Methylation status of genes flanking the fragile site in males with the fragile-X syndrome: a test of the imprinting hypothesis (Q35197941)

7 August 2017

title

Methylation status of genes flanking the fragile site in males with the fragile-X syndrome: a test of the imprinting hypothesis (English)

1 reference

7 August 2017

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M M Khalifa

1

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7 August 2017

A L Reiss

series ordinal

2

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7 August 2017

B R Migeon

series ordinal

3

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7 August 2017

language of work or name

English

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publication date

1 April 1990

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

46

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7 August 2017

issue

4

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7 August 2017

page(s)

744-753

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Fragile X syndrome: search for phenotypic manifestations at loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase

7 August 2017

cites work

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Completion of mouse embryogenesis requires both the maternal and paternal genomes

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Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation

13 July 2018

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Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3' CpG clusters: implications for X chromosome dosage compensation

13 July 2018

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"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

13 July 2018

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Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter

13 July 2018

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Specific methylation pattern at the 3′ end of the human housekeeping gene for glucose 6-phosphate dehydrogenase

13 July 2018

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A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

13 July 2018

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Differential activity of maternally and paternally derived chromosome regions in mice

13 July 2018

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Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome.

13 July 2018

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Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).

13 July 2018

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Psychiatric disability associated with the fragile X chromosome

13 July 2018

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Further segregation analysis of the fragile X syndrome with special reference to transmitting males

13 July 2018

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Autosomal suppressor gene for fragile-X: an hypothesis

13 July 2018

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Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

13 July 2018

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Phenotypic variation in male-transmitted fragile X: genetic inferences.

13 July 2018

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Fragile X syndrome: a unique mutation in man.

13 July 2018

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DNA methylation stabilizes X chromosome inactivation in eutherians but not in marsupials: evidence for multistep maintenance of mammalian X dosage compensation

13 July 2018

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Complete reactivation of X chromosomes from human chorionic villi with a switch to early DNA replication

13 July 2018

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

13 July 2018

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A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A.

13 July 2018

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Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

13 July 2018

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The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

13 July 2018

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Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA

13 July 2018

1 reference

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Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clusters

13 July 2018

1 reference

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The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683650

Toward a physical map of the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683650

The marker (X) syndrome: a cytogenetic and genetic analysis.

13 July 2018

1 reference

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Genomic imprinting determines methylation of parental alleles in transgenic mice

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683650

An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767).

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683650

Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome

26 September 2018

1 reference

12 December 2020

Degree of methylation of transgenes is dependent on gamete of origin

1 reference

12 December 2020

Parental legacy determines methylation and expression of an autosomal transgene: a molecular mechanism for parental imprinting

1 reference

12 December 2020

Parental origin effects in mice

1 reference

12 December 2020

Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation.

1 reference

12 December 2020

Transmission of fragile (X) (q27) site from a male

1 reference

12 December 2020

Identifiers

PMC publication ID

1683650

1 reference

7 August 2017

1 reference