Literature DB >> 8841173

Imprinting moves to the centre.

A C Ferguson-Smith.   

Abstract

Mesh:

Year:  1996        PMID: 8841173     DOI: 10.1038/ng1096-119

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


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  4 in total

1.  Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila.

Authors:  F Lyko; K Buiting; B Horsthemke; R Paro
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

2.  Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

Authors:  J Bürger; K Buiting; B Dittrich; S Gross; C Lich; K Sperling; B Horsthemke; A Reis
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

3.  Chromatin assembly factor I contributes to the maintenance, but not the re-establishment, of silencing at the yeast silent mating loci.

Authors:  S Enomoto; J Berman
Journal:  Genes Dev       Date:  1998-01-15       Impact factor: 11.361

4.  Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.

Authors:  K Buiting; B Dittrich; S Gross; C Lich; C Färber; T Buchholz; E Smith; A Reis; J Bürger; M M Nöthen; U Barth-Witte; B Janssen; D Abeliovich; I Lerer; A M van den Ouweland; D J Halley; C Schrander-Stumpel; H Smeets; P Meinecke; S Malcolm; A Gardner; M Lalande; R D Nicholls; K Friend; A Schulze; G Matthijs; H Kokkonen; P Hilbert; L Van Maldergem; G Glover; P Carbonell; P Willems; G Gillessen-Kaesbach; B Horsthemke
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

  4 in total

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