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Daniela De Rocco

Showing results (1-10 of 37) with videos related to

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Platelets|April 4, 2017
MYH9 gene mutations associated with bleedingAnna Savoia, Daniela De Rocco, Alessandro Pecci
International Journal of Molecular Sciences|October 13, 2021
A Novel Mutation in <i>GP1BB</i> Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex AssemblySerena Barozzi, Valeria Bozzi, Daniela De Rocco, et al.
Platelets|January 28, 2009
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown originAnna Savoia, Patrizia Noris, Silverio Perrotta, et al.
European Journal of Medical Genetics|May 20, 2009
Identification of the first duplication in MYH9-related disease: a hot spot for unequal crossing-over within exon 24 of the MYH9 geneDaniela De Rocco, Nuria Pujol-Moix, Alessandro Pecci, et al.
Biochimica Et Biophysica Acta|April 8, 2014
Unusual splice site mutations disrupt FANCA exon 8 definitionChiara Mattioli, Giulia Pianigiani, Daniela De Rocco, et al.
Microorganisms|October 1, 2020
Renin Angiotensin System, COVID-19 and Male Fertility: Any Risk for Conceiving?Lorella Pascolo, Gabriella Zito, Luisa Zupin, et al.
Cytokine|March 15, 2015
Impaired immune response to Candida albicans in cells from Fanconi anemia patientsAlessia Parodi, Francesca Kalli, Johanna Svahn, et al.
European Journal of Medical Genetics|July 7, 2010
A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defectSilvia Vettore, Daniela De Rocco, Bernhard Gerber, et al.
British Journal of Haematology|May 4, 2017
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin genePatrizia Noris, Caterina Marconi, Daniela De Rocco, et al.
Hamostaseologie|July 12, 2018
MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the DisorderCarlo Zaninetti, Daniela De Rocco, Tania Giangregorio, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Platelets|April 4, 2017
MYH9 gene mutations associated with bleedingAnna Savoia, Daniela De Rocco, Alessandro Pecci
International Journal of Molecular Sciences|October 13, 2021
A Novel Mutation in <i>GP1BB</i> Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex AssemblySerena Barozzi, Valeria Bozzi, Daniela De Rocco, et al.
Platelets|January 28, 2009
Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown originAnna Savoia, Patrizia Noris, Silverio Perrotta, et al.
European Journal of Medical Genetics|May 20, 2009
Identification of the first duplication in MYH9-related disease: a hot spot for unequal crossing-over within exon 24 of the MYH9 geneDaniela De Rocco, Nuria Pujol-Moix, Alessandro Pecci, et al.
Biochimica Et Biophysica Acta|April 8, 2014
Unusual splice site mutations disrupt FANCA exon 8 definitionChiara Mattioli, Giulia Pianigiani, Daniela De Rocco, et al.
Microorganisms|October 1, 2020
Renin Angiotensin System, COVID-19 and Male Fertility: Any Risk for Conceiving?Lorella Pascolo, Gabriella Zito, Luisa Zupin, et al.
Cytokine|March 15, 2015
Impaired immune response to Candida albicans in cells from Fanconi anemia patientsAlessia Parodi, Francesca Kalli, Johanna Svahn, et al.
European Journal of Medical Genetics|July 7, 2010
A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defectSilvia Vettore, Daniela De Rocco, Bernhard Gerber, et al.
British Journal of Haematology|May 4, 2017
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin genePatrizia Noris, Caterina Marconi, Daniela De Rocco, et al.
Hamostaseologie|July 12, 2018
MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the DisorderCarlo Zaninetti, Daniela De Rocco, Tania Giangregorio, et al.
Pageof 4