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Donatella Nocera

Showing results (1-10 of 5) with videos related to

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Genes & Development|October 17, 2003
The spindle checkpoint requires cyclin-dependent kinase activityVincenzo D'Angiolella, Cecilia Mari, Donatella Nocera, et al.
Case Reports in Genetics|March 20, 2013
A case of premature ovarian failure in a 33-year-old womanEmma Colao, Teresa Granata, Marco F M Vismara, et al.
Genes|January 23, 2024
Non-Invasive Prenatal Test Analysis Opens a Pandora's Box: Identification of Very Rare Cases of SRY-Positive Healthy Females, Segregating for Three Generations Thanks to Preferential Inactivation of the XqYp Translocated ChromosomeCristina Politi, Katia Grillone, Donatella Nocera, et al.
Dermatology Online Journal|January 29, 2011
Identification of a new mutation in the gene coding for hairless protein responsible for alopecia universalis: The importance of direct gene sequencingStefania Nucara, Emma Colao, Graziella Mangone, et al.
Acta Diabetologica|April 10, 2019
Functional characterization of p.Pro409His variant in HNF1A, a hypomorphic mutation involved in pancreatic β-cell dysfunctionDonatella Nocera, Miranda Menniti, Stefania Belviso, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Genes & Development|October 17, 2003
The spindle checkpoint requires cyclin-dependent kinase activityVincenzo D'Angiolella, Cecilia Mari, Donatella Nocera, et al.
Case Reports in Genetics|March 20, 2013
A case of premature ovarian failure in a 33-year-old womanEmma Colao, Teresa Granata, Marco F M Vismara, et al.
Genes|January 23, 2024
Non-Invasive Prenatal Test Analysis Opens a Pandora's Box: Identification of Very Rare Cases of SRY-Positive Healthy Females, Segregating for Three Generations Thanks to Preferential Inactivation of the XqYp Translocated ChromosomeCristina Politi, Katia Grillone, Donatella Nocera, et al.
Dermatology Online Journal|January 29, 2011
Identification of a new mutation in the gene coding for hairless protein responsible for alopecia universalis: The importance of direct gene sequencingStefania Nucara, Emma Colao, Graziella Mangone, et al.
Acta Diabetologica|April 10, 2019
Functional characterization of p.Pro409His variant in HNF1A, a hypomorphic mutation involved in pancreatic β-cell dysfunctionDonatella Nocera, Miranda Menniti, Stefania Belviso, et al.
Pageof 1