9 results match your criteria: "UPorto - University of Porto[Affiliation]"
Front Cell Dev Biol
November 2024
Molecular Genetics Laboratory, Laboratory Genetics Service, Genetics and Pathology Clinic, Centro Hospitalar Universitário de Santo António, Unidade Local de Saúde de Santo António, Porto, Portugal.
Reprod Biol Endocrinol
June 2024
Molecular Genetics Laboratory, Laboratory Genetics Service, Genetics and Pathology Clinic, Unidade Local de Saúde de Santo António (ULSSA), Porto, Portugal.
Background: Premutations in the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene, defined as between 55 and 200 CGGs, have been implicated in fragile X-associated primary ovarian insufficiency (FXPOI). Only 20% of female premutation carriers develop early ovulatory dysfunction, the reason for this incomplete penetrance is unknown. This study validated the mathematical model in premutation alleles, after assigning each allele a score representing allelic complexity.
View Article and Find Full Text PDFMicrosc Res Tech
July 2019
Laboratory of Histology and Embryology, Department of Microscopy, ICBAS - Institute of Biomedical Sciences Abel Salazar, UPorto - University of Porto, Porto, Portugal.
The main intent of this work (after the by chance finding, in archived histological slides) is to characterize one previously non-described liver lesion of the Iberian barbel from the Vizela River (Portugal). This ran through a textile and dyeing industrial region. The lesion type was made of groups of foamy cells (presumptive macrophages), which appear either as a "smaller non-nodular form," without a connective tissue capsule and displaying an irregular profile, or as a "bigger nodular form," presenting a thin capsule and a circular profile.
View Article and Find Full Text PDFPLoS One
May 2016
CIIMAR, Interdisciplinary Centre of Marine and Environmental Research, CIMAR Associate Laboratory, UPorto-University of Porto, Porto, Portugal; Department of Biology, Faculty of Sciences, University of Porto, Porto, Portugal.
The Carnitine palmitoyltransferase I (Cpt1) gene family plays a crucial role in energy homeostasis since it is required for the occurrence of fatty acid β-oxidation in the mitochondria. The exact gene repertoire in different vertebrate lineages is variable. Presently, four genes are documented: Cpt1a, also known as Cpt1a1, Cpt1a2; Cpt1b and Cpt1c.
View Article and Find Full Text PDFReprod Fertil Dev
October 2016
CIIMAR - Interdisciplinary Centre of Marine and Environmental Research, CIMAR Associated Laboratory, UPorto - University of Porto, Laboratory of Cellular, Molecular and Analytical Studies, Rua dos Bragas 289, 4050-123 Porto, Portugal.
The basic pathway of oocyte development and its regulation is evolutionarily conserved among vertebrates; however, little is known about the role of hormones at the first stages (Stages I and II) of follicle development in fish. In the present study, zebrafish follicles at Stages I and II were exposed in vitro to the reproductive hormones 17β-oestradiol (E), 11-ketotestosterone (11KT), 17,20β-dihydroxy-4-pregnen-3-one (DHP) and to the secondary messenger dibutyryl cyclic adenosine monophosphate (db-cAMP) at a concentration of 1µM for a 48-h period. Morphological alterations of the ooplasm were assessed by transmission electron microscopy and of the granulosa cell layer by quantitative stereology.
View Article and Find Full Text PDFGenome Biol Evol
December 2014
CIIMAR-Interdisciplinary Centre of Marine and Environmental Research, CIMAR Associate Laboratory, UPorto-University of Porto, Portugal Department of Biology, Faculty of Sciences, UPorto-University of Porto, Portugal
The uptake and transport of vitamin B12 (cobalamin; Cbl) in mammals involves a refined system with three evolutionarily related transporters: transcobalamin 1 (Tcn1), transcobalamin 2 (Tcn2), and the gastric intrinsic factor (Gif). Teleosts have a single documented binder with intermediate features to the human counterparts. Consequently, it has been proposed that the expansion of Cbl binders occurred after the separation of Actinopterygians.
View Article and Find Full Text PDFComp Biochem Physiol A Mol Integr Physiol
January 2013
CIIMAR - Interdisciplinary Centre of Marine and Environmental Research, CIMAR Associate Laboratory, UPorto - University of Porto, Laboratory of Cellular, Molecular and Analytical Studies, Rua dos Bragas 289, 4050-123 Porto, Portugal.
A negative correlation between female gonadal maturation kinetics and size variations of hepatic peroxisomes was earlier documented in brown trout, as a probable impact of serum estrogen changes during the reproductive cycle. Herein, we investigated whether the organelle volume/surface dynamics seen in female brown trout liver peroxisomes - without numerical changes within each hepatocyte - is followed by variations in the expression of the membrane peroxisome protein Pex11α gene. For comparison, we also studied males.
View Article and Find Full Text PDFPLoS One
August 2012
CIMAR Associate Laboratory, CIIMAR-Interdisciplinary Centre of Marine and Environmental Research, UPorto-University of Porto, Porto, Portugal.
Background: Aspartic proteases comprise a large group of enzymes involved in peptide proteolysis. This collection includes prominent enzymes globally categorized as pepsins, which are derived from pepsinogen precursors. Pepsins are involved in gastric digestion, a hallmark of vertebrate physiology.
View Article and Find Full Text PDFComp Biochem Physiol B Biochem Mol Biol
June 2009
CIIMAR - Interdisciplinary Centre of Marine and Environmental Research, CIMAR Associate Laboratory, UPorto - University of Porto, Laboratory of Cellular, Molecular and Analytical Studies, Rua dos Bragas 289, 4050-123 Porto, Portugal.
Previously, it was documented that liver peroxisomes display seasonal size changes in the adult Salmo trutta fario, especially in females (and negatively correlated with ovary maturation). It was then hypothesized that decreases in peroxisome size could be paralleled by changes in peroxisomal beta-oxidation and estradiol catabolism actions. The 17beta-hydroxysteroid dehydrogenase 4 has been portrayed as playing an important role in both processes.
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