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David Monk

Showing results (51-60 of 101) with videos related to

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Clinical Epigenetics|May 7, 2024
Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndromeNeus Baena, David Monk, Cinthia Aguilera, et al.
Biotechnology Progress|May 4, 2011
Passive multivariable temperature and conductivity RFID sensors for single-use biopharmaceutical manufacturing componentsRadislav A Potyrailo, Timothy Wortley, Cheryl Surman, et al.
Human Molecular Genetics|April 18, 2003
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same markPhilippe Arnaud, David Monk, Megan Hitchins, et al.
BMC Cancer|July 31, 2019
A case of intraplacental gestational choriocarcinoma; characterised by the methylation pattern of the early placenta and an absence of driver mutationsPhilip Savage, David Monk, Jose R Hernandez Mora, et al.
Annals of Surgical Oncology|March 14, 2024
Is Robotic Surgery the Future for Resectable Esophageal Cancer?: A Systematic Literature Review of Oncological and Clinical OutcomesNikhil Manish Patel, Pranav Harshad Patel, Kai Tai Derek Yeung, et al.
Plos One|June 23, 2012
Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatinIsabel Iglesias-Platas, Alex Martin-Trujillo, Davide Cirillo, et al.
Nature Genetics|February 28, 2007
STOX1 is not imprinted and is not likely to be involved in preeclampsiaIsabel Iglesias-Platas, David Monk, Jiska Jebbink, et al.
Human Molecular Genetics|May 20, 2011
Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genesKazuhiko Nakabayashi, Alex Martin Trujillo, Chiharu Tayama, et al.
Epigenetics & Chromatin|March 27, 2014
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locusFranck Court, Cristina Camprubi, Cristina Vicente Garcia, et al.
Clinical Epigenetics|March 10, 2016
Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted lociThomas Eggermann, Guiomar Perez de Nanclares, Eamonn R Maher, et al.
Pageof 11

Showing results (51-60 of 101) with videos related to

Sort By:
Pageof 11
Clinical Epigenetics|May 7, 2024
Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndromeNeus Baena, David Monk, Cinthia Aguilera, et al.
Biotechnology Progress|May 4, 2011
Passive multivariable temperature and conductivity RFID sensors for single-use biopharmaceutical manufacturing componentsRadislav A Potyrailo, Timothy Wortley, Cheryl Surman, et al.
Human Molecular Genetics|April 18, 2003
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same markPhilippe Arnaud, David Monk, Megan Hitchins, et al.
BMC Cancer|July 31, 2019
A case of intraplacental gestational choriocarcinoma; characterised by the methylation pattern of the early placenta and an absence of driver mutationsPhilip Savage, David Monk, Jose R Hernandez Mora, et al.
Annals of Surgical Oncology|March 14, 2024
Is Robotic Surgery the Future for Resectable Esophageal Cancer?: A Systematic Literature Review of Oncological and Clinical OutcomesNikhil Manish Patel, Pranav Harshad Patel, Kai Tai Derek Yeung, et al.
Plos One|June 23, 2012
Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatinIsabel Iglesias-Platas, Alex Martin-Trujillo, Davide Cirillo, et al.
Nature Genetics|February 28, 2007
STOX1 is not imprinted and is not likely to be involved in preeclampsiaIsabel Iglesias-Platas, David Monk, Jiska Jebbink, et al.
Human Molecular Genetics|May 20, 2011
Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genesKazuhiko Nakabayashi, Alex Martin Trujillo, Chiharu Tayama, et al.
Epigenetics & Chromatin|March 27, 2014
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locusFranck Court, Cristina Camprubi, Cristina Vicente Garcia, et al.
Clinical Epigenetics|March 10, 2016
Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted lociThomas Eggermann, Guiomar Perez de Nanclares, Eamonn R Maher, et al.
Pageof 11