Abstract
Administer the share of technical reserves for costs of institutional infrastructure for Research on Exercise 2019. This project aims to improve the infrastructure of common use CBMEG and maintenance equipment. (AU)
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Edi Lúcia Sartorato
CV Lattes
ResearcherID
ORCID
Universidade Estadual de Campinas (UNICAMP). Centro de Biologia Molecular e Engenharia Genética (CBMEG) (Institutional affiliation from the last research proposal) Birthplace: Brazil
graduate at Química from Universidade Estadual de Campinas (1989), master's at Genetics from Universidade Estadual de Campinas (1994) and ph.d. at Genetics from Universidade Estadual de Campinas (1997). Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: surdez, conexina, mutação, genética and conexina 26. (Source: Lattes Curriculum)
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Research grants
- Infrastructure Costs of Institutional Research - Year 2019., AP.RT.INST
- Infrastructure Costs of Institutional Research - Year 2017., AP.RT.INST
Abstract
Administer the share of technical reserves for costs of institutional infrastructure for Research on Exercise 2017. This project aims to improve the infrastructure of common use CBMEG and maintenance equipment. (AU)
- Molecular and functional study of Usher's syndrome using massive sequencing, zebrafish and CRISPR/Cas9 system, AP.R
Abstract
Usher syndrome is an autosomal recessive hereditary disease characterized by hearing loss and progressive loss of vision. Vision loss occurs due to retinitis pigmentosa, a degenerative retinal disease that usually appears in adolescence or early adulthood. A global molecular diagnostic protocol for Usher's syndrome has been difficult because of the high genetic heterogeneity, large number…
(Only some records are available in English at this moment)
Scholarships in Brazil
- Screening of genetic variants of Ménière's disease, BP.IC
Abstract
Ménière's disease (DM) is the second most common labyrinth disease in Brazil. It is characterized by the presence of symptomatic tetrad: vertigo, hearing loss, tinnitus and aural fullness. It can occur at any age, being more frequent in adults between 30-50 years and less common in children and young adults. The incidence varies depending on the geographical region and ethnic group, howev…
- Deep sequencing for identification and characterization of deafness genes, BP.DR
Abstract
Hearing loss is the most common sensory impairment in humans, affecting approximately 10% of the entire world population. The restriction of communication by oral expression results in changes in cognitive and psychological development of the affected individual. In developed countries, one in every 500 individuals has profound/severe bilateral sensorineural hearing loss. In cases of indi…
- Study of genetic etiology of deafness in newborn at risk, BP.IC
Scholarships abroad
- Deep sequencing to identify and characterize deafness genes, BE.EP.DR
Abstract
Hearing loss is the most common sensory impairment in humans, affecting approximately 10% of the entire world population. The restriction of communication by oral expression results in changes in cognitive and psychological development of the affected individual. In developed countries, one in every 500 individuals has profound/severe bilateral sensorineural hearing loss. Among the causes…
Total / Available in English
| 40 / 22 | Completed research grants |
| 33 / 3 | Completed scholarships in Brazil |
| 1 / 1 | Completed scholarships abroad |
| 74 / 26 | All research grants and scholarships |
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