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Paolo Manunta

Showing results (131-140 of 146) with videos related to

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Hypertension (Dallas, Tex. : 1979)|September 11, 2013
Target sequencing, cell experiments, and a population study establish endothelial nitric oxide synthase (eNOS) gene as hypertension susceptibility geneErika Salvi, Tatiana Kuznetsova, Lutgarde Thijs, et al.
Diabetes, Obesity & Metabolism|February 23, 2019
Effects of valsartan, benazepril and their combination in overt nephropathy of type 2 diabetes: A prospective, randomized, controlled trialPiero Ruggenenti, Matias Trillini, Drazenka P Barlovic, et al.
Hypertension (Dallas, Tex. : 1979)|November 2, 2016
Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to HydrochlorothiazideErika Salvi, Zhiying Wang, Federica Rizzi, et al.
Hypertension (Dallas, Tex. : 1979)|June 12, 2013
Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazideStephen T Turner, Eric Boerwinkle, Jeffrey R O'Connell, 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.
Journal of Hypertension|February 20, 2015
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensivesMartina Chittani, Roberta Zaninello, Chiara Lanzani, et al.
Pharmacogenomics|November 21, 2014
Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA studyFrancesca Frau, Roberta Zaninello, Erika Salvi, et al.
Hypertension (Dallas, Tex. : 1979)|December 21, 2011
Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthaseErika Salvi, Zoltán Kutalik, Nicola Glorioso, et al.
The American Journal of Psychiatry|August 27, 2014
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCDDongmei Yu, Carol A Mathews, Jeremiah M Scharf, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
Pageof 15

Showing results (131-140 of 146) with videos related to

Sort By:
Pageof 15
Hypertension (Dallas, Tex. : 1979)|September 11, 2013
Target sequencing, cell experiments, and a population study establish endothelial nitric oxide synthase (eNOS) gene as hypertension susceptibility geneErika Salvi, Tatiana Kuznetsova, Lutgarde Thijs, et al.
Diabetes, Obesity & Metabolism|February 23, 2019
Effects of valsartan, benazepril and their combination in overt nephropathy of type 2 diabetes: A prospective, randomized, controlled trialPiero Ruggenenti, Matias Trillini, Drazenka P Barlovic, et al.
Hypertension (Dallas, Tex. : 1979)|November 2, 2016
Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to HydrochlorothiazideErika Salvi, Zhiying Wang, Federica Rizzi, et al.
Hypertension (Dallas, Tex. : 1979)|June 12, 2013
Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazideStephen T Turner, Eric Boerwinkle, Jeffrey R O'Connell, 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.
Journal of Hypertension|February 20, 2015
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensivesMartina Chittani, Roberta Zaninello, Chiara Lanzani, et al.
Pharmacogenomics|November 21, 2014
Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA studyFrancesca Frau, Roberta Zaninello, Erika Salvi, et al.
Hypertension (Dallas, Tex. : 1979)|December 21, 2011
Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthaseErika Salvi, Zoltán Kutalik, Nicola Glorioso, et al.
The American Journal of Psychiatry|August 27, 2014
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCDDongmei Yu, Carol A Mathews, Jeremiah M Scharf, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
Pageof 15