(Q45133324)

English

Hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural fold elevation

scientific article published on 2 July 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

Hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural fold elevation (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

author name string

Diana M Juriloff

1

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

Muriel J Harris

2

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

publication date

2 July 2012

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

Birth Defects Research Part A: Clinical and Molecular Teratology

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

94

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

849-855

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

High-frequency developmental abnormalities in p53-deficient mice.

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SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation

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Neurofibromin binds to caveolin-1 and regulates ras, FAK, and Akt

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Female predisposition to cranial neural tube defects is not because of a difference between the sexes in the rate of embryonic growth or development during neurulation.

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The prevalence and predictors of anencephaly and spina bifida in Texas

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X-inactivation profile reveals extensive variability in X-linked gene expression in females

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Crooked tail (Cd) models human folate-responsive neural tube defects

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Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control study

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Sex difference in neural tube defects in p53-null mice is caused by differences in the complement of X not Y genes

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The impact of retrotransposons on human genome evolution

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Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects

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Retrotransposon-derived elements in the mammalian genome: a potential source of disease

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Expression of a new mutation (Axd) causing axial defects in mice correlates with maternal phenotype and age.

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Insights into prevention of human neural tube defects by folic acid arising from consideration of mouse mutants

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Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects

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An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure

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21 January 2018

MARCKS is an actin filament crosslinking protein regulated by protein kinase C and calcium-calmodulin

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21 January 2018

Transcriptional analysis of Gli3 mutants identifies Wnt target genes in the developing hippocampus

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Regulation of repulsion versus adhesion by different splice forms of an Eph receptor

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Overlapping roles for homeodomain-interacting protein kinases hipk1 and hipk2 in the mediation of cell growth in response to morphogenetic and genotoxic signals

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Mouse models for neural tube closure defects

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21 January 2018

Genomic DNA methylation: the mark and its mediators

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Neurofibromin deficiency in mice causes exencephaly and is a modifier for Splotch neural tube defects

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21 January 2018

Sex differences in the prevalence of human birth defects: a population-based study

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Extremely high prevalence of neural tube defects in a 4-county area in Shanxi Province, China.

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Sex and congenital malformations: an international perspective.

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Developmental study of neural tube closure in a mouse stock with a high incidence of exencephaly.

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Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

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DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

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The DNA sequence of the human X chromosome

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Differential risks to males and females for congenital malformations among 2.5 million California births, 1989-1997.

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The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

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MARCKS deficiency in mice leads to abnormal brain development and perinatal death

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Sex differences in the prevalence of congenital anomalies: a population-based study

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Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects

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Sexual dimorphism in mammalian autosomal gene regulation is determined not only by Sry but by sex chromosome complement as well.

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Folic acid supplementation for the prevention of neural tube defects: an update of the evidence for the U.S. Preventive Services Task Force

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NEURAL TUBE DEFECTS, SEX RATIOS, AND X INACTIVATTON

1 reference

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21 January 2018

Identifiers

10.1002/BDRA.23036

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

release_miqhhrk2orbibdgqhfnu77sc3m

1 reference

https://api.fatcat.wiki/v0/release/miqhhrk2orbibdgqhfnu77sc3m

24 November 2022

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

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