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Ivana Antonucci

Showing results (1-10 of 75) with videos related to

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Asian Journal of Andrology|July 28, 2022
The role of <i>CFTR</i> p.G970D missense mutation in male infertilityIvana Antonucci, Ilaria Angilletta, Federico Anaclerio
Brain Circulation|October 18, 2019
Activity of p53 in human amniotic fluid stem cells increases their potentiality as a candidate for stem cell therapyBlaise Cozene, Ivana Antonucci, Liborio Stuppia
Brain Circulation|October 3, 2018
Amniotic fluid stem cell models: A tool for filling the gaps in knowledge for human genetic diseasesIvana Antonucci, Marci G Crowley, Liborio Stuppia
International Journal of Molecular Sciences|April 11, 2012
Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseasesLiborio Stuppia, Ivana Antonucci, Giandomenico Palka, et al.
Fertility and Sterility|February 17, 2017
Male factor infertility and lack of openness about infertility as risk factors for depressive symptoms in males undergoing assisted reproductive technology treatment in ItalyAlessandra Babore, Liborio Stuppia, Carmen Trumello, et al.
Biomedicines|January 8, 2025
Microbiota and Autism: A Review on Oral and Gut Microbiome Analysis Through 16S rRNA SequencingFederico Anaclerio, Maria Minelli, Ivana Antonucci, et al.
Clinical Epigenetics|November 14, 2015
Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime healthLiborio Stuppia, Marica Franzago, Patrizia Ballerini, et al.
Haematologica|January 19, 2007
Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cellsAlessia Colosimo, Valentina Guida, Ivana Antonucci, et al.
Asian Journal of Andrology|July 27, 2010
Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocolsRossella Giuliani, Ivana Antonucci, Isabella Torrente, et al.
Clinical Case Reports|March 8, 2017
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancerIvana Antonucci, Martina Provenzano, Luca Sorino, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Asian Journal of Andrology|July 28, 2022
The role of <i>CFTR</i> p.G970D missense mutation in male infertilityIvana Antonucci, Ilaria Angilletta, Federico Anaclerio
Brain Circulation|October 18, 2019
Activity of p53 in human amniotic fluid stem cells increases their potentiality as a candidate for stem cell therapyBlaise Cozene, Ivana Antonucci, Liborio Stuppia
Brain Circulation|October 3, 2018
Amniotic fluid stem cell models: A tool for filling the gaps in knowledge for human genetic diseasesIvana Antonucci, Marci G Crowley, Liborio Stuppia
International Journal of Molecular Sciences|April 11, 2012
Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseasesLiborio Stuppia, Ivana Antonucci, Giandomenico Palka, et al.
Fertility and Sterility|February 17, 2017
Male factor infertility and lack of openness about infertility as risk factors for depressive symptoms in males undergoing assisted reproductive technology treatment in ItalyAlessandra Babore, Liborio Stuppia, Carmen Trumello, et al.
Biomedicines|January 8, 2025
Microbiota and Autism: A Review on Oral and Gut Microbiome Analysis Through 16S rRNA SequencingFederico Anaclerio, Maria Minelli, Ivana Antonucci, et al.
Clinical Epigenetics|November 14, 2015
Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime healthLiborio Stuppia, Marica Franzago, Patrizia Ballerini, et al.
Haematologica|January 19, 2007
Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cellsAlessia Colosimo, Valentina Guida, Ivana Antonucci, et al.
Asian Journal of Andrology|July 27, 2010
Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocolsRossella Giuliani, Ivana Antonucci, Isabella Torrente, et al.
Clinical Case Reports|March 8, 2017
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancerIvana Antonucci, Martina Provenzano, Luca Sorino, et al.
Pageof 8