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David Monk

Showing results (71-80 of 101) with videos related to

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Nucleic Acids Research|February 9, 2011
Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genesDavid Monk, Philippe Arnaud, Jennifer M Frost, et al.
Human Mutation|March 4, 2017
Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprintedMiguel Alsina Casanova, Ana Monteagudo-Sánchez, Luciana Rodiguez Guerineau, et al.
Neurology|June 19, 2016
Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 familiesAnne S Soehn, Tim W Rattay, Stefanie Beck-Wödl, et al.
Nucleic Acids Research|October 14, 2020
The role of ZFP57 and additional KRAB-zinc finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbancesAna Monteagudo-Sánchez, Jose Ramon Hernandez Mora, Carlos Simon, et al.
Epigenetics|June 26, 2025
<i>PIK3R1</i> and <i>G0S2</i> are human placenta-specific imprinted genes associated with germline-inherited maternal DNA methylationDagne Daskeviciute, Becky Sainty, Louise Chappell-Maor, et al.
Nature Medicine|May 9, 2018
PM20D1 is a quantitative trait locus associated with Alzheimer's diseaseJose V Sanchez-Mut, Holger Heyn, Bianca A Silva, et al.
Plos Genetics|November 12, 2016
Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient ImprintingMarta Sanchez-Delgado, Franck Court, Enrique Vidal, et al.
Epigenomics|July 3, 2018
Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platformJose R Hernandez Mora, Chiharu Tayama, Marta Sánchez-Delgado, et al.
Journal of Medical Genetics|February 13, 2021
Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndromeJoan Sabria-Back, Ana Monteagudo-Sánchez, Marta Sánchez-Delgado, et al.
Clinical Epigenetics|February 28, 2019
Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restrictionAna Monteagudo-Sánchez, Marta Sánchez-Delgado, Jose Ramon Hernandez Mora, et al.
Pageof 11

Showing results (71-80 of 101) with videos related to

Sort By:
Pageof 11
Nucleic Acids Research|February 9, 2011
Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genesDavid Monk, Philippe Arnaud, Jennifer M Frost, et al.
Human Mutation|March 4, 2017
Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprintedMiguel Alsina Casanova, Ana Monteagudo-Sánchez, Luciana Rodiguez Guerineau, et al.
Neurology|June 19, 2016
Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 familiesAnne S Soehn, Tim W Rattay, Stefanie Beck-Wödl, et al.
Nucleic Acids Research|October 14, 2020
The role of ZFP57 and additional KRAB-zinc finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbancesAna Monteagudo-Sánchez, Jose Ramon Hernandez Mora, Carlos Simon, et al.
Epigenetics|June 26, 2025
<i>PIK3R1</i> and <i>G0S2</i> are human placenta-specific imprinted genes associated with germline-inherited maternal DNA methylationDagne Daskeviciute, Becky Sainty, Louise Chappell-Maor, et al.
Nature Medicine|May 9, 2018
PM20D1 is a quantitative trait locus associated with Alzheimer's diseaseJose V Sanchez-Mut, Holger Heyn, Bianca A Silva, et al.
Plos Genetics|November 12, 2016
Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient ImprintingMarta Sanchez-Delgado, Franck Court, Enrique Vidal, et al.
Epigenomics|July 3, 2018
Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platformJose R Hernandez Mora, Chiharu Tayama, Marta Sánchez-Delgado, et al.
Journal of Medical Genetics|February 13, 2021
Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndromeJoan Sabria-Back, Ana Monteagudo-Sánchez, Marta Sánchez-Delgado, et al.
Clinical Epigenetics|February 28, 2019
Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restrictionAna Monteagudo-Sánchez, Marta Sánchez-Delgado, Jose Ramon Hernandez Mora, et al.
Pageof 11