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Alan F Wright

Showing results (81-90 of 239) with videos related to

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BMC Genomics|February 27, 2010
Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic dataOzren Polasek, Caroline Hayward, Celine Bellenguez, et al.
Genetic Epidemiology|August 22, 2009
Genetic comparison of a Croatian isolate and CEPH European foundersPau Navarro, Véronique Vitart, Caroline Hayward, et al.
European Journal of Human Genetics : EJHG|January 31, 2013
Inference of identity by descent in population isolates and optimal sequencing studiesDominik Glodzik, Pau Navarro, Veronique Vitart, et al.
Immunobiology|October 26, 2011
Genetic variation in complement regulators and susceptibility to age-related macular degenerationValentina Cipriani, Baljinder K Matharu, Jane C Khan, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degenerationAnn H Milam, Linda Rose, Artur V Cideciyan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 4, 2011
Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2Dganit Dinour, Nicola K Gray, Liat Ganon, et al.
Human Molecular Genetics|March 4, 2010
Variation in the uric acid transporter gene (SLC2A9) and memory performanceLorna M Houlihan, Niki D Wyatt, Sarah E Harris, et al.
American Journal of Hypertension|March 7, 2009
A quantitative trait locus for SBP maps near KCNB1 and PTGIS in a population isolateMaja Barbalić, Nina Smolej Narancić, Tatjana Skarić-Jurić, et al.
Plos One|October 19, 2012
Localising loci underlying complex trait variation using Regional Genomic Relationship MappingYoshitaka Nagamine, Ricardo Pong-Wong, Pau Navarro, et al.
Pageof 24

Showing results (81-90 of 239) with videos related to

Sort By:
Pageof 24
BMC Genomics|February 27, 2010
Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic dataOzren Polasek, Caroline Hayward, Celine Bellenguez, et al.
Genetic Epidemiology|August 22, 2009
Genetic comparison of a Croatian isolate and CEPH European foundersPau Navarro, Véronique Vitart, Caroline Hayward, et al.
European Journal of Human Genetics : EJHG|January 31, 2013
Inference of identity by descent in population isolates and optimal sequencing studiesDominik Glodzik, Pau Navarro, Veronique Vitart, et al.
Immunobiology|October 26, 2011
Genetic variation in complement regulators and susceptibility to age-related macular degenerationValentina Cipriani, Baljinder K Matharu, Jane C Khan, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degenerationAnn H Milam, Linda Rose, Artur V Cideciyan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 4, 2011
Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2Dganit Dinour, Nicola K Gray, Liat Ganon, et al.
Human Molecular Genetics|March 4, 2010
Variation in the uric acid transporter gene (SLC2A9) and memory performanceLorna M Houlihan, Niki D Wyatt, Sarah E Harris, et al.
American Journal of Hypertension|March 7, 2009
A quantitative trait locus for SBP maps near KCNB1 and PTGIS in a population isolateMaja Barbalić, Nina Smolej Narancić, Tatjana Skarić-Jurić, et al.
Plos One|October 19, 2012
Localising loci underlying complex trait variation using Regional Genomic Relationship MappingYoshitaka Nagamine, Ricardo Pong-Wong, Pau Navarro, et al.
Pageof 24