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Penny J Norsworthy

Showing results (1-10 of 11) with videos related to

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Disease Models & Mechanisms|January 29, 2017
Genetic, physiological and comparative genomic studies of hypertension and insulin resistance in the spontaneously hypertensive ratPhilip M Coan, Oliver Hummel, Ana Garcia Diaz, et al.
Experimental Nephrology|October 17, 2002
Segregation of experimental autoimmune glomerulonephritis as a complex genetic trait and exclusion of Col4a3 as a candidate geneJohn Reynolds, Paul R Cook, James J Ryan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 17, 2002
Radiation hybrid mapping of 70 rat genes from a data set of differentially expressed genesCaroline A Wallace, Saira Ali, Anne M Glazier, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemiaEllen R A Thomas, Santosh S Atanur, Penny J Norsworthy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 18, 2013
The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemiaJana Vandrovcova, Ellen R A Thomas, Santosh S Atanur, et al.
Nature Communications|August 10, 2020
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosisPenny J Norsworthy, Andrew G B Thompson, Tze H Mok, et al.
BMC Medical Genetics|June 25, 2014
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based studyPenny J Norsworthy, Jana Vandrovcova, Ellen R A Thomas, et al.
Plos Genetics|December 5, 2014
Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular diseaseMichelle D Johnson, Michael Mueller, Martyna Adamowicz-Brice, et al.
Nature|February 17, 2006
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humansTimothy J Aitman, Rong Dong, Timothy J Vyse, et al.
Nature Genetics|May 29, 2007
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunityManuela Fanciulli, Penny J Norsworthy, Enrico Petretto, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Disease Models & Mechanisms|January 29, 2017
Genetic, physiological and comparative genomic studies of hypertension and insulin resistance in the spontaneously hypertensive ratPhilip M Coan, Oliver Hummel, Ana Garcia Diaz, et al.
Experimental Nephrology|October 17, 2002
Segregation of experimental autoimmune glomerulonephritis as a complex genetic trait and exclusion of Col4a3 as a candidate geneJohn Reynolds, Paul R Cook, James J Ryan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 17, 2002
Radiation hybrid mapping of 70 rat genes from a data set of differentially expressed genesCaroline A Wallace, Saira Ali, Anne M Glazier, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemiaEllen R A Thomas, Santosh S Atanur, Penny J Norsworthy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 18, 2013
The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemiaJana Vandrovcova, Ellen R A Thomas, Santosh S Atanur, et al.
Nature Communications|August 10, 2020
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosisPenny J Norsworthy, Andrew G B Thompson, Tze H Mok, et al.
BMC Medical Genetics|June 25, 2014
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based studyPenny J Norsworthy, Jana Vandrovcova, Ellen R A Thomas, et al.
Plos Genetics|December 5, 2014
Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular diseaseMichelle D Johnson, Michael Mueller, Martyna Adamowicz-Brice, et al.
Nature|February 17, 2006
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humansTimothy J Aitman, Rong Dong, Timothy J Vyse, et al.
Nature Genetics|May 29, 2007
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunityManuela Fanciulli, Penny J Norsworthy, Enrico Petretto, et al.
Pageof 2