Zobrazeno 1 - 10 of 26 pro vyhledávání: '"Sylvia Satomi Takeno"'
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Association between PSCA, TNF-α, PARP1 and TP53 Gene Polymorphisms and Gastric Cancer Susceptibility in the Brazilian Population
Autor: Carlos Alberto Malheiros, Eleonidas Moura Lima, Paulo Kassab, Roberto Nery Dantas, Sylvia Satomi Takeno Herrero, Augusto Monteiro de Souza
Publikováno v: Asian Pacific Journal of Cancer Prevention : APJCP
Objectives: To evaluate the association of allelic and genotypic frequencies of PSCA (rs2976392), TNF-α (rs1800629), PARP1 (rs1136410) and TP53 (rs368771578) SNPs with GC susceptibility in a Brazilian population. Materials and Methods: This is a ret
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d4ebc194f78e81c8012a85843967fb0
https://doi.org/10.31557/apjcp.2020.21.1.43
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3
Association of single nucleotide polymorphisms rs63751445 of the MSH2 gene and rs863224614 of the MSH6 gene with susceptibility to breast cancer in samples from Northeast Brazil
Autor: Eleonidas Moura Lima, Agnaldo Luiz do Nascimento, Poliane da Silva Calixto, Evaldo Hipólito de Oliveira, Augusto Monteiro de Souza, Maria Isabela Ferreira de Araújo, Leonardo Ferreira Soares, Maria do Socorro Viana do Nascimento, João Ricardo Gonçalves de Oliveira, Sylvia Satomi Takeno Herrero, Mayara Dos Santos Maia
Publikováno v: Research, Society and Development; Vol. 9 No. 9; e368997007
Research, Society and Development; Vol. 9 Núm. 9; e368997007
Research, Society and Development; v. 9 n. 9; e368997007
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development, Vol 9, Iss 9 (2020)
Breast cancer (BC) is the cancer with the greatest epidemiological impact on the female population worldwide. The disease has a multifactorial etiology, with genetic implications that are not fully understood. In this context, genetic changes in the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4deeb013fac6cc3534c19694b3e10486
https://doi.org/10.33448/rsd-v9i9.7007
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4
Intellectual, adaptive and behavioural characteristics in four patients with 18p deletion syndrome
Autor: Vera Ayres Meloni, Maria Isabel Melaragno, O.F.A. Bueno, Claudia Berlim de Mello, L S E Pimenta, L. M. Benedetto, Sylvia Satomi Takeno
Publikováno v: Journal of Intellectual Disability Research.
BACKGROUND The association of behavioural phenotype assessment with cytogenomic characterisation may provide a better comprehension of genotype-phenotype correlations in syndromes caused by chromosomal abnormalities, such as 18p deletion syndrome. ME
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c064068f3d3d2f378d4c09e95c054018
https://doi.org/10.1111/jir.12568
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6
19q13.33→qter trisomy in a girl with intellectual impairment and seizures
Autor: Vera Ayres Meloni, M. C. M. Oliveira, Sylvia Satomi Takeno, Fernanda Teresa de Lima, Maria Isabel Melaragno, Gianna Carvalheira
Publikováno v: Meta Gene
Rearrangements in chromosome 19 are rare. Among the 35 patients with partial 19q trisomy described, only six have a breakpoint defined by array. The 19q duplication results in a variable phenotype, including dysmorphisms, intellectual disability and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::606cdf5499779e98eb74f2cfc378c439
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8
First Report of a Small Supernumerary der(8;14) Marker Chromosome
Autor: Leslie Domenici Kulikowski, Maria Isabel Melaragno, Roberta Santos Guilherme, Sylvia Satomi Takeno, Ana B. Alvarez Perez, Ahmed B. Hamid, M.M. Oliveira, Elisabeth Klein, Thomas Liehr, A.R.N. Dutra
Publikováno v: Cytogenetic and Genome Research. 139:284-288
Small supernumerary marker chromosomes (sSMC) are structurally abnormal chromosomes, generally equal in size or smaller than a chromosome 20 of the same metaphase spread. Most of them are unexpectedly detected in routine karyotype analyses, and it is
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::054d1f547eb8024ad1afeee973026e0f
https://doi.org/10.1159/000348743
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9
Interstitial 4q Deletion and Isodicentric Y-Chromosome in a Patient with Dysmorphic Features
Autor: R.M. Minillo, Sylvia Satomi Takeno, Maria Isabel Melaragno, Tatiane I. Mancini, M.M. Oliveira, Ana Beatriz Alvarez Perez, A.R.N. Dutra
Publikováno v: Molecular Syndromology. 3:39-43
We present a 2-year-old boy with a de novo 46,XY,idic(Y)(q11.221),del(4)(q26q31.1) karyotype. G-banding, FISH, MLPA, and SNP-array techniques were used to characterize the 24-Mb deletion in 4q and the breakpoint in the isodicentric Y-chromosome regio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea93c519c14ce57268e97f17b776a2b0
https://doi.org/10.1159/000338468
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10
Clinical, Cytogenetic and Molecular Study in a Case of r(3) with 3p Deletion and Review of the Literature
Autor: Silvia Bragagnolo, G.M. Carvolheira, L. Domenici Kulikowski, Denise Maria Christofolini, Sylvia Satomi Takeno, R. Santos Guilherme, Maria Isabel Melaragno, Renata Pellegrino
Publikováno v: Cytogenetic and Genome Research. 134:325-330
Ring chromosome 3 is a rare abnormality with only 10 patients described in the literature. We report a patient with r(3) and ∼6-Mb distal 3p deletion. Single nucleotide polymorphism array, multiplex ligation-dependent probe amplification and fluore
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf69390c2e99c41aba52ea0307d22587
https://doi.org/10.1159/000329478
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