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Joussef Hayek

Showing results (71-80 of 85) with videos related to

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Biopolymers|May 15, 2015
Antibody recognition in multiple sclerosis and Rett syndrome using a collection of linear and cyclic N-glucosylated antigenic probesFeliciana Real Fernández, Margherita Di Pisa, Giada Rossi, et al.
Molecular and Cellular Biochemistry|January 8, 2017
Oxygen exchange and energy metabolism in erythrocytes of Rett syndrome and their relationships with respiratory alterationsChiara Ciaccio, Donato Di Pierro, Diego Sbardella, et al.
Journal of Immunology Research|November 13, 2014
Immune dysfunction in Rett syndrome patients revealed by high levels of serum anti-N(Glc) IgM antibody fractionAnna Maria Papini, Francesca Nuti, Feliciana Real-Fernandez, et al.
Scientific Reports|September 28, 2017
Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett SyndromeDiego Sbardella, Grazia Raffaella Tundo, Luisa Campagnolo, et al.
Biomolecules|May 28, 2025
<i>MECP2</i> mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA MappingMartina Mietto, Silvia Montanari, Maria Sofia Falzarano, et al.
Oxidative Medicine and Cellular Longevity|July 3, 2014
Redox imbalance and morphological changes in skin fibroblasts in typical Rett syndromeCinzia Signorini, Silvia Leoncini, Claudio De Felice, et al.
Plos One|March 8, 2013
Revealing the complexity of a monogenic disease: rett syndrome exome sequencingElisa Grillo, Caterina Lo Rizzo, Laura Bianciardi, et al.
Neuroscience Research|October 18, 2015
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndromeAlessio Cortelazzo, Claudio De Felice, Roberto Guerranti, et al.
Neurobiology of Disease|April 29, 2014
Oxidative brain damage in Mecp2-mutant murine models of Rett syndromeClaudio De Felice, Floriana Della Ragione, Cinzia Signorini, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 11, 2020
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutationsDiego Sbardella, Grazia Raffaella Tundo, Vincenzo Cunsolo, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Biopolymers|May 15, 2015
Antibody recognition in multiple sclerosis and Rett syndrome using a collection of linear and cyclic N-glucosylated antigenic probesFeliciana Real Fernández, Margherita Di Pisa, Giada Rossi, et al.
Molecular and Cellular Biochemistry|January 8, 2017
Oxygen exchange and energy metabolism in erythrocytes of Rett syndrome and their relationships with respiratory alterationsChiara Ciaccio, Donato Di Pierro, Diego Sbardella, et al.
Journal of Immunology Research|November 13, 2014
Immune dysfunction in Rett syndrome patients revealed by high levels of serum anti-N(Glc) IgM antibody fractionAnna Maria Papini, Francesca Nuti, Feliciana Real-Fernandez, et al.
Scientific Reports|September 28, 2017
Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett SyndromeDiego Sbardella, Grazia Raffaella Tundo, Luisa Campagnolo, et al.
Biomolecules|May 28, 2025
<i>MECP2</i> mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA MappingMartina Mietto, Silvia Montanari, Maria Sofia Falzarano, et al.
Oxidative Medicine and Cellular Longevity|July 3, 2014
Redox imbalance and morphological changes in skin fibroblasts in typical Rett syndromeCinzia Signorini, Silvia Leoncini, Claudio De Felice, et al.
Plos One|March 8, 2013
Revealing the complexity of a monogenic disease: rett syndrome exome sequencingElisa Grillo, Caterina Lo Rizzo, Laura Bianciardi, et al.
Neuroscience Research|October 18, 2015
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndromeAlessio Cortelazzo, Claudio De Felice, Roberto Guerranti, et al.
Neurobiology of Disease|April 29, 2014
Oxidative brain damage in Mecp2-mutant murine models of Rett syndromeClaudio De Felice, Floriana Della Ragione, Cinzia Signorini, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 11, 2020
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutationsDiego Sbardella, Grazia Raffaella Tundo, Vincenzo Cunsolo, et al.
Pageof 9