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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 hypothesis
R 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 barcodes
Megan L McCloskey, Reinhard Stöger, R Scott Hansen, et al.
Nucleic Acids Research
|
October 2, 2004
Molecular barcodes detect redundancy and contamination in hairpin-bisulfite PCR
Brooks 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 cultures
Stanley 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 arrest
Holly Brunton, Aaron A Goodarzi, Angela T Noon, et al.
Plos Genetics
|
December 10, 2009
Dosage regulation of the active X chromosome in human triploid cells
Xinxian 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 proteins
Stanley 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 elements
Alice 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 activity
Jimena V Goldstine, Shareef Nahas, Kristin Gamo, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 26) with videos related to
Sort By:
Page
of 3
Human Molecular Genetics
|
August 20, 2003
X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis
R 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 barcodes
Megan L McCloskey, Reinhard Stöger, R Scott Hansen, et al.
Nucleic Acids Research
|
October 2, 2004
Molecular barcodes detect redundancy and contamination in hairpin-bisulfite PCR
Brooks 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 cultures
Stanley 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 arrest
Holly Brunton, Aaron A Goodarzi, Angela T Noon, et al.
Plos Genetics
|
December 10, 2009
Dosage regulation of the active X chromosome in human triploid cells
Xinxian 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 proteins
Stanley 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 elements
Alice 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 activity
Jimena V Goldstine, Shareef Nahas, Kristin Gamo, et al.
Page
of 3