Time to take epigenetic inheritance seriously (Q78439222)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12404095%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

title

Time to take epigenetic inheritance seriously (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12404095%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

author name string

Marcus E Pembrey

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12404095%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

publication date

1 November 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12404095%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

14 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12404095%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12404095%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12404095%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

page(s)

669-671

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12404095%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200901

14 December 2019

exact match

0 references

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7 January 2021

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BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma

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7 January 2021

The novel BORIS + CTCF gene family is uniquely involved in the epigenetics of normal biology and cancer

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CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease

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