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Monica Miozzo

Showing results (81-90 of 100) with videos related to

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Clinical Genetics|November 25, 2018
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twinsLeda Paganini, Loubna A Hadi, Massimiliano Chetta, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 24, 2005
X chromosome monosomy: a common mechanism for autoimmune diseasesPietro Invernizzi, Monica Miozzo, Carlo Selmi, et al.
Stem Cells and Development|May 25, 2016
The Adipose Mesenchymal Stem Cell Secretome Inhibits Inflammatory Responses of Microglia: Evidence for an Involvement of Sphingosine-1-Phosphate SignallingGiovanni Marfia, Stefania Elena Navone, Loubna Abdel Hadi, et al.
International Journal of Molecular Sciences|May 28, 2022
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. <i>Int. J. Mol. Sci.</i> 2021, <i>22</i>, 2136Ornella Rondinone, Alessio Murgia, Jole Costanza, et al.
International Journal of Molecular Sciences|March 6, 2021
Extensive Placental Methylation Profiling in Normal PregnanciesOrnella Rondinone, Alessio Murgia, Jole Costanza, et al.
Thyroid : Official Journal of the American Thyroid Association|December 4, 2018
Impact of Mutation Density and Heterogeneity on Papillary Thyroid Cancer Clinical Features and Remission ProbabilityCarla Colombo, Marina Muzza, Maria Carla Proverbio, et al.
Leukemia Research|December 16, 2014
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosisClaudia Augello, Umberto Gianelli, Rossella Falcone, et al.
Annals of the New York Academy of Sciences|October 4, 2007
X monosomy in female systemic lupus erythematosusPietro Invernizzi, Monica Miozzo, Sabine Oertelt-Prigione, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 13, 2021
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic BrachydactylyFrancesca Marta Elli, Deborah Mattinzoli, Camilla Lucca, et al.
European Journal of Cancer (Oxford, England : 1990)|June 17, 2022
Copy number alterations in stage I epithelial ovarian cancer highlight three genomic patterns associated with prognosisChiara Pesenti, Luca Beltrame, Angelo Velle, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
Clinical Genetics|November 25, 2018
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twinsLeda Paganini, Loubna A Hadi, Massimiliano Chetta, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 24, 2005
X chromosome monosomy: a common mechanism for autoimmune diseasesPietro Invernizzi, Monica Miozzo, Carlo Selmi, et al.
Stem Cells and Development|May 25, 2016
The Adipose Mesenchymal Stem Cell Secretome Inhibits Inflammatory Responses of Microglia: Evidence for an Involvement of Sphingosine-1-Phosphate SignallingGiovanni Marfia, Stefania Elena Navone, Loubna Abdel Hadi, et al.
International Journal of Molecular Sciences|May 28, 2022
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. <i>Int. J. Mol. Sci.</i> 2021, <i>22</i>, 2136Ornella Rondinone, Alessio Murgia, Jole Costanza, et al.
International Journal of Molecular Sciences|March 6, 2021
Extensive Placental Methylation Profiling in Normal PregnanciesOrnella Rondinone, Alessio Murgia, Jole Costanza, et al.
Thyroid : Official Journal of the American Thyroid Association|December 4, 2018
Impact of Mutation Density and Heterogeneity on Papillary Thyroid Cancer Clinical Features and Remission ProbabilityCarla Colombo, Marina Muzza, Maria Carla Proverbio, et al.
Leukemia Research|December 16, 2014
PDGFB hypomethylation is a favourable prognostic biomarker in primary myelofibrosisClaudia Augello, Umberto Gianelli, Rossella Falcone, et al.
Annals of the New York Academy of Sciences|October 4, 2007
X monosomy in female systemic lupus erythematosusPietro Invernizzi, Monica Miozzo, Sabine Oertelt-Prigione, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 13, 2021
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic BrachydactylyFrancesca Marta Elli, Deborah Mattinzoli, Camilla Lucca, et al.
European Journal of Cancer (Oxford, England : 1990)|June 17, 2022
Copy number alterations in stage I epithelial ovarian cancer highlight three genomic patterns associated with prognosisChiara Pesenti, Luca Beltrame, Angelo Velle, et al.
Pageof 10