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Giovanni Neri

Showing results (121-130 of 273) with videos related to

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American Journal of Medical Genetics. Part A|March 16, 2012
Expanding the spectrum of rearrangements involving chromosome 19: a mild phenotype associated with a 19p13.12-p13.13 deletionGiuseppe Marangi, Daniela Orteschi, Federico Vigevano, et al.
International Journal of Molecular Sciences|August 14, 2025
Supramolecular Graphene Quantum Dots/Porphyrin Complex as Fluorescence Probe for Metal Ion SensingMariachiara Sarà, Andrea Romeo, Gabriele Lando, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 18, 2012
Photoreduction of mesoporous In2O3: mechanistic model and utility in gas sensingThorsten Wagner, Claus-Dieter Kohl, Sara Morandi, et al.
Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 1, 2008
Correlation between GJB2 mutations and audiological deficits: personal experiencePasqualina M Picciotti, Roberta Pietrobono, Giovanni Neri, et al.
Journal of Environmental Sciences (China)|November 3, 2023
A novel 2D-GO@WS2 electrochemical platform for the determination of thiram fungicideKhouloud Abid, Daniela Iannazzo, Consuelo Celesti, et al.
Epigenetics & Chromatin|March 26, 2016
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cellsElisabetta Tabolacci, Giorgia Mancano, Stella Lanni, et al.
Autism Research : Official Journal of the International Society for Autism Research|August 15, 2009
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorderPamela B Jackson, Luigi Boccuto, Cindy Skinner, et al.
ACS Omega|April 27, 2026
Graphene Dot-ZnO Hybrid Nanostructures as High-Performance Chemiresistive Sensors for H<sub>2</sub>S DetectionFederica Bucolo, Daniela Iannazzo, Nesrine Hafiene, et al.
Marine Environmental Research|June 5, 2004
Evaluation of ecotoxicological effects of endocrine disrupters during a four-year survey of the Mediterranean population of swordfish (Xiphias gladius)M Cristina Fossi, Silvia Casini, Letizia Marsili, et al.
Pageof 28

Showing results (121-130 of 273) with videos related to

Sort By:
Pageof 28
American Journal of Medical Genetics. Part A|March 16, 2012
Expanding the spectrum of rearrangements involving chromosome 19: a mild phenotype associated with a 19p13.12-p13.13 deletionGiuseppe Marangi, Daniela Orteschi, Federico Vigevano, et al.
International Journal of Molecular Sciences|August 14, 2025
Supramolecular Graphene Quantum Dots/Porphyrin Complex as Fluorescence Probe for Metal Ion SensingMariachiara Sarà, Andrea Romeo, Gabriele Lando, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|May 18, 2012
Photoreduction of mesoporous In2O3: mechanistic model and utility in gas sensingThorsten Wagner, Claus-Dieter Kohl, Sara Morandi, et al.
Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 1, 2008
Correlation between GJB2 mutations and audiological deficits: personal experiencePasqualina M Picciotti, Roberta Pietrobono, Giovanni Neri, et al.
Journal of Environmental Sciences (China)|November 3, 2023
A novel 2D-GO@WS2 electrochemical platform for the determination of thiram fungicideKhouloud Abid, Daniela Iannazzo, Consuelo Celesti, et al.
Epigenetics & Chromatin|March 26, 2016
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cellsElisabetta Tabolacci, Giorgia Mancano, Stella Lanni, et al.
Autism Research : Official Journal of the International Society for Autism Research|August 15, 2009
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorderPamela B Jackson, Luigi Boccuto, Cindy Skinner, et al.
ACS Omega|April 27, 2026
Graphene Dot-ZnO Hybrid Nanostructures as High-Performance Chemiresistive Sensors for H<sub>2</sub>S DetectionFederica Bucolo, Daniela Iannazzo, Nesrine Hafiene, et al.
Marine Environmental Research|June 5, 2004
Evaluation of ecotoxicological effects of endocrine disrupters during a four-year survey of the Mediterranean population of swordfish (Xiphias gladius)M Cristina Fossi, Silvia Casini, Letizia Marsili, et al.
Pageof 28