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R Scott Hansen

Showing results (1-10 of 26) with videos related to

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Human Molecular Genetics|August 20, 2003
X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesisR Scott Hansen
Nature Medicine|November 2, 2002
A new regulatory pathway for fragile X syndrome?R Scott Hansen, Charles D Laird
Biochemical Genetics|October 24, 2007
Encoding PCR products with batch-stamps and barcodesMegan L McCloskey, Reinhard Stöger, R Scott Hansen, et al.
Nucleic Acids Research|October 2, 2004
Molecular barcodes detect redundancy and contamination in hairpin-bisulfite PCRBrooks E Miner, Reinhard J Stöger, Alice F Burden, et al.
BMC Genetics|July 5, 2006
Abnormal X: autosome ratio, but normal X chromosome inactivation in human triploid culturesStanley M Gartler, Kartik R Varadarajan, Ping Luo, et al.
Molecular and Cellular Biology|July 28, 2011
Analysis of human syndromes with disordered chromatin reveals the impact of heterochromatin on the efficacy of ATM-dependent G2/M checkpoint arrestHolly Brunton, Aaron A Goodarzi, Angela T Noon, et al.
Plos Genetics|December 10, 2009
Dosage regulation of the active X chromosome in human triploid cellsXinxian Deng, Di Kim Nguyen, R Scott Hansen, et al.
BMC Biology|September 21, 2004
Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteinsStanley M Gartler, Kartik R Varadarajan, Ping Luo, et al.
The Journal of Biological Chemistry|February 16, 2005
Hemimethylation and non-CpG methylation levels in a promoter region of human LINE-1 (L1) repeated elementsAlice F Burden, Nathan C Manley, Aaron D Clark, et al.
DNA Repair|January 24, 2006
Constitutive phosphorylation of ATM in lymphoblastoid cell lines from patients with ICF syndrome without downstream kinase activityJimena V Goldstine, Shareef Nahas, Kristin Gamo, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|August 20, 2003
X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesisR Scott Hansen
Nature Medicine|November 2, 2002
A new regulatory pathway for fragile X syndrome?R Scott Hansen, Charles D Laird
Biochemical Genetics|October 24, 2007
Encoding PCR products with batch-stamps and barcodesMegan L McCloskey, Reinhard Stöger, R Scott Hansen, et al.
Nucleic Acids Research|October 2, 2004
Molecular barcodes detect redundancy and contamination in hairpin-bisulfite PCRBrooks E Miner, Reinhard J Stöger, Alice F Burden, et al.
BMC Genetics|July 5, 2006
Abnormal X: autosome ratio, but normal X chromosome inactivation in human triploid culturesStanley M Gartler, Kartik R Varadarajan, Ping Luo, et al.
Molecular and Cellular Biology|July 28, 2011
Analysis of human syndromes with disordered chromatin reveals the impact of heterochromatin on the efficacy of ATM-dependent G2/M checkpoint arrestHolly Brunton, Aaron A Goodarzi, Angela T Noon, et al.
Plos Genetics|December 10, 2009
Dosage regulation of the active X chromosome in human triploid cellsXinxian Deng, Di Kim Nguyen, R Scott Hansen, et al.
BMC Biology|September 21, 2004
Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteinsStanley M Gartler, Kartik R Varadarajan, Ping Luo, et al.
The Journal of Biological Chemistry|February 16, 2005
Hemimethylation and non-CpG methylation levels in a promoter region of human LINE-1 (L1) repeated elementsAlice F Burden, Nathan C Manley, Aaron D Clark, et al.
DNA Repair|January 24, 2006
Constitutive phosphorylation of ATM in lymphoblastoid cell lines from patients with ICF syndrome without downstream kinase activityJimena V Goldstine, Shareef Nahas, Kristin Gamo, et al.
Pageof 3