Santos, Elzemar Martins Ribeiro Rodrigues
Publikováno v:
International Journal of Legal Medicine. 126:491-496
Insertion-deletion (INDEL) markers are very frequent in the human genome and present several advantages for population and forensic studies, such as low mutation rates, easy interpretation, small amplicons, easy genotyping, and the possibility of usi
Autor:
Elzemar Martins Ribeiro-Rodrigues, Ney Pereira Carneiro dos Santos, Ândrea Ribeiro-dos-Santos, Cecilia Helena Fricke Matte, Marco Antônio Zago, Leonor Gusmão, João Farias Guerreiro, António Amorim, Sidney Santos, Mara H. Hutz, Rui Pereira
Publikováno v:
Human Mutation. 31:184-190
Estimating the proportions of different ancestries in admixed populations is very important in population genetics studies, and it is particularly important for detecting population substructure effects in case-control association studies. In this wo
Publikováno v:
Forensic Science International. 166:233-239
Haplotype and allele frequencies of the nine Y-STR (DYS19, DYS389 I, DYS389 II, DYS390, DYS391, DYS392, DYS393, DYS385 I/II) were determined in a population sample of 200 unrelated males from Belém, Brazil. The most common haplotypes are shared by 1
Autor:
Leonor Gusmão, Sidney Santos, Ândrea Kely Campos Ribeiro dos Santos, Elzemar Martins Ribeiro-Rodrigues, Rui Pereira, Marco Antonio Zago, Ney Pereira Carneiro dos Santos, António Amorim
Publikováno v:
American Journal of Human Biology. 21:707-709
In this study, a PCR multiplex was optimized, allowing the simultaneous analysis of 13 X-chromosome Insertion/deletion polymorphisms (INDELs). Genetic variation observed in Africans, Europeans, and Native Americans reveals high inter-population varia
Autor:
Luiz Carlos Santana da Silva, Elzemar Martins Ribeiro Rodrigues, Giorgio Christie Tavares Marques, Luciana Santos Serrão de Castro, Anderson Nonato do Rosario Marinho, Tarcísio André Amorim de Carvalho, Sidney Santos
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Volume: 79, Issue: 1, Pages: 95-99, Published: FEB 2013
Repositório Institucional da UFPA
Universidade Federal do Pará (UFPA)
instacron:UFPA
Repositório Institucional da UFPA
Universidade Federal do Pará (UFPA)
instacron:UFPA
A deficiência auditiva afeta cerca de 1 em cada 1000 recém-nascidos. Mutações no gene da conexina 26 (GJB2) são as causas mais frequentes de surdez não sindrômica em diferentes populações e é sabido que a mutação delGJB6-D13S1830 em DFNB3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3f9d2f04c718eb20614f6815d86bccc
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1808-86942013000100016&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1808-86942013000100016&lng=en&tlng=en
Autor:
Lilian Kimura, João Pedro Vicente, Sidney Santos, Regina Célia Mingroni-Netto, Elzemar Martins Ribeiro-Rodrigues, Maria Teresa B. M. Auricchio
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Objectives: xMany Africans were brought to Brazil as slaves. The runaway or abandoned slaves founded isolated communities named quilombos. There are many quilombo remnants in Vale do Ribeira region in the southern part of Sao Paulo State. The aim of