Leonardo Rocha Vidal Ramos

Dr. Leonardo Rocha Vidal Ramos

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Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 May 2020 in Aquaculture Research
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GHGuilherme Melgaço Heluy
Guilherme Melgaço Heluy
LRLeonardo Rocha Vidal Ramos
Leonardo Rocha Vidal Ramos
VPVirgínia Fonseca Pedrosa
Virgínia Fonseca Pedrosa
CSCristiane Sarturi
Cristiane Sarturi
PFPaulo Gustavo Pires Figueiredo
Paulo Gustavo Pires Figueiredo
MPMarcelo Maia Pereira
Marcelo Maia Pereira

1 July 2015 in Animal Feed Science and Technology
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Journal Article
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LRLeonardo Rocha Vidal Ramos
Leonardo Rocha Vidal Ramos
LRLuis Alberto Romano
Luis Alberto Romano
José María MonserratJosé María Monserrat
José María Monserrat
PAP.C. Abreu
P.C. Abreu
PVP.E. Verde
P.E. Verde
Marcelo Borges TesserMarcelo Borges Tesser
Marcelo Borges Tesser

14 September 2017 in Journal of Fish Biology
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MOM. C. L. M. Oliveira
M. C. L. M. Oliveira
RMR. Mont'Alverne
R. Mont'Alverne
LSLuis Andre Sampaio
Luis Andre Sampaio
Marcelo Borges TesserMarcelo Borges Tesser
Marcelo Borges Tesser
LRLeonardo Rocha Vidal Ramos
Leonardo Rocha Vidal Ramos
AGA. M. Garcia
A. M. Garcia

1 January 2017 in Genetics and Molecular Research
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Journal Article
Open access
JRJ Riet
J Riet
LRLeonardo Rocha Vidal Ramos
Leonardo Rocha Vidal Ramos
RLR V Lewis
R V Lewis
LML F Marins
L F Marins
Although PCR-based techniques have become an essential tool in the field of molecular and genetic research, the amplification of repetitive DNA sequences is limited. This is due to the truncated nature of the amplified sequences, which are also prone to errors during DNA polymerase-based amplification. The complex structure of repetitive DNA can form hairpin loops, which promote dissociation of the polymerase from the template, impairing complete amplification, and leading to the formation of incomplete fragments that serve as megaprimers. These megaprimers anneal with other sequences, generating unexpected fragments in each PCR cycle. Our gene model, MaSp1, is 1037-bp long, with 68% GC content, and its amino acid sequence is characterized by poly-alanine-glycine motifs, which represent the repetitive codon consensus. We describe the amplification of the MaSp1 gene through minor changes in the PCR program. The results show that a denaturation temperature of 98°C is the key determinant in the amplification of the MaSp1 partial gene sequence.

9 February 2017 in Anais da Academia Brasileira de Ciências
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LRLeonardo Rocha Vidal Ramos
Leonardo Rocha Vidal Ramos
VPVirgínia F. Pedrosa
Virgínia F. Pedrosa
AMAgnes Mori
Agnes Mori
CACarlos F.F. DE Andrade
Carlos F.F. DE Andrade
LRLuis Alberto Romano
Luis Alberto Romano
Marcelo Borges TesserMarcelo Borges Tesser
Marcelo Borges Tesser
Four soybean meal-based diets containing increasing levels of an enzyme complex (E50, E100, E150 and E200 at 50, 100, 150 and 200 g ton-1, respectively) and one soybean meal-based diet without the enzyme complex (E0) were fed in triplicate to M. liza juveniles in a semi-static flow system with 20 fish per tank for 75 days. There were no differences between the treatments for animal performance parameters, but fish fed the enzyme complex treatment exhibited significantly (P<0.05) higher values of calcium bone retention compared with control fish. Although there was no relationship between bacterial counts in different sections of the gastrointestinal tract or enzyme levels, filamentous bacteria were increased in E50 compared with E150. All of the treatments resulted in higher bacterial counts in the stomach than in intestinal segments. Histological screening showed serious to moderate infiltration of inflammatory cells, modification in villus morphology and necrosis in some cases in fish fed the E0 diet. In addition, fish from the E0 treatment exhibited significantly (P<0.05) lower lipid deposition in the peritoneal cavity. Therefore, the use of low levels of exogenous enzyme is recommended in diets for M. liza when soybean meal is used as the main source of protein.