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Rita Cacace

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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 27, 2016
Molecular genetics of early-onset Alzheimer's disease revisitedRita Cacace, Kristel Sleegers, Christine Van Broeckhoven
Alzheimer'S & Dementia (Amsterdam, Netherlands)|March 5, 2021
Insight into the genetic etiology of Alzheimer's disease: A comprehensive review of the role of rare variantsJulie Hoogmartens, Rita Cacace, Christine Van Broeckhoven
Molecular Neurodegeneration|April 28, 2022
The role of ATP-binding cassette subfamily A in the etiology of Alzheimer's diseaseLiene Bossaerts, Rita Cacace, Christine Van Broeckhoven
Genome Medicine|April 15, 2021
Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseasesFederica Perrone, Rita Cacace, Julie van der Zee, et al.
Neurobiology of Aging|October 8, 2021
Genetic variants in progranulin upstream open reading frames increase downstream protein expressionAlexandros Frydas, Rita Cacace, Julie van der Zee, et al.
Frontiers in Genetics|March 13, 2025
Investigation of the role of miRNA variants in neurodegenerative brain diseasesAlexandros Frydas, Rita Cacace, Julie van der Zee, et al.
Acta Neuropathologica Communications|April 1, 2022
Rare missense mutations in ABCA7 might increase Alzheimer's disease risk by plasma membrane exclusionLiene Bossaerts, Elisabeth Hendrickx Van de Craen, Rita Cacace, et al.
Neurobiology of Aging|October 7, 2020
Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's diseaseJulie Hoogmartens, Elisabeth Hens, Sebastiaan Engelborghs, et al.
Neurobiology of Aging|April 24, 2021
Investigation of the role of matrix metalloproteinases in the genetic etiology of Alzheimer's diseaseJulie Hoogmartens, Elisabeth Hens, Sebastiaan Engelborghs, et al.
Neurobiology of Aging|June 4, 2018
Genetic screening in early-onset dementia patients with unclear phenotype: relevance for clinical diagnosisFederica Perrone, Rita Cacace, Sara Van Mossevelde, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 27, 2016
Molecular genetics of early-onset Alzheimer's disease revisitedRita Cacace, Kristel Sleegers, Christine Van Broeckhoven
Alzheimer'S & Dementia (Amsterdam, Netherlands)|March 5, 2021
Insight into the genetic etiology of Alzheimer's disease: A comprehensive review of the role of rare variantsJulie Hoogmartens, Rita Cacace, Christine Van Broeckhoven
Molecular Neurodegeneration|April 28, 2022
The role of ATP-binding cassette subfamily A in the etiology of Alzheimer's diseaseLiene Bossaerts, Rita Cacace, Christine Van Broeckhoven
Genome Medicine|April 15, 2021
Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseasesFederica Perrone, Rita Cacace, Julie van der Zee, et al.
Neurobiology of Aging|October 8, 2021
Genetic variants in progranulin upstream open reading frames increase downstream protein expressionAlexandros Frydas, Rita Cacace, Julie van der Zee, et al.
Frontiers in Genetics|March 13, 2025
Investigation of the role of miRNA variants in neurodegenerative brain diseasesAlexandros Frydas, Rita Cacace, Julie van der Zee, et al.
Acta Neuropathologica Communications|April 1, 2022
Rare missense mutations in ABCA7 might increase Alzheimer's disease risk by plasma membrane exclusionLiene Bossaerts, Elisabeth Hendrickx Van de Craen, Rita Cacace, et al.
Neurobiology of Aging|October 7, 2020
Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's diseaseJulie Hoogmartens, Elisabeth Hens, Sebastiaan Engelborghs, et al.
Neurobiology of Aging|April 24, 2021
Investigation of the role of matrix metalloproteinases in the genetic etiology of Alzheimer's diseaseJulie Hoogmartens, Elisabeth Hens, Sebastiaan Engelborghs, et al.
Neurobiology of Aging|June 4, 2018
Genetic screening in early-onset dementia patients with unclear phenotype: relevance for clinical diagnosisFederica Perrone, Rita Cacace, Sara Van Mossevelde, et al.
Pageof 2