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David Monk

Showing results (81-90 of 101) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|February 4, 2017
Human Amniocytes Are Receptive to Chemically Induced Reprogramming to PluripotencyKate E Hawkins, Dafni Moschidou, Danilo Faccenda, et al.
Elife|February 21, 2022
Environmentally sensitive hotspots in the methylome of the early human embryoMatt J Silver, Ayden Saffari, Noah J Kessler, et al.
Clinical Epigenetics|March 17, 2022
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequencesThomas Eggermann, Elzem Yapici, Jet Bliek, et al.
Epigenomics|June 21, 2016
Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbancesSusanne Bens, Julia Kolarova, Jasmin Beygo, et al.
Genome Research|January 10, 2014
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishmentFranck Court, Chiharu Tayama, Valeria Romanelli, et al.
Journal of Medical Genetics|November 25, 2010
Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanismValeria Romanelli, Julián Nevado, Mario Fraga, et al.
European Journal of Human Genetics : EJHG|May 12, 2016
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndromeKatja Eggermann, Jet Bliek, Frédéric Brioude, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniquesJair Tenorio, Valeria Romanelli, Alex Martin-Trujillo, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|January 21, 2015
The role and interaction of imprinted genes in human fetal growthGudrun E Moore, Miho Ishida, Charalambos Demetriou, et al.
Clinical Epigenetics|April 26, 2026
Investigation of multilocus imprinting disturbance (MLID) in 101 Beckwith-Wiedemann spectrum patientsMario Cazalla, Alejandro Parra, Carlos Rodríguez-Antolín, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 4, 2017
Human Amniocytes Are Receptive to Chemically Induced Reprogramming to PluripotencyKate E Hawkins, Dafni Moschidou, Danilo Faccenda, et al.
Elife|February 21, 2022
Environmentally sensitive hotspots in the methylome of the early human embryoMatt J Silver, Ayden Saffari, Noah J Kessler, et al.
Clinical Epigenetics|March 17, 2022
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequencesThomas Eggermann, Elzem Yapici, Jet Bliek, et al.
Epigenomics|June 21, 2016
Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbancesSusanne Bens, Julia Kolarova, Jasmin Beygo, et al.
Genome Research|January 10, 2014
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishmentFranck Court, Chiharu Tayama, Valeria Romanelli, et al.
Journal of Medical Genetics|November 25, 2010
Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanismValeria Romanelli, Julián Nevado, Mario Fraga, et al.
European Journal of Human Genetics : EJHG|May 12, 2016
EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndromeKatja Eggermann, Jet Bliek, Frédéric Brioude, et al.
American Journal of Medical Genetics. Part A|August 3, 2016
Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniquesJair Tenorio, Valeria Romanelli, Alex Martin-Trujillo, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|January 21, 2015
The role and interaction of imprinted genes in human fetal growthGudrun E Moore, Miho Ishida, Charalambos Demetriou, et al.
Clinical Epigenetics|April 26, 2026
Investigation of multilocus imprinting disturbance (MLID) in 101 Beckwith-Wiedemann spectrum patientsMario Cazalla, Alejandro Parra, Carlos Rodríguez-Antolín, et al.
Pageof 11