Brazilian industrial yeasts show high fermentative performance in high solids content for corn ethanol process

Autor: Thaís O. Secches, Carla F. Santos Viera, Thaynara K. E. Pereira, Victor T. O. Santos, Jade Ribeirodos Santos, Gonçalo A. G. Pereira, Marcelo F. Carazzolle

Publikováno v: Bioresources and Bioprocessing, Vol 9, Iss 1, Pp 1-9 (2022)

Abstract An imminent change in the world energy matrix makes it necessary to increase the production of renewable fuels. The United States and Brazil are the world's largest producers, but their production methods are very different, using different

Externí odkaz: https://doaj.org/article/f90155e0a2a04bb3b4bbfb99a963ce99

A candidate vaccine for human visceral leishmaniasis based on a specific T cell epitope-containing chimeric protein protects mice against

Autor: Daniela P, Lage, Patrícia A F, Ribeiro, Daniel S, Dias, Débora V C, Mendonça, Fernanda F, Ramos, Lívia M, Carvalho, Daysiane, de Oliveira, Bethina T, Steiner, Vívian T, Martins, Luísa, Perin, Amanda S, Machado, Thaís T O, Santos, Grasiele S V, Tavares, João A, Oliveira-da-Silva, Jamil S, Oliveira, Bruno M, Roatt, Ricardo A, Machado-de-Ávila, Antônio L, Teixeira, Maria V, Humbert, Eduardo A F, Coelho, Myron, Christodoulides

Publikováno v: NPJ Vaccines

Leishmaniases are neglected diseases caused by infection with Leishmania parasites and there are currently no prophylactic vaccines. In this study, we designed in silico a synthetic recombinant vaccine against visceral leishmaniasis (VL) called Chime

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0c3f8cc034066e203c6b63b6ed2ae782
https://pubmed.ncbi.nlm.nih.gov/32821440

Mutational characterization of the P3H1/CRTAP/CypB complex in recessive osteogenesis imperfecta

Autor: M R G O Rebouças, V. Sipolatti, Maira Trancozo, M.G. Almeida, L S Almeida, V R R Nunes, Clara Barbirato, J C G Duarte, Flavia de Paula, T O Santos

Publikováno v: Genetics and Molecular Research. 14:15848-15858

Osteogenesis imperfecta (OI) is a genetic disease characterized by bone deformities and fractures. Most cases are caused by autosomal dominant mutations in the type I collagen genes COL1A1 and COL1A2; however, an increasing number of recessive mutati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e7d21f6f655ed2ebe476cdcace0d4f6
https://doi.org/10.4238/2015.december.1.36

Multipredictive adaptive control of arc welding trailing centerline temperature

Autor: F. J. Coito, T. O. Santos, R.B. Caetano, João M. Lemos

Publikováno v: ResearcherID
CIÊNCIAVITAE

This application paper addresses the use of adaptive predictive control on arc welding trailing centerline temperature control. For tackling the high level of uncertainty in the process the multivariable multipredictive adaptive regulator (MUSMAR) ad

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7323c2b7a2c2d92e060605b2f54a0042
https://doi.org/10.1109/87.817701

Griscelli syndrome-type 2 in twin siblings: case report and update on RAB27A human mutations and gene structure

Autor: T C Izidoro-Toledo, J Gurgel-Gianetti, T O Santos, Enilza Maria Espreáfico, I. P. Meschede

Publikováno v: Brazilian Journal of Medical and Biological Research v.41 n.10 2008
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Vol 41, Iss 10, Pp 839-848 (2008)
Brazilian Journal of Medical and Biological Research, Volume: 41, Issue: 10, Pages: 839-848, Published: OCT 2008

Griscelli syndrome (GS) is a rare autosomal recessive disorder caused by mutation in the MYO5A (GS1, Elejalde), RAB27A (GS2) or MLPH (GS3) genes. Typical features of all three subtypes of this disease include pigmentary dilution of the hair and skin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d4fb3f6e3bdede832ee49b7401ca371
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2008001000002