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Monica Miozzo

Showing results (51-60 of 100) with videos related to

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Current Pharmaceutical Biotechnology|May 20, 2016
H2020 and Beyond: Skip Discrepancy between Theory and Practice of Personalized Medicine. A Position Paper by the Italian Society of Personalized MedicineMarina Borro, Maurizio Simmaco, Antonio Aceti, et al.
Human Reproduction (Oxford, England)|October 16, 2014
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic menAlessandra Pansa, Silvia M Sirchia, Sara Melis, et al.
European Journal of Human Genetics : EJHG|January 19, 2006
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villiFrancesca R Grati, Beatrice Grimi, Giuditia Frascoli, et al.
Journal of Autoimmunity|February 5, 2013
Y chromosome loss in male patients with primary biliary cirrhosisAna Lleo, Sabine Oertelt-Prigione, Ilaria Bianchi, et al.
Oncotarget|September 17, 2017
Mass spectrometry-based assay for the molecular diagnosis of glioma: concomitant detection of chromosome 1p/19q codeletion, and <i>IDH1</i>, <i>IDH2</i>, and <i>TERT</i> mutation statusChiara Pesenti, Leda Paganini, Laura Fontana, et al.
Plos One|March 8, 2013
Delineating the cytogenomic and epigenomic landscapes of glioma stem cell linesSimona Baronchelli, Angela Bentivegna, Serena Redaelli, et al.
Orphanet Journal of Rare Diseases|November 6, 2009
Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reportsLaura Bernardini, Stefania Gimelli, Cristina Gervasini, et al.
American Journal of Medical Genetics. Part A|June 16, 2005
Three cases with de novo 6q imbalance and variable prenatal phenotypeFrancesca R Grati, Faustina Lalatta, Licia Turolla, et al.
Biomolecules|November 27, 2021
Cohesin Mutations Induce Chromatin Conformation Perturbation of the <i>H19</i>/<i>IGF2</i> Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange Syndrome Cell LinesSilvana Pileggi, Marta La Vecchia, Elisa Adele Colombo, et al.
Diagnostic Pathology|January 26, 2018
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometryEleonora Bonaparte, Chiara Pesenti, Laura Fontana, et al.
Pageof 10

Showing results (51-60 of 100) with videos related to

Sort By:
Pageof 10
Current Pharmaceutical Biotechnology|May 20, 2016
H2020 and Beyond: Skip Discrepancy between Theory and Practice of Personalized Medicine. A Position Paper by the Italian Society of Personalized MedicineMarina Borro, Maurizio Simmaco, Antonio Aceti, et al.
Human Reproduction (Oxford, England)|October 16, 2014
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic menAlessandra Pansa, Silvia M Sirchia, Sara Melis, et al.
European Journal of Human Genetics : EJHG|January 19, 2006
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villiFrancesca R Grati, Beatrice Grimi, Giuditia Frascoli, et al.
Journal of Autoimmunity|February 5, 2013
Y chromosome loss in male patients with primary biliary cirrhosisAna Lleo, Sabine Oertelt-Prigione, Ilaria Bianchi, et al.
Oncotarget|September 17, 2017
Mass spectrometry-based assay for the molecular diagnosis of glioma: concomitant detection of chromosome 1p/19q codeletion, and <i>IDH1</i>, <i>IDH2</i>, and <i>TERT</i> mutation statusChiara Pesenti, Leda Paganini, Laura Fontana, et al.
Plos One|March 8, 2013
Delineating the cytogenomic and epigenomic landscapes of glioma stem cell linesSimona Baronchelli, Angela Bentivegna, Serena Redaelli, et al.
Orphanet Journal of Rare Diseases|November 6, 2009
Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reportsLaura Bernardini, Stefania Gimelli, Cristina Gervasini, et al.
American Journal of Medical Genetics. Part A|June 16, 2005
Three cases with de novo 6q imbalance and variable prenatal phenotypeFrancesca R Grati, Faustina Lalatta, Licia Turolla, et al.
Biomolecules|November 27, 2021
Cohesin Mutations Induce Chromatin Conformation Perturbation of the <i>H19</i>/<i>IGF2</i> Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange Syndrome Cell LinesSilvana Pileggi, Marta La Vecchia, Elisa Adele Colombo, et al.
Diagnostic Pathology|January 26, 2018
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometryEleonora Bonaparte, Chiara Pesenti, Laura Fontana, et al.
Pageof 10