Analysis of H19 methylation in control and abnormal human embryos, sperm and oocytes

Russell–Silver syndrome due to paternal H19/IGF2 hypomethylation in a patient conceived using intracytoplasmic sperm injection

(2010) M. Chopra et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men

(2009) Céline Chalas Boissonnas et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

DNA methylation errors at imprinted loci after assisted conception originate in the parental sperm

(2009) Hisato Kobayashi et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner

(2009) Brenna A. Market-Velker et al.   HUMAN MOLECULAR GENETICS

Assisted Reproductive Technology, Epigenetics, and Long-Term Health: A Developmental Time Bomb Still Ticking

(2009) Kristen Grace et al.   SEMINARS IN REPRODUCTIVE MEDICINE

Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development

(2008) R. Hirasawa et al.   GENES & DEVELOPMENT

Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia

(2008) C.J. Marques et al.   MOLECULAR HUMAN REPRODUCTION

The H19 locus acts in vivo as a tumor suppressor

(2008) T. Yoshimizu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA