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David Monk

Showing results (61-70 of 101) with videos related to

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Clinical Epigenetics|November 20, 2015
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.
Genome Medicine|December 19, 2019
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisationHannah Demond, Zahra Anvar, Bahia Namavar Jahromi, et al.
Scientific Reports|February 1, 2019
Wnt/β-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cellsIlda Theka, Francesco Sottile, Marco Cammisa, et al.
Plos Genetics|November 7, 2015
Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific ImprintingMarta Sanchez-Delgado, Alejandro Martin-Trujillo, Chiharu Tayama, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|November 30, 2025
Single operator learning curve and insights into the adoption of transoral incisionless fundoplication 2.0 in the UKBenjamin Norton, Nasar Aslam, Apostolis Papaefthymiou, et al.
American Journal of Human Genetics|March 27, 2012
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightMiho Ishida, David Monk, Andrew J Duncan, et al.
Clinical Epigenetics|January 29, 2016
Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defectsAnne Rochtus, Alejandro Martin-Trujillo, Benedetta Izzi, et al.
Journal of Hematology & Oncology|January 11, 2014
Hypermethylation of the alternative AWT1 promoter in hematological malignancies is a highly specific marker for acute myeloid leukemias despite high expression levelsAmy Guillaumet-Adkins, Julia Richter, Maria D Odero, et al.
Nature Reviews. Disease Primers|June 29, 2023
Imprinting disordersThomas Eggermann, David Monk, Guiomar Perez de Nanclares, et al.
Cell Reports|February 10, 2023
Single-cell multi-omic analysis profiles defective genome activation and epigenetic reprogramming associated with human pre-implantation embryo arrestJose Ramon Hernandez Mora, Claudia Buhigas, Stephen Clark, et al.
Pageof 11

Showing results (61-70 of 101) with videos related to

Sort By:
Pageof 11
Clinical Epigenetics|November 20, 2015
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.
Genome Medicine|December 19, 2019
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisationHannah Demond, Zahra Anvar, Bahia Namavar Jahromi, et al.
Scientific Reports|February 1, 2019
Wnt/β-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cellsIlda Theka, Francesco Sottile, Marco Cammisa, et al.
Plos Genetics|November 7, 2015
Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific ImprintingMarta Sanchez-Delgado, Alejandro Martin-Trujillo, Chiharu Tayama, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|November 30, 2025
Single operator learning curve and insights into the adoption of transoral incisionless fundoplication 2.0 in the UKBenjamin Norton, Nasar Aslam, Apostolis Papaefthymiou, et al.
American Journal of Human Genetics|March 27, 2012
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightMiho Ishida, David Monk, Andrew J Duncan, et al.
Clinical Epigenetics|January 29, 2016
Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defectsAnne Rochtus, Alejandro Martin-Trujillo, Benedetta Izzi, et al.
Journal of Hematology & Oncology|January 11, 2014
Hypermethylation of the alternative AWT1 promoter in hematological malignancies is a highly specific marker for acute myeloid leukemias despite high expression levelsAmy Guillaumet-Adkins, Julia Richter, Maria D Odero, et al.
Nature Reviews. Disease Primers|June 29, 2023
Imprinting disordersThomas Eggermann, David Monk, Guiomar Perez de Nanclares, et al.
Cell Reports|February 10, 2023
Single-cell multi-omic analysis profiles defective genome activation and epigenetic reprogramming associated with human pre-implantation embryo arrestJose Ramon Hernandez Mora, Claudia Buhigas, Stephen Clark, et al.
Pageof 11