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P Chiurazzi

Showing results (31-40 of 49) with videos related to

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American Journal of Medical Genetics|July 15, 1994
No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndromeP Chiurazzi, E de Graaff, J Ng, et al.
Human Molecular Genetics|February 28, 2006
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modificationsM L De Bonis, A Cerase, M R Matarazzo, et al.
Journal of Medical Genetics|June 17, 2003
Modulation of methylation in the FMR1 promoter region after long term treatment with L-carnitine and acetyl-L-carnitineE Pascale, E Battiloro, G Cimino Reale, et al.
European Review for Medical and Pharmacological Sciences|July 13, 2019
Genetics of lipedema: new perspectives on genetic research and molecular diagnosesS Paolacci, V Precone, F Acquaviva, et al.
La Clinica Terapeutica|November 23, 2023
Reduction of nitrosamines in cigarette smoke vapors through a filter functionalized with polyphenols from olive treeK Donato, A Macchia, G Bonetti, et al.
American Journal of Medical Genetics|July 12, 1996
Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneityP Chiurazzi, M Genuardi, L Kozak, et al.
European Review for Medical and Pharmacological Sciences|December 19, 2023
Metabolomic profiling of amino acid alterations in anorexia nervosa: implications for appetite regulation and therapeutic strategiesK Donato, K Dhuli, A Macchia, et al.
European Review for Medical and Pharmacological Sciences|May 20, 2024
Retraction Note: Metabolomic profiling of amino acid alterations in anorexia nervosa: implications for appetite regulation and therapeutic strategiesK Donato, K Dhuli, A Macchia, et al.
European Review for Medical and Pharmacological Sciences|December 19, 2023
AKR1C1 and hormone metabolism in lipedema pathogenesis: a computational biology approachJ Kaftalli, G Bonetti, G Marceddu, et al.
American Journal of Medical Genetics|July 9, 1999
Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patientsM Grasso, F Faravelli, C Lo Nigro, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|July 15, 1994
No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndromeP Chiurazzi, E de Graaff, J Ng, et al.
Human Molecular Genetics|February 28, 2006
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modificationsM L De Bonis, A Cerase, M R Matarazzo, et al.
Journal of Medical Genetics|June 17, 2003
Modulation of methylation in the FMR1 promoter region after long term treatment with L-carnitine and acetyl-L-carnitineE Pascale, E Battiloro, G Cimino Reale, et al.
European Review for Medical and Pharmacological Sciences|July 13, 2019
Genetics of lipedema: new perspectives on genetic research and molecular diagnosesS Paolacci, V Precone, F Acquaviva, et al.
La Clinica Terapeutica|November 23, 2023
Reduction of nitrosamines in cigarette smoke vapors through a filter functionalized with polyphenols from olive treeK Donato, A Macchia, G Bonetti, et al.
American Journal of Medical Genetics|July 12, 1996
Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneityP Chiurazzi, M Genuardi, L Kozak, et al.
European Review for Medical and Pharmacological Sciences|December 19, 2023
Metabolomic profiling of amino acid alterations in anorexia nervosa: implications for appetite regulation and therapeutic strategiesK Donato, K Dhuli, A Macchia, et al.
European Review for Medical and Pharmacological Sciences|May 20, 2024
Retraction Note: Metabolomic profiling of amino acid alterations in anorexia nervosa: implications for appetite regulation and therapeutic strategiesK Donato, K Dhuli, A Macchia, et al.
European Review for Medical and Pharmacological Sciences|December 19, 2023
AKR1C1 and hormone metabolism in lipedema pathogenesis: a computational biology approachJ Kaftalli, G Bonetti, G Marceddu, et al.
American Journal of Medical Genetics|July 9, 1999
Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patientsM Grasso, F Faravelli, C Lo Nigro, et al.
Pageof 5