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Alan F Wright

Showing results (101-110 of 239) with videos related to

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Journal of the American Society of Nephrology : JASN|November 21, 2009
Homozygous SLC2A9 mutations cause severe renal hypouricemiaDganit Dinour, Nicola K Gray, Susan Campbell, et al.
Scientific Reports|September 24, 2017
Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degenerationChloe M Stanton, Shyamanga Borooah, Camilla Drake, et al.
Epigenetics|March 8, 2012
Epigenetic silencing of HNF1A associates with changes in the composition of the human plasma N-glycomeVlatka Zoldoš, Tomislav Horvat, Mislav Novokmet, et al.
Investigative Ophthalmology & Visual Science|December 22, 2023
Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5Randa T H Li, Alejandro J Roman, Alexander Sumaroka, et al.
European Journal of Human Genetics : EJHG|October 13, 2011
No evidence of association between complement factor I genetic variant rs10033900 and age-related macular degenerationValentina Cipriani, Baljinder K Matharu, Jane C Khan, et al.
Croatian Medical Journal|March 5, 2009
Historic, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemicsZrinka Biloglav, Lina Zgaga, Mladen Smoljanović, et al.
Plos One|July 23, 2013
Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studiesPeter K Joshi, James Prendergast, Ross M Fraser, et al.
European Journal of Human Genetics : EJHG|April 7, 2016
Whole-exome sequencing in an isolated population from the Dalmatian island of VisAna Jeroncic, Yasin Memari, Graham Rs Ritchie, et al.
Journal of Medical Genetics|April 16, 2011
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathwaysGiorgia Girotto, Nicola Pirastu, Rossella Sorice, et al.
Intelligence|June 20, 2014
Molecular genetic contributions to socioeconomic status and intelligenceRiccardo E Marioni, Gail Davies, Caroline Hayward, et al.
Pageof 24

Showing results (101-110 of 239) with videos related to

Sort By:
Pageof 24
Journal of the American Society of Nephrology : JASN|November 21, 2009
Homozygous SLC2A9 mutations cause severe renal hypouricemiaDganit Dinour, Nicola K Gray, Susan Campbell, et al.
Scientific Reports|September 24, 2017
Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degenerationChloe M Stanton, Shyamanga Borooah, Camilla Drake, et al.
Epigenetics|March 8, 2012
Epigenetic silencing of HNF1A associates with changes in the composition of the human plasma N-glycomeVlatka Zoldoš, Tomislav Horvat, Mislav Novokmet, et al.
Investigative Ophthalmology & Visual Science|December 22, 2023
Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5Randa T H Li, Alejandro J Roman, Alexander Sumaroka, et al.
European Journal of Human Genetics : EJHG|October 13, 2011
No evidence of association between complement factor I genetic variant rs10033900 and age-related macular degenerationValentina Cipriani, Baljinder K Matharu, Jane C Khan, et al.
Croatian Medical Journal|March 5, 2009
Historic, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemicsZrinka Biloglav, Lina Zgaga, Mladen Smoljanović, et al.
Plos One|July 23, 2013
Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studiesPeter K Joshi, James Prendergast, Ross M Fraser, et al.
European Journal of Human Genetics : EJHG|April 7, 2016
Whole-exome sequencing in an isolated population from the Dalmatian island of VisAna Jeroncic, Yasin Memari, Graham Rs Ritchie, et al.
Journal of Medical Genetics|April 16, 2011
Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathwaysGiorgia Girotto, Nicola Pirastu, Rossella Sorice, et al.
Intelligence|June 20, 2014
Molecular genetic contributions to socioeconomic status and intelligenceRiccardo E Marioni, Gail Davies, Caroline Hayward, et al.
Pageof 24