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Expert Review of Molecular Diagnostics
|
July 24, 2015
The role of clinical genomic testing in diagnosis and discovery of pathogenic mutations
Peter L Nagy, Mahesh Mansukhani
Wiley Interdisciplinary Reviews. Systems Biology and Medicine
|
January 5, 2010
Formaldehyde-assisted isolation of regulatory elements
Peter L Nagy, David H Price
Methods in Molecular Biology (Clifton, N.J.)
|
August 25, 2018
Next-Generation Sequencing and Mutational Analysis: Implications for Genes Encoding LINC Complex Proteins
Peter L Nagy, Howard J Worman
American Journal of Medical Genetics. Part A
|
July 16, 2024
Optical genome mapping with genome sequencing identifies subtelomeric Xq28 deletion and inserted 7p22.3 duplication in a male with multisystem developmental disorder
Jorge L Rodriguez-Gil, Peter L Nagy, Uta Francke
Mutation Research
|
November 6, 2008
Editorial. Epigenetics of development and human disease
Lori L Wallrath, Peter L Nagy, Pamela K Geyer
Proceedings of the National Academy of Sciences of the United States of America
|
December 26, 2001
A trithorax-group complex purified from Saccharomyces cerevisiae is required for methylation of histone H3
Peter L Nagy, Joachim Griesenbeck, Roger D Kornberg, et al.
Disease Models & Mechanisms
|
August 4, 2011
LMNA cardiomyopathy: cell biology and genetics meet clinical medicine
Jonathan T Lu, Antoine Muchir, Peter L Nagy, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 17, 2003
Genomewide demarcation of RNA polymerase II transcription units revealed by physical fractionation of chromatin
Peter L Nagy, Michael L Cleary, Patrick O Brown, et al.
Molecular Syndromology
|
February 26, 2019
Clinical Transcriptome Sequencing Confirms Activation of a Cryptic Splice Site in Suspected <i>SYNGAP1</i>-Related Disorder
Elise Brimble, Christopher Lee-Messer, Peter L Nagy, et al.
The Journal of Clinical Investigation
|
May 8, 2002
Male infertility, impaired spermatogenesis, and azoospermia in mice deficient for the pseudophosphatase Sbf1
Ron Firestein, Peter L Nagy, Megan Daly, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
Expert Review of Molecular Diagnostics
|
July 24, 2015
The role of clinical genomic testing in diagnosis and discovery of pathogenic mutations
Peter L Nagy, Mahesh Mansukhani
Wiley Interdisciplinary Reviews. Systems Biology and Medicine
|
January 5, 2010
Formaldehyde-assisted isolation of regulatory elements
Peter L Nagy, David H Price
Methods in Molecular Biology (Clifton, N.J.)
|
August 25, 2018
Next-Generation Sequencing and Mutational Analysis: Implications for Genes Encoding LINC Complex Proteins
Peter L Nagy, Howard J Worman
American Journal of Medical Genetics. Part A
|
July 16, 2024
Optical genome mapping with genome sequencing identifies subtelomeric Xq28 deletion and inserted 7p22.3 duplication in a male with multisystem developmental disorder
Jorge L Rodriguez-Gil, Peter L Nagy, Uta Francke
Mutation Research
|
November 6, 2008
Editorial. Epigenetics of development and human disease
Lori L Wallrath, Peter L Nagy, Pamela K Geyer
Proceedings of the National Academy of Sciences of the United States of America
|
December 26, 2001
A trithorax-group complex purified from Saccharomyces cerevisiae is required for methylation of histone H3
Peter L Nagy, Joachim Griesenbeck, Roger D Kornberg, et al.
Disease Models & Mechanisms
|
August 4, 2011
LMNA cardiomyopathy: cell biology and genetics meet clinical medicine
Jonathan T Lu, Antoine Muchir, Peter L Nagy, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 17, 2003
Genomewide demarcation of RNA polymerase II transcription units revealed by physical fractionation of chromatin
Peter L Nagy, Michael L Cleary, Patrick O Brown, et al.
Molecular Syndromology
|
February 26, 2019
Clinical Transcriptome Sequencing Confirms Activation of a Cryptic Splice Site in Suspected <i>SYNGAP1</i>-Related Disorder
Elise Brimble, Christopher Lee-Messer, Peter L Nagy, et al.
The Journal of Clinical Investigation
|
May 8, 2002
Male infertility, impaired spermatogenesis, and azoospermia in mice deficient for the pseudophosphatase Sbf1
Ron Firestein, Peter L Nagy, Megan Daly, et al.
Page
of 5