Gustavo Satoru Kajitani

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-|Bsc,<b>Biological Sciences</b>, <b>Universidade de São Paulo ISP</b>, 2013 <br>Has experience in In vivo research, Cell Biology, Molecular Biology, Neuroinflammation, and DNA repair deficiencies<br> Gustavo Satoru is a <b>PhD student</b> in the DNA Repair Lab - <b>Institute of Biomedical Sciences</b> at <b>University of Sao Paulo</b> since 2013, having spent one year of his PhD as a <b>visiting scientist</b> in the [https://www.hsph.harvard.edu/james-mitchell/gustavo-satoru-kajitani/ Mitchell Lab] - <b>Harvard T.H. Chan School of Public Health</b>.<br><br>Research keywords: <b>DNA Repair</b>, <b> Photolesions</b>,<b>Aging and Inflammation</b>.<br><br>[http://buscatextual.cnpq.br/buscatextual/visualizacv.do?metodo=apresentar&id=K4331588Z6 Lattes] <br> Contato: gustkajitani[at]gmail.com+|Bsc,<b>Biological Sciences</b>, <b>Universidade de São Paulo ISP</b>, 2013 <br>Has experience in In vivo research, Cell Biology, Molecular Biology, Neuroinflammation, and DNA repair deficiencies<br><br> Gustavo Satoru is a <b>PhD student</b> in the DNA Repair Lab - <b>Institute of Biomedical Sciences</b> at <b>University of Sao Paulo</b> since 2013, having spent one year of his PhD as a <b>visiting scientist</b> in the [https://www.hsph.harvard.edu/james-mitchell/gustavo-satoru-kajitani/ Mitchell Lab] - <b>Harvard T.H. Chan School of Public Health</b>.<br><br>Research keywords: <b>DNA Repair</b>, <b> Photolesions</b>,<b>Aging and Inflammation</b>.<br><br>[http://buscatextual.cnpq.br/buscatextual/visualizacv.do?metodo=apresentar&id=K4331588Z6 Lattes] <br> Contato: gustkajitani[at]gmail.com
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Revisão de 18:07, 25 Abril 2018

Bsc,Biological Sciences, Universidade de São Paulo ISP, 2013
Has experience in In vivo research, Cell Biology, Molecular Biology, Neuroinflammation, and DNA repair deficiencies

Gustavo Satoru is a PhD student in the DNA Repair Lab - Institute of Biomedical Sciences at University of Sao Paulo since 2013, having spent one year of his PhD as a visiting scientist in the Mitchell Lab - Harvard T.H. Chan School of Public Health.

Research keywords: DNA Repair, Photolesions,Aging and Inflammation.

Lattes
Contato: gustkajitani[at]gmail.com



Current Project

Effects of DNA lesions on Nucleotide Excision Repair deficient mice

The Nucleotide Excision Repair (NER) pathway is responsible for the removal and repair of bulky DNA lesions capable of distorting the structure of the DNA double helix, such as cisplatin or UV induced lesions. Defects in genes related to the Nucleotide Excision Repair (NER) pathway lead to disorders in which patients display photosensitivity and/or neurological problems, such as Xeroderma Pigmentosum (XP), Cockayne Syndrome (CS). In order to study the impact of DNA damage in these genetic diseases, numerous knockout mice models have been developed, with several of them having similar characteristics to the human syndromes. In this project, we aim to study the impact of specific UV induced lesions (CPDs or 6-4PPs) on the induction of effects such as skin hyperplasia, cell death and inflammation on a XP mouse model. Moreover, we have used a Cockayne Syndrome mouse model in order to study the relationship between the molecular defects of CS and possible neuropathological phenotypes, namely vascular dysfunction and neuroinflammation.

Publications

Ferramentas pessoais