Fabio Pinto Silva

Dr. Fabio Pinto Silva

Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil
orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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1 September 2010 in Materials & Design (1980-2015)
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Journal Article
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LBLiciane Sabadin Bertol
Liciane Sabadin Bertol
WJWilson Kindlein Júnior
Wilson Kindlein Júnior
FSFabio Pinto Silva
Fabio Pinto Silva
CAClaus Aumund-Kopp
Claus Aumund-Kopp

22 May 2020 in Science Advances
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Journal Article
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ACAnne-Amandine Chassot
Anne-Amandine Chassot
MRMorgane Le Rolle
Morgane Le Rolle
GJGeneviève Jolivet
Geneviève Jolivet
ISIsabelle Stevant
Isabelle Stevant
JGJean-Marie Guigonis
Jean-Marie Guigonis
MCMarie-Christine Chaboissier
Marie-Christine Chaboissier
In mammals, the timing of meiosis entry is regulated by signals from the gonadal environment. All-trans retinoic acid (ATRA) signaling is considered the key pathway that promotes Stra8 (stimulated by retinoic acid 8) expression and, in turn, meiosis entry. This model, however, is debated because it is based on analyzing the effects of exogenous ATRA on ex vivo gonadal cultures, which not accurately reflects the role of endogenous ATRA. Aldh1a1 and Aldh1a2, two retinaldehyde dehydrogenases synthesizing ATRA, are expressed in the mouse ovaries when meiosis initiates. Contrary to the present view, here, we demonstrate that ATRA-responsive cells are scarce in the ovary. Using three distinct gene deletion models for Aldh1a1;Aldh1a2;Aldh1a3, we show that Stra8 expression is independent of ATRA production by ALDH1A proteins and that germ cells progress through meiosis. Together, these data demonstrate that ATRA signaling is dispensable for instructing meiosis initiation in female germ cells.

16 October 2018 in Rapid Prototyping Journal
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Journal Article
Closed access
JSJuliana Breda Soares
Juliana Breda Soares
JFJoão Finamor
João Finamor
FSFabio Pinto Silva
Fabio Pinto Silva
Liane RoldoLiane Roldo
Liane Roldo
LCLuis Henrique Cândido
Luis Henrique Cândido
Purpose: This paper aims to analyse the effect of different polylactic acid (PLA) colours used on fused deposition modelling (FDM), considering the product finishing quality produced with the same process conditions. Design/methodology/approach: The methodology adopted was to design a virtual modelling object and three-dimensional (3D) print it with FDM with different PLA colours (natural, green and black), using the same parameters. 3D scanning and scanning electron microscopy was used to analyse the model finishing of each sample. Fourier-transform infrared spectroscopy analysis, thermogravimetric analysis and dynamic mechanical analysis were used to characterize the material and verify if the colour affected its thermal behaviour. Findings: Findings showed that different PLA colours lead to distinct 3D printed finishings under the same process conditions. Thermal analysis showed a reason for the printing finishing difference. The degradation temperatures and the glass temperatures vary depending on the PLA colour. This affects the FDM working temperature. Originality/value: This study will contribute to improving the finishing quality of 3D printed products by collaborating to the determination of its process conditions.

25 August 2021 in The EMBO Journal
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Journal Article
Open access
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FSFabio Da Silva
Fabio Da Silva
KZKaiqing Zhang
Kaiqing Zhang
APAnneline Pinson
Anneline Pinson
EFEdoardo Fatti
Edoardo Fatti
MWMichaela Wilsch‐Bräuninger
Michaela Wilsch‐Bräuninger
CNChristof Niehrs
Christof Niehrs
EMBO Press is an editorially independent publishing platform for the development of EMBO scientific publications.

8 October 2021 in eLife
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Journal Article
Open access
FSFabio Da Silva
Fabio Da Silva
FMFariba Jian Motamedi
Fariba Jian Motamedi
LALahiru Chamara Weerasinghe Arachchige
Lahiru Chamara Weerasinghe Arachchige
ATAmelie Tison
Amelie Tison
SBStephen T Bradford
Stephen T Bradford
ASAndreas Schedl
Andreas Schedl
Retinoic acid (RA) is an essential signaling molecule for cardiac development and plays a protective role in the heart after myocardial infarction (MI). In both cases, the effect of RA signaling on cardiomyocytes, the principle cell type of the heart, has been reported to be indirect. Here we have developed an inducible murine transgenic RA-reporter line using CreERT2 technology that permits lineage tracing of RA-responsive cells and faithfully recapitulates endogenous RA activity in multiple organs during embryonic development. Strikingly, we have observed a direct RA response in cardiomyocytes during mid-late gestation and after MI. Ablation of RA signaling through deletion of the Aldh1a1/a2/a3 genes encoding RA-synthesizing enzymes leads to increased cardiomyocyte apoptosis in adults subjected to MI. RNA sequencing analysis reveals Tgm2 and Ace1, two genes with well-established links to cardiac repair, as potential targets of RA signaling in primary cardiomyocytes, thereby providing novel links between the RA pathway and heart disease.

1 November 2014 in Wear
Verified
Journal Article
Closed access
PNP.D. Neis
P.D. Neis
NFNey Francisco Ferreira
Ney Francisco Ferreira
FSFabio Pinto Silva
Fabio Pinto Silva