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Literature DB >> 19147911

May anomalous X chromosome methylation be responsible for the spontaneous abortion of a male foetus?

R Martínez¹, V Bonilla-Henao, I Ramos, F Sobrino, M Lucas, E Pintado.

Abstract

Mesh：

Year: 2008 PMID： 19147911 DOI： 10.1007/s12041-008-0040-4

Source DB: PubMed Journal: J Genet ISSN： 0022-1333 Impact factor: 1.166

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20 in total

Review 1. X-chromosome inactivation: counting, choice and initiation.

Authors: P Avner; E Heard
Journal: Nat Rev Genet Date: 2001-01 Impact factor: 53.242

2. The region 3' to Xist mediates X chromosome counting and H3 Lys-4 dimethylation within the Xist gene.

Authors: Céline Morey; Pablo Navarro; Emmanuel Debrand; Philip Avner; Claire Rougeulle; Philippe Clerc
Journal: EMBO J Date: 2004-01-29 Impact factor: 11.598

Review 3. Delving into the diversity of facultative heterochromatin: the epigenetics of the inactive X chromosome.

Authors: Edith Heard
Journal: Curr Opin Genet Dev Date: 2005-10 Impact factor: 5.578

4. A simple salting out procedure for extracting DNA from human nucleated cells.

Authors: S A Miller; D D Dykes; H F Polesky
Journal: Nucleic Acids Res Date: 1988-02-11 Impact factor: 16.971

Review 5. Random X-chromosome inactivation: skewing lessons for mice and men.

Authors: Philippe Clerc; Philip Avner
Journal: Curr Opin Genet Dev Date: 2006-05-02 Impact factor: 5.578

6. Skewed X inactivation of the normal allele in fully mutated female carriers determines the levels of FMRP in blood and the fragile X phenotype.

Authors: Raquel Martínez; Victoria Bonilla-Henao; Antonio Jiménez; Miguel Lucas; Carmen Vega; Inmaculada Ramos; Francisco Sobrino; Elizabeth Pintado
Journal: Mol Diagn Date: 2005

May anomalous X chromosome methylation be responsible for the spontaneous abortion of a male foetus?

Review 1. X-chromosome inactivation: counting, choice and initiation.

2. The region 3' to Xist mediates X chromosome counting and H3 Lys-4 dimethylation within the Xist gene.

Review 3. Delving into the diversity of facultative heterochromatin: the epigenetics of the inactive X chromosome.

4. A simple salting out procedure for extracting DNA from human nucleated cells.

Review 5. Random X-chromosome inactivation: skewing lessons for mice and men.

6. Skewed X inactivation of the normal allele in fully mutated female carriers determines the levels of FMRP in blood and the fragile X phenotype.

Review 7. X chromosome defects as an etiology of recurrent spontaneous abortion.

8. Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.

9. Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females.

Review 10. Meiotic sex chromosome inactivation.