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Nature Reviews. Genetics
|
January 17, 2019
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact
David Monk, Deborah J G Mackay, Thomas Eggermann, et al.
Human Molecular Genetics
|
August 6, 2008
Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues
Layla Parker-Katiraee, Eleni Bousiaki, David Monk, et al.
FEMS Microbes
|
June 19, 2023
Comparability of 24-hour composite and grab samples for detection of SARS-2-CoV RNA in wastewater
Brittany L Kmush, David Monk, Hyatt Green, et al.
Human Molecular Genetics
|
July 5, 2014
Altered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placenta
Isabel Iglesias-Platas, Alex Martin-Trujillo, Paolo Petazzi, et al.
Plos Genetics
|
February 13, 2007
A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation
Andrew J Wood, Roland G Roberts, David Monk, et al.
Trends in Genetics : TIG
|
May 29, 2016
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans
Marta Sanchez-Delgado, Andrea Riccio, Thomas Eggermann, et al.
Human Molecular Genetics
|
June 3, 2009
Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression
David Monk, Philippe Arnaud, Jennifer Frost, et al.
Journal of Food Protection
|
May 25, 2019
Irradiation Inactivation of Listeria monocytogenes and Staphylococcus aureus in Low- and High-fat, Frozen and Refrigerated Ground Beef
J David Monk, Ma Rocelle S Clavero, Larry R Beuchat, et al.
Clinical Science (London, England : 1979)
|
September 11, 2016
APOA5 genetic and epigenetic variability jointly regulate circulating triacylglycerol levels
Iris Oliva, Montse Guardiola, Joan-Carles Vallvé, et al.
American Journal of Human Genetics
|
October 13, 2006
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies
Haiyan Zhou, Martin Brockington, Heinz Jungbluth, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 101) with videos related to
Sort By:
Page
of 11
Nature Reviews. Genetics
|
January 17, 2019
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact
David Monk, Deborah J G Mackay, Thomas Eggermann, et al.
Human Molecular Genetics
|
August 6, 2008
Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues
Layla Parker-Katiraee, Eleni Bousiaki, David Monk, et al.
FEMS Microbes
|
June 19, 2023
Comparability of 24-hour composite and grab samples for detection of SARS-2-CoV RNA in wastewater
Brittany L Kmush, David Monk, Hyatt Green, et al.
Human Molecular Genetics
|
July 5, 2014
Altered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placenta
Isabel Iglesias-Platas, Alex Martin-Trujillo, Paolo Petazzi, et al.
Plos Genetics
|
February 13, 2007
A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation
Andrew J Wood, Roland G Roberts, David Monk, et al.
Trends in Genetics : TIG
|
May 29, 2016
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans
Marta Sanchez-Delgado, Andrea Riccio, Thomas Eggermann, et al.
Human Molecular Genetics
|
June 3, 2009
Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression
David Monk, Philippe Arnaud, Jennifer Frost, et al.
Journal of Food Protection
|
May 25, 2019
Irradiation Inactivation of Listeria monocytogenes and Staphylococcus aureus in Low- and High-fat, Frozen and Refrigerated Ground Beef
J David Monk, Ma Rocelle S Clavero, Larry R Beuchat, et al.
Clinical Science (London, England : 1979)
|
September 11, 2016
APOA5 genetic and epigenetic variability jointly regulate circulating triacylglycerol levels
Iris Oliva, Montse Guardiola, Joan-Carles Vallvé, et al.
American Journal of Human Genetics
|
October 13, 2006
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies
Haiyan Zhou, Martin Brockington, Heinz Jungbluth, et al.
Page
of 11