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Stanley F Nelson

Showing results (41-50 of 256) with videos related to

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Human Molecular Genetics|February 7, 2014
Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivationHane Lee, Meng-chin A Lin, Harley I Kornblum, et al.
Neurogenetics|July 5, 2007
Association of progesterone receptor with migraine-associated vertigoHane Lee, Lauren Sininger, Joanna C Jen, et al.
BMC Genomics|March 7, 2006
Gene connectivity, function, and sequence conservation: predictions from modular yeast co-expression networksMarc R J Carlson, Bin Zhang, Zixing Fang, et al.
BMC Medical Genetics|January 22, 2014
Whole exome sequencing detects homozygosity for ABCA4 p.Arg602Trp missense mutation in a pediatric patient with rapidly progressive retinal dystrophyMaria Carolina Ortube, Samuel P Strom, Stanley F Nelson, et al.
Human Mutation|August 19, 2007
Representational oligonucleotide microarray analysis (ROMA) and comparison of binning and change-point methods of analysis: application to detection of del22q11.2 (DiGeorge) syndromeChristopher M Stanczak, Zugen Chen, Stanley F Nelson, et al.
Journal of Lipid Research|October 28, 2005
FXR regulates organic solute transporters alpha and beta in the adrenal gland, kidney, and intestineHans Lee, Yanqiao Zhang, Florence Y Lee, et al.
Frontiers in Cardiovascular Medicine|June 17, 2017
A Path to Implement Precision Child Health Cardiovascular MedicineMarlin Touma, Brian Reemtsen, Nancy Halnon, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 8, 2008
Genetically defined EWS/FLI1 model system suggests mesenchymal origin of Ewing's family tumorsGary Potikyan, Kelly A France, Marc R J Carlson, et al.
BMC Cancer|September 20, 2008
Expression profile of CREB knockdown in myeloid leukemia cellsMatteo Pellegrini, Jerry C Cheng, Jon Voutila, et al.
American Journal of Medical Genetics. Part A|February 7, 2014
X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblingsNesrine Bissar-Tadmouri, Whithey L Donahue, Lihadh Al-Gazali, et al.
Pageof 26

Showing results (41-50 of 256) with videos related to

Sort By:
Pageof 26
Human Molecular Genetics|February 7, 2014
Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivationHane Lee, Meng-chin A Lin, Harley I Kornblum, et al.
Neurogenetics|July 5, 2007
Association of progesterone receptor with migraine-associated vertigoHane Lee, Lauren Sininger, Joanna C Jen, et al.
BMC Genomics|March 7, 2006
Gene connectivity, function, and sequence conservation: predictions from modular yeast co-expression networksMarc R J Carlson, Bin Zhang, Zixing Fang, et al.
BMC Medical Genetics|January 22, 2014
Whole exome sequencing detects homozygosity for ABCA4 p.Arg602Trp missense mutation in a pediatric patient with rapidly progressive retinal dystrophyMaria Carolina Ortube, Samuel P Strom, Stanley F Nelson, et al.
Human Mutation|August 19, 2007
Representational oligonucleotide microarray analysis (ROMA) and comparison of binning and change-point methods of analysis: application to detection of del22q11.2 (DiGeorge) syndromeChristopher M Stanczak, Zugen Chen, Stanley F Nelson, et al.
Journal of Lipid Research|October 28, 2005
FXR regulates organic solute transporters alpha and beta in the adrenal gland, kidney, and intestineHans Lee, Yanqiao Zhang, Florence Y Lee, et al.
Frontiers in Cardiovascular Medicine|June 17, 2017
A Path to Implement Precision Child Health Cardiovascular MedicineMarlin Touma, Brian Reemtsen, Nancy Halnon, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 8, 2008
Genetically defined EWS/FLI1 model system suggests mesenchymal origin of Ewing's family tumorsGary Potikyan, Kelly A France, Marc R J Carlson, et al.
BMC Cancer|September 20, 2008
Expression profile of CREB knockdown in myeloid leukemia cellsMatteo Pellegrini, Jerry C Cheng, Jon Voutila, et al.
American Journal of Medical Genetics. Part A|February 7, 2014
X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblingsNesrine Bissar-Tadmouri, Whithey L Donahue, Lihadh Al-Gazali, et al.
Pageof 26