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Fulvio Gandolfi

Researcher at University of Milan

Publications -  216
Citations -  7092

Fulvio Gandolfi is an academic researcher from University of Milan. The author has contributed to research in topics: Embryonic stem cell & Oocyte. The author has an hindex of 47, co-authored 203 publications receiving 6598 citations. Previous affiliations of Fulvio Gandolfi include University of Rome Tor Vergata.

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Changes in poly(A) tail length of maternal transcripts during in vitro maturation of bovine oocytes and their relation with developmental competence.

TL;DR: Most of the examined transcripts follow the default deadenylation pattern described during oocyte maturation in other species and that a shorter poly(A) tail is correlated with low developmental competence.
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Brief demethylation step allows the conversion of adult human skin fibroblasts into insulin-secreting cells

TL;DR: This work shows that it is possible to convert adult fibroblasts into insulin-secreting cells, avoiding both a stable pluripotent stage and any transgenic modification.
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Comparative analysis of calf and cow oocytes during in vitro maturation

TL;DR: To determine possible causes of reported differences between developmental competence of oocytes isolated from prepubertal calves and adult cows, three parameters were analysed, comparatively, during in vitro maturation (IVM): oocyte diameter, oocyte energy metabolism, and protein synthesis of oocyte and cumulus cells.
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Effect of different levels of intracellular cAMP on the in vitro maturation of cattle oocytes and their subsequent development following in vitro fertilization.

TL;DR: It is concluded that the maintenance of an optimal intracellular concentration of cAMP before and during IVM ensures a high developmental competence of bovine oocytes matured in medium without serum and hormones.
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Porcine embryonic stem cells: Facts, challenges and hopes

TL;DR: Data from the literature will be presented together with experimental evidence recently obtained in the laboratory and aspects related to the timing of isolation, the initiation of primary cultures, the use of different culture conditions and cytokines, the identification of pluripotency-related molecular markers in the pig will be examined.