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Silvia Regina Rogatto

Researcher at University of Southern Denmark

Publications -  205
Citations -  3773

Silvia Regina Rogatto is an academic researcher from University of Southern Denmark. The author has contributed to research in topics: Cancer & Gene. The author has an hindex of 30, co-authored 189 publications receiving 3135 citations. Previous affiliations of Silvia Regina Rogatto include National Institute of Standards and Technology & AC Camargo Hospital.

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CDH1 promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer.

TL;DR: The preliminary findings suggested that abnormal CDH1 methylation occurs in high frequencies in infiltrating breast cancers associated with a decrease in E-cadherin expression in a subgroup of cases characterized by loss of expression of other important genes to the mammary carcinogenesis process, probably due to the disruption of the mechanism of maintenance of DNA methylation in tumoral cells.
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The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome

Anamaria A. Camargo, +99 more
TL;DR: Open reading frame expressed sequences tags (ORESTES) as discussed by the authors differ from conventional ESTs by providing sequence data from the central protein coding portion of transcripts, which can be used for gene discovery and shotgun transcript sequence generation.
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Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags

Sandro J. de Souza, +78 more
TL;DR: A set of 250,000 cDNAs that represent partial expressed gene sequences and that are biased toward the central coding regions of the resulting transcripts, termed ORF expressed sequence tags (ORESTES), defined 48 transcribed sequences on chromosome 22 not defined by other sequences.
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An Inherited Small Microdeletion at 15q13.3 in a Patient with Early- Onset Obsessive-Compulsive Disorder

TL;DR: A pilot genome-wide screen for CNVs in a cohort of patients with early-onset obsessive-compulsive disorder and 12 mentally healthy individuals found a small rare paternal inherited microdeletion in one male patient with very early onset OCD, which supports the hypothesis of a complex network of several genes expressed in the brain contributing for the genetic risk of OCD.