Search research articles
Contact Us
Filters
Showing results (1-10 of 25) with videos related to
Page
of 3
Sort By:
Nucleic Acids Research
|
February 12, 2008
Cell-free cloning of highly expanded CTG repeats by amplification of dimerized expanded repeats
Robert J Osborne, Charles A Thornton
Human Molecular Genetics
|
September 22, 2006
RNA-dominant diseases
Robert J Osborne, Charles A Thornton
Molecular Vision
|
December 16, 2011
Parent-of-origin effects in SOX2 anophthalmia syndrome
Robert 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 anomalies
Alexander 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 sequencing
James 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 DNAs
James 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 dystrophy
Robert 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 RNA
Thurman 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 CLCN1
John 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 dystrophy
Hongqing Du, Melissa S Cline, Robert J Osborne, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Nucleic Acids Research
|
February 12, 2008
Cell-free cloning of highly expanded CTG repeats by amplification of dimerized expanded repeats
Robert J Osborne, Charles A Thornton
Human Molecular Genetics
|
September 22, 2006
RNA-dominant diseases
Robert J Osborne, Charles A Thornton
Molecular Vision
|
December 16, 2011
Parent-of-origin effects in SOX2 anophthalmia syndrome
Robert 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 anomalies
Alexander 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 sequencing
James 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 DNAs
James 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 dystrophy
Robert 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 RNA
Thurman 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 CLCN1
John 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 dystrophy
Hongqing Du, Melissa S Cline, Robert J Osborne, et al.
Page
of 3