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David J Cutler

Showing results (61-70 of 142) with videos related to

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JAMA Neurology|May 29, 2019
Association of Early-Onset Alzheimer Disease With Elevated Low-Density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOBThomas S Wingo, David J Cutler, Aliza P Wingo, et al.
JIMD Reports|February 15, 2015
A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic GalactosemiaThanh-Thanh Claire V Tran, Ying Liu, Michael E Zwick, et al.
Open Access Bioinformatics|March 8, 2011
Microarray oligonucleotide probe designer (MOPeD): A web serviceViren C Patel, Kajari Mondal, Amol Carl Shetty, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 30, 2022
LDL cholesterol is associated with higher AD neuropathology burden independent of APOEAliza P Wingo, Selina M Vattathil, Jiaqi Liu, et al.
Plos Genetics|July 31, 2007
Population bottlenecks as a potential major shaping force of human genome architectureAdrian Gherman, Peter E Chen, Tanya M Teslovich, et al.
Journal of Proteome Research|July 11, 2017
Integrating Next-Generation Genomic Sequencing and Mass Spectrometry To Estimate Allele-Specific Protein Abundance in Human BrainThomas S Wingo, Duc M Duong, Maotian Zhou, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizesH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencingH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
The European Journal of Neuroscience|January 25, 2003
The mouse VPAC2 receptor confers suprachiasmatic nuclei cellular rhythmicity and responsiveness to vasoactive intestinal polypeptide in vitroDavid J Cutler, Mai Haraura, Helen E Reed, et al.
Plos One|March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotypeStephen C Collins, Brad Coffee, Paul J Benke, et al.
Pageof 15

Showing results (61-70 of 142) with videos related to

Sort By:
Pageof 15
JAMA Neurology|May 29, 2019
Association of Early-Onset Alzheimer Disease With Elevated Low-Density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOBThomas S Wingo, David J Cutler, Aliza P Wingo, et al.
JIMD Reports|February 15, 2015
A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic GalactosemiaThanh-Thanh Claire V Tran, Ying Liu, Michael E Zwick, et al.
Open Access Bioinformatics|March 8, 2011
Microarray oligonucleotide probe designer (MOPeD): A web serviceViren C Patel, Kajari Mondal, Amol Carl Shetty, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 30, 2022
LDL cholesterol is associated with higher AD neuropathology burden independent of APOEAliza P Wingo, Selina M Vattathil, Jiaqi Liu, et al.
Plos Genetics|July 31, 2007
Population bottlenecks as a potential major shaping force of human genome architectureAdrian Gherman, Peter E Chen, Tanya M Teslovich, et al.
Journal of Proteome Research|July 11, 2017
Integrating Next-Generation Genomic Sequencing and Mass Spectrometry To Estimate Allele-Specific Protein Abundance in Human BrainThomas S Wingo, Duc M Duong, Maotian Zhou, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizesH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencingH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
The European Journal of Neuroscience|January 25, 2003
The mouse VPAC2 receptor confers suprachiasmatic nuclei cellular rhythmicity and responsiveness to vasoactive intestinal polypeptide in vitroDavid J Cutler, Mai Haraura, Helen E Reed, et al.
Plos One|March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotypeStephen C Collins, Brad Coffee, Paul J Benke, et al.
Pageof 15