(Q52241634)

English

Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations

scientific article published on May 1, 1990

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/1694309

Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations (English)

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

dosage compensation

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1694309

31 October 2022

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

author name string

D. J. Driscoll

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1694309

31 October 2022

B. R. Migeon

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1694309

31 October 2022

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1694309

31 October 2022

publication date

1 May 1990

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/1694309

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF01233363.pdf

Portable Document Format

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

http://link.springer.com/article/10.1007/BF01233363/fulltext.html

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

http://link.springer.com/content/pdf/10.1007/BF01233363

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Somatic Cell and Molecular Genetics

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/1694309

16

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/1694309

3

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/1694309

267-282

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/1694309

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

1

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

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

2

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase

3

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

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

5

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Methylation of the Hprt gene on the inactive X occurs after chromosome inactivation

6

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Incomplete X chromosome dosage compensation in chorionic villi of human placenta

7

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Differential methylation of hypoxanthine phosphoribosyltransferase genes on active and inactive human X chromosomes

8

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

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

9

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Evidence for two functional X chromosomes in human oocytes

10

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Evidence for two active X chromosomes in germ cells of female before meiotic entry

11

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

X chromosome reactivation in oocytes of Mus caroli

12

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Forensic application of DNA ‘fingerprints’

13

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

OBSERVATIONS ON THE MOVEMENTS OF THE LIVING PRIMORDIAL GERM CELLS IN THE MOUSE

14

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Frequent derepression of G6PD and HPRT on the marsupial inactive X chromosome associated with cell proliferation in vitro

15

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

CpG islands of the X chromosome are gene associated

16

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Signal sequence and DNA-mediated expression of human lysosomal alpha-galactosidase A

17

1 reference

10.1007/BF01233363

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31 October 2022

Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3' untranslated region

18

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

The gene structure of human anti-haemophilic factor IX.

19

1 reference

10.1007/BF01233363

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31 October 2022

An Xba I polymorphism 3' to the human erythropoietin (EPO) gene

21

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Isolation and characterization of genomic and cDNA clones of human erythropoietin

22

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

A quantitative and cytological study of germ cells in human ovaries

23

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

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

24

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

A study of X chromosome regulation during oogenesis in the mouse

25

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse

26

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

The anatomy and histology of XO human embryos and fetuses

28

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Histology of the ovary

29

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

The normal ovary of childhood

30

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Quantification of human seminiferous epithelium. I. Histological studies in twenty-one fertile men with normal chromosome complements

31

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

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

32

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Human testis-specific PGK gene lacks introns and possesses characteristics of a processed gene

33

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Chromatin structure and de novo methylation of sperm DNA: implications for activation of the paternal genome

34

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

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

35

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Somatic and germ-cell sex in mammals

37

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Completion of mouse embryogenesis requires both the maternal and paternal genomes

38

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

39

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Differential activity of maternally and paternally derived chromosome regions in mice

40

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

41

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Inheritance of allelic blueprints for methylation patterns.

43

1 reference

10.1007/BF01233363

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31 October 2022

The CpG dinucleotide and human genetic disease

44

1 reference

10.1007/BF01233363

https://api.crossref.org/works/10.1007/BF01233363

31 October 2022

Identifiers

10.1007/BF01233363

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/1694309

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 April 2018

http://europepmc.org/abstract/MED/1694309

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