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Maurizio Ferrari

Showing results (51-60 of 186) with videos related to

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Plos One|December 19, 2018
Analysis of KRAS, NRAS and BRAF mutational profile by combination of in-tube hybridization and universal tag-microarray in tumor tissue and plasma of colorectal cancer patientsFrancesco Damin, Silvia Galbiati, Nadia Soriani, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Skewed X-chromosome inactivation is not associated with premature ovarian failure in a large cohort of Italian patientsSilvia Bione, Sara Benedetti, Mara Goegan, et al.
Archivos De Bronconeumologia|February 7, 2012
A child with severe pneumomediastinum and ABCA3 gene mutation: a puzzling connectionMarco Copertino, Egidio Barbi, Furio Poli, et al.
Clinical Chemistry and Laboratory Medicine|April 8, 2014
Further considerations concerning non-invasive prenatal diagnosis of craniosynostosis based on the identification of an 18 bp deletion in the TWIST1 gene by COLD-PCRSilvia Galbiati, Stefania Stenirri, Luca Sbaiz, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 11, 2014
Evaluation of damaging effects of splicing mutations: validation of an in vitro method for diagnostic laboratoriesChiara Di Resta, Martina Manzoni, Massimo Zoni Berisso, et al.
Clinical Chemistry|October 27, 2010
Full COLD-PCR protocol for noninvasive prenatal diagnosis of genetic diseasesSilvia Galbiati, Angela Brisci, Faustina Lalatta, et al.
Materials (Basel, Switzerland)|October 17, 2019
Synthesis and Post-Annealing of Cu<sub>2</sub>ZnSnS<sub>4</sub> Absorber Layers Based on Oleylamine/1-dodecanethiolNarges Ataollahi, Francesca Bazerla, Claudia Malerba, et al.
Human Reproduction (Oxford, England)|May 24, 2019
ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuriaArvand Akbari, Giovanni Battista Pipitone, Zahra Anvar, et al.
Clinical Chemistry and Laboratory Medicine|June 14, 2023
Toolkit for emerging technologies in laboratory medicineRonda Greaves, Larry Kricka, Damien Gruson, et al.
Journal of Neurology|December 17, 2014
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutationMarina Scarlato, Arturo Nuara, Simonetta Gerevini, et al.
Pageof 19

Showing results (51-60 of 186) with videos related to

Sort By:
Pageof 19
Plos One|December 19, 2018
Analysis of KRAS, NRAS and BRAF mutational profile by combination of in-tube hybridization and universal tag-microarray in tumor tissue and plasma of colorectal cancer patientsFrancesco Damin, Silvia Galbiati, Nadia Soriani, et al.
American Journal of Medical Genetics. Part A|May 13, 2006
Skewed X-chromosome inactivation is not associated with premature ovarian failure in a large cohort of Italian patientsSilvia Bione, Sara Benedetti, Mara Goegan, et al.
Archivos De Bronconeumologia|February 7, 2012
A child with severe pneumomediastinum and ABCA3 gene mutation: a puzzling connectionMarco Copertino, Egidio Barbi, Furio Poli, et al.
Clinical Chemistry and Laboratory Medicine|April 8, 2014
Further considerations concerning non-invasive prenatal diagnosis of craniosynostosis based on the identification of an 18 bp deletion in the TWIST1 gene by COLD-PCRSilvia Galbiati, Stefania Stenirri, Luca Sbaiz, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 11, 2014
Evaluation of damaging effects of splicing mutations: validation of an in vitro method for diagnostic laboratoriesChiara Di Resta, Martina Manzoni, Massimo Zoni Berisso, et al.
Clinical Chemistry|October 27, 2010
Full COLD-PCR protocol for noninvasive prenatal diagnosis of genetic diseasesSilvia Galbiati, Angela Brisci, Faustina Lalatta, et al.
Materials (Basel, Switzerland)|October 17, 2019
Synthesis and Post-Annealing of Cu<sub>2</sub>ZnSnS<sub>4</sub> Absorber Layers Based on Oleylamine/1-dodecanethiolNarges Ataollahi, Francesca Bazerla, Claudia Malerba, et al.
Human Reproduction (Oxford, England)|May 24, 2019
ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuriaArvand Akbari, Giovanni Battista Pipitone, Zahra Anvar, et al.
Clinical Chemistry and Laboratory Medicine|June 14, 2023
Toolkit for emerging technologies in laboratory medicineRonda Greaves, Larry Kricka, Damien Gruson, et al.
Journal of Neurology|December 17, 2014
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutationMarina Scarlato, Arturo Nuara, Simonetta Gerevini, et al.
Pageof 19