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Showing results (161-170 of 167) with videos related to

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The Journal of Clinical Investigation|February 1, 2022
Targeting the ASMase/S1P pathway protects from sortilin-evoked vascular damage in hypertensionPaola Di Pietro, Albino Carrizzo, Eduardo Sommella, et al.
BMC Medical Genetics|January 25, 2013
Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetesNatalia V Rivera, Robert Carreras-Torres, Roberta Roncarati, et al.
Neurobiology of Aging|July 9, 2015
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaRaffaele Ferrari, Mario Grassi, Erika Salvi, et al.
Genome Research|May 27, 2011
A DNA methylation fingerprint of 1628 human samplesAgustin F Fernandez, Yassen Assenov, Jose Ignacio Martin-Subero, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
Pageof 17

Showing results (161-170 of 167) with videos related to

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Pageof 17
You have reached the last page of results.This site can display upto 167 results.
The Journal of Clinical Investigation|February 1, 2022
Targeting the ASMase/S1P pathway protects from sortilin-evoked vascular damage in hypertensionPaola Di Pietro, Albino Carrizzo, Eduardo Sommella, et al.
BMC Medical Genetics|January 25, 2013
Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetesNatalia V Rivera, Robert Carreras-Torres, Roberta Roncarati, et al.
Neurobiology of Aging|July 9, 2015
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementiaRaffaele Ferrari, Mario Grassi, Erika Salvi, et al.
Genome Research|May 27, 2011
A DNA methylation fingerprint of 1628 human samplesAgustin F Fernandez, Yassen Assenov, Jose Ignacio Martin-Subero, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
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