The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes (Q35246364)

14 November 2017

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title

The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes (English)

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14 November 2017

Lyon MF

1

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PMCID

1715299

14 November 2017

language of work or name

English

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publication date

1 January 1988

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American Journal of Human Genetics

14 November 2017

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14 November 2017

42

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14 November 2017

1

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14 November 2017

8-16

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Sex chromatin and gene action in the mammalian X-chromosome

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Differential expression of steroid sulphatase locus on active and inactive human X chromosome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Inactive X chromosome DNA does not function in DNA-mediated cell transformation for the hypoxanthine phosphoribosyltransferase gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Completion of mouse embryogenesis requires both the maternal and paternal genomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Methylation patterns of repetitive DNA sequences in germ cells of Mus musculus

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Comparative studies on X-autosome translocations in the mouse. II. Inactivation of autosomal loci, segregation, and mapping of autosomal breakpoints in five T (X;1) S.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Replication of X chromosomes in complete moles

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Glucose-6-phosphate dehydrogenase

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Incomplete X chromosome dosage compensation in chorionic villi of human placenta

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Polymorphism of the long-wavelength cone in normal human colour vision

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

The Gy mutation: another cause of X-linked hypophosphatemia in mouse

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Methylation of the mouse hprt gene differs on the active and inactive X chromosomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Detailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecific Mus spretus mouse cross

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Steroid sulfatase deficiency and the genetics of the short arm of the human X chromosome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Selective silencing of eukaryotic DNA

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

X inactivation, differentiation, and DNA methylation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Chromosome imprinting and the mammalian X chromosome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

The use of mouse X-autosome translocations in the study of X-inactivation pathways and nonrandomness

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

X-linked syndrome of congenital ichthyosis, hypogonadism, mental retardation and anosmia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Parental source of chromosome imprinting and its relevance for X chromosome inactivation.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715299

Differential expression of α-fetoprotein genes on the inactive X chromosome in extraembryonic and somatic tissues of a transgenic mouse line

26 September 2018

1 reference

12 December 2020

Preferential X-chromosome activity in human female placental tissues

1 reference

12 December 2020

X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome

1 reference

12 December 2020

Correlation between X-chromosome inactivation and cell differentiation in female preimplantation mouse embryos

1 reference

12 December 2020

Clonal analysis of X-chromosome inactivation and the origin of the germ line in the mouse embryo

1 reference

12 December 2020

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis

1 reference

12 December 2020

X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22

1 reference

12 December 2020

Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity

1 reference

12 December 2020

Perception. Questions of sex and colour

1 reference

12 December 2020

Methylation and the X chromosome

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12 December 2020

A linkage study of Emery-Dreifuss muscular dystrophy

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12 December 2020

Lack of inactivation of a mouse X-linked gene physically separated from the inactivation centre

1 reference

12 December 2020

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12 December 2020

Influence of germline modifications of homologous chromosomes on mouse development

1 reference

12 December 2020

Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development

1 reference

12 December 2020

Mammalian X-chromosome action: inactivation limited in spread and region of origin

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12 December 2020

Position effect variegation in the mouse

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12 December 2020

DNA modification mechanisms and gene activity during development

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12 December 2020

X–chromosome inactivation during differentiation of female teratocarcinoma stem cells in vitro

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12 December 2020

X chromosome inactivation in diploid parthenogenetic mouse embryos

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12 December 2020

Preferential inactivation of the paternally derived X chromosome in mice

1 reference

12 December 2020

Cell lineage-specific undermethylation of mouse repetitive DNA

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12 December 2020

Ichthyosis vulgaris with hypogenitalism and hypogonadism: evidence for different genotypes by lipoprotein electrophoresis and steroid sulfatase testing

1 reference

12 December 2020

Timing of X-chromosome inactivation in postimplantation mouse embryos

1 reference

12 December 2020

Homologous genes for X-linked chondrodysplasia punctata in man and mouse

1 reference

12 December 2020

Reversal of X-inactivation in female mouse somatic cells hybridized with murine teratocarcinoma stem cells in vitro

1 reference

12 December 2020

Mapping of the X-linked immune deficiency mutation (xid) of CBA/N mice

1 reference

12 December 2020

Sequential X chromosome inactivation coupled with cellular differentiation in early mouse embryos

1 reference

12 December 2020

X-chromosome inactivation in extra-embryonic membranes of diploid parthenogenetic mouse embryos demonstrated by differential staining

1 reference

12 December 2020

Relationship between the parental origin of the X chromosomes, embryonic cell lineage and X chromosome expression in mice

1 reference

12 December 2020

Differences in the DNA of the inactive X chromosomes of fetal and extraembryonic tissues of mice

1 reference

12 December 2020

Variations of colour vision in a New World primate can be explained by polymorphism of retinal photopigments

1 reference

12 December 2020

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1 reference

12 December 2020

Identifiers

PMCID

1715299

1 reference

14 November 2017

1 reference

PMCID

1715299