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Robert J Osborne

Showing results (1-10 of 25) with videos related to

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Nucleic Acids Research|February 12, 2008
Cell-free cloning of highly expanded CTG repeats by amplification of dimerized expanded repeatsRobert J Osborne, Charles A Thornton
Human Molecular Genetics|September 22, 2006
RNA-dominant diseasesRobert J Osborne, Charles A Thornton
Molecular Vision|December 16, 2011
Parent-of-origin effects in SOX2 anophthalmia syndromeRobert J Osborne, Jennifer J Kurinczuk, Nicola K Ragge
Human Mutation|May 28, 2010
Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomaliesAlexander W Wyatt, Robert J Osborne, Helen Stewart, et al.
Nucleic Acids Research|April 15, 2011
A method for counting PCR template molecules with application to next-generation sequencingJames A Casbon, Robert J Osborne, Sydney Brenner, et al.
Nucleic Acids Research|April 13, 2013
Reflex: intramolecular barcoding of long-range PCR products for sequencing multiple pooled DNAsJames A Casbon, Andrew F Slatter, Esther Musgrave-Brown, et al.
Human Molecular Genetics|February 19, 2009
Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophyRobert J Osborne, Xiaoyan Lin, Stephen Welle, et al.
Science (New York, N.Y.)|July 18, 2009
Reversal of RNA dominance by displacement of protein sequestered on triplet repeat RNAThurman M Wheeler, Krzysztof Sobczak, John D Lueck, et al.
American Journal of Physiology. Cell Physiology|December 1, 2006
Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1John D Lueck, Codrin Lungu, Ami Mankodi, et al.
Nature Structural & Molecular Biology|January 26, 2010
Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophyHongqing Du, Melissa S Cline, Robert J Osborne, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Nucleic Acids Research|February 12, 2008
Cell-free cloning of highly expanded CTG repeats by amplification of dimerized expanded repeatsRobert J Osborne, Charles A Thornton
Human Molecular Genetics|September 22, 2006
RNA-dominant diseasesRobert J Osborne, Charles A Thornton
Molecular Vision|December 16, 2011
Parent-of-origin effects in SOX2 anophthalmia syndromeRobert J Osborne, Jennifer J Kurinczuk, Nicola K Ragge
Human Mutation|May 28, 2010
Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomaliesAlexander W Wyatt, Robert J Osborne, Helen Stewart, et al.
Nucleic Acids Research|April 15, 2011
A method for counting PCR template molecules with application to next-generation sequencingJames A Casbon, Robert J Osborne, Sydney Brenner, et al.
Nucleic Acids Research|April 13, 2013
Reflex: intramolecular barcoding of long-range PCR products for sequencing multiple pooled DNAsJames A Casbon, Andrew F Slatter, Esther Musgrave-Brown, et al.
Human Molecular Genetics|February 19, 2009
Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophyRobert J Osborne, Xiaoyan Lin, Stephen Welle, et al.
Science (New York, N.Y.)|July 18, 2009
Reversal of RNA dominance by displacement of protein sequestered on triplet repeat RNAThurman M Wheeler, Krzysztof Sobczak, John D Lueck, et al.
American Journal of Physiology. Cell Physiology|December 1, 2006
Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1John D Lueck, Codrin Lungu, Ami Mankodi, et al.
Nature Structural & Molecular Biology|January 26, 2010
Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophyHongqing Du, Melissa S Cline, Robert J Osborne, et al.
Pageof 3