Genomic Imprinting Disrupted by a Maternal Effect Mutation in the Dnmt1 Gene-Reference-Cited by-同舟云学术

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Genomic Imprinting Disrupted by a Maternal Effect Mutation in the Dnmt1 Gene

Published:2001-03 Issue:6 Volume:104 Page:829-838
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Howell Carina Y.,Bestor Timothy H.,Ding Feng,Latham Keith E.,Mertineit Carmen,Trasler Jacquetta M.,Chaillet J.Richard

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference49 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

2. Epigenetic modifications necessary for normal development are established during oocyte growth in mice;Bao;Biol. Reprod.,2000

3. Subcellular localization of annexin V in human foreskin fibroblasts;Barwise;FEBS Lett.,1996

4. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene;Bell;Nature,2000

5. The DNA methyltransferases of mammals;Bestor;Hum. Mol. Gen.,2000

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1. DNMT1 Y495C mutation interferes with maintenance methylation of imprinting control regions;The International Journal of Biochemistry & Cell Biology;2024-04

2. United by conflict: Convergent signatures of parental conflict in angiosperms and placental mammals;Journal of Heredity;2024-02-16

3. Human promoter CpG islands contain primate-specific repeats, cluster and resist reprogramming;2024-01-20

4. Dynamic methylation pattern of H19DMR and KvDMR1 in bovine oocytes and preimplantation embryos;Journal of Assisted Reproduction and Genetics;2024-01-17

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