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Roger H Reeves

Showing results (71-80 of 92) with videos related to

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Journal of Neurodevelopmental Disorders|April 20, 2021
Capturing cognitive and behavioral variability among individuals with Down syndrome: a latent profile analysisMarie Moore Channell, Laura J Mattie, Debra R Hamilton, et al.
Japanese Journal of Cancer Research : Gann|June 25, 2002
Promoter methylation of TSLC1 and tumor suppression by its gene product in human prostate cancerHiroshi Fukuhara, Masami Kuramochi, Takeshi Fukami, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Hypermetabolism in mice carrying a near complete human chromosome 21Dylan C Sarver, Cheng Xu, Susana Rodriguez, et al.
Elife|May 30, 2023
Hypermetabolism in mice carrying a near-complete human chromosome 21Dylan C Sarver, Cheng Xu, Susana Rodriguez, et al.
Genome Research|July 3, 2004
Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndromePascal Kahlem, Marc Sultan, Ralf Herwig, et al.
Human Molecular Genetics|June 25, 2016
Cilia gene mutations cause atrioventricular septal defects by multiple mechanismsOzanna Burnicka-Turek, Jeffrey D Steimle, Wenhui Huang, et al.
American Journal of Human Genetics|October 9, 2012
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defectsChristine Ackerman, Adam E Locke, Eleanor Feingold, et al.
American Journal on Intellectual and Developmental Disabilities|April 29, 2017
The Arizona Cognitive Test Battery for Down Syndrome: Test-Retest Reliability and Practice EffectsJamie O Edgin, Payal Anand, Tracie Rosser, et al.
G3 (Bethesda, Md.)|November 17, 2017
Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart DefectsBenjamin L Rambo-Martin, Jennifer G Mulle, David J Cutler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2014
Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defectsDhanya Ramachandran, Jennifer G Mulle, Adam E Locke, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Journal of Neurodevelopmental Disorders|April 20, 2021
Capturing cognitive and behavioral variability among individuals with Down syndrome: a latent profile analysisMarie Moore Channell, Laura J Mattie, Debra R Hamilton, et al.
Japanese Journal of Cancer Research : Gann|June 25, 2002
Promoter methylation of TSLC1 and tumor suppression by its gene product in human prostate cancerHiroshi Fukuhara, Masami Kuramochi, Takeshi Fukami, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Hypermetabolism in mice carrying a near complete human chromosome 21Dylan C Sarver, Cheng Xu, Susana Rodriguez, et al.
Elife|May 30, 2023
Hypermetabolism in mice carrying a near-complete human chromosome 21Dylan C Sarver, Cheng Xu, Susana Rodriguez, et al.
Genome Research|July 3, 2004
Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndromePascal Kahlem, Marc Sultan, Ralf Herwig, et al.
Human Molecular Genetics|June 25, 2016
Cilia gene mutations cause atrioventricular septal defects by multiple mechanismsOzanna Burnicka-Turek, Jeffrey D Steimle, Wenhui Huang, et al.
American Journal of Human Genetics|October 9, 2012
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defectsChristine Ackerman, Adam E Locke, Eleanor Feingold, et al.
American Journal on Intellectual and Developmental Disabilities|April 29, 2017
The Arizona Cognitive Test Battery for Down Syndrome: Test-Retest Reliability and Practice EffectsJamie O Edgin, Payal Anand, Tracie Rosser, et al.
G3 (Bethesda, Md.)|November 17, 2017
Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart DefectsBenjamin L Rambo-Martin, Jennifer G Mulle, David J Cutler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2014
Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defectsDhanya Ramachandran, Jennifer G Mulle, Adam E Locke, et al.
Pageof 10