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Emilia Vitale

Showing results (1-10 of 21) with videos related to

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The Neurologist|September 11, 2009
Structural chromosomal variations in neurological diseasesBernadette Kalman, Emilia Vitale
Non-Coding RNA|November 17, 2020
LINC00473 as an Immediate Early Gene under the Control of the EGR1 Transcription FactorVincenza Aliperti, Emilia Vitale, Francesco Aniello, et al.
International Journal of Molecular Sciences|March 31, 2019
Identification, Characterization, and Regulatory Mechanisms of a Novel EGR1 Splicing IsoformVincenza Aliperti, Giulia Sgueglia, Francesco Aniello, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitusCagri Yildirim-Toruner, Kavitha Subramanian, Lamya El Manjra, et al.
Molecular Neurobiology|June 28, 2024
Sustained Depolarization Induces Gene Expression Pattern Changes Related to Synaptic Plasticity in a Human Cholinergic Cellular ModelAnna Maria Carrese, Rossella Vitale, Manuela Turco, et al.
International Journal of Molecular Sciences|April 12, 2022
CD33 rs2455069 SNP: Correlation with Alzheimer's Disease and Hypothesis of Functional RoleFabiana Tortora, Antonella Rendina, Antonella Angiolillo, et al.
Journal of Biochemical and Molecular Toxicology|October 6, 2025
Bisphenol A Treatment Impairs Synaptic Function in Human Cholinergic NeuronsAnna Maria Carrese, Rossella Vitale, Manuela Turco, et al.
Plos One|July 10, 2008
Variants of ST8SIA1 are associated with risk of developing multiple sclerosisSeema Husain, Cagri Yildirim-Toruner, Justin P Rubio, et al.
Human Molecular Genetics|February 2, 2002
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12Emilia Vitale, Stuart Cook, Rong Sun, et al.
American Journal of Medical Genetics. Part A|June 6, 2014
Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disabilityEric R Londin, Jeffrey Adijanto, Nancy Philp, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
The Neurologist|September 11, 2009
Structural chromosomal variations in neurological diseasesBernadette Kalman, Emilia Vitale
Non-Coding RNA|November 17, 2020
LINC00473 as an Immediate Early Gene under the Control of the EGR1 Transcription FactorVincenza Aliperti, Emilia Vitale, Francesco Aniello, et al.
International Journal of Molecular Sciences|March 31, 2019
Identification, Characterization, and Regulatory Mechanisms of a Novel EGR1 Splicing IsoformVincenza Aliperti, Giulia Sgueglia, Francesco Aniello, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitusCagri Yildirim-Toruner, Kavitha Subramanian, Lamya El Manjra, et al.
Molecular Neurobiology|June 28, 2024
Sustained Depolarization Induces Gene Expression Pattern Changes Related to Synaptic Plasticity in a Human Cholinergic Cellular ModelAnna Maria Carrese, Rossella Vitale, Manuela Turco, et al.
International Journal of Molecular Sciences|April 12, 2022
CD33 rs2455069 SNP: Correlation with Alzheimer's Disease and Hypothesis of Functional RoleFabiana Tortora, Antonella Rendina, Antonella Angiolillo, et al.
Journal of Biochemical and Molecular Toxicology|October 6, 2025
Bisphenol A Treatment Impairs Synaptic Function in Human Cholinergic NeuronsAnna Maria Carrese, Rossella Vitale, Manuela Turco, et al.
Plos One|July 10, 2008
Variants of ST8SIA1 are associated with risk of developing multiple sclerosisSeema Husain, Cagri Yildirim-Toruner, Justin P Rubio, et al.
Human Molecular Genetics|February 2, 2002
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12Emilia Vitale, Stuart Cook, Rong Sun, et al.
American Journal of Medical Genetics. Part A|June 6, 2014
Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disabilityEric R Londin, Jeffrey Adijanto, Nancy Philp, et al.
Pageof 3