Literature DB >> 3076291

Transgenes as molecular probes for genomic imprinting.

M A Surani, W Reik, N D Allen.   

Abstract

Mesh：

Year:  1988        PMID： 3076291     DOI： 10.1016/0168-9525(88)90040-6

Source DB:  PubMed          Journal:  Trends Genet        ISSN： 0168-9525            Impact factor:   11.639


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  23 in total

1.  Epigenetic asymmetry in the mammalian zygote and early embryo: relationship to lineage commitment?

Authors:  Wolf Reik; Fatima Santos; Kohzoh Mitsuya; Hugh Morgan; Wendy Dean
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2003-08-29       Impact factor: 6.237

Review 2.  Genomic imprinting.

Authors:  J G Hall
Journal:  Arch Dis Child       Date:  1990-10       Impact factor: 3.791

3.  Investigation of elements sufficient to imprint the mouse Air promoter.

Authors:  F Sleutels; D P Barlow
Journal:  Mol Cell Biol       Date:  2001-08       Impact factor: 4.272

4.  Two-dimensional electrophoretic protein patterns of reciprocal hybrids of the mouse strains DBA and C57BL.

Authors:  T Vogel; J Klose
Journal:  Biochem Genet       Date:  1992-12       Impact factor: 1.890

Review 5.  Confined placental mosaicism.

Authors:  D K Kalousek; M Vekemans
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

Review 6.  Genomic imprinting: review and relevance to human diseases.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

7.  DNA methylation patterns associated with asparagine synthetase expression in asparagine-overproducing and -auxotrophic cells.

Authors:  I L Andrulis; M T Barrett
Journal:  Mol Cell Biol       Date:  1989-07       Impact factor: 4.272

8.  Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?

Authors:  R Voss; E Ben-Simon; A Avital; S Godfrey; J Zlotogora; J Dagan; Y Tikochinski; J Hillel
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

9.  Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome.

Authors:  H Schneid; D Seurin; M P Vazquez; M Gourmelen; S Cabrol; Y Le Bouc
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

10.  Uniparental disomy for chromosome 16 in humans.

Authors:  D K Kalousek; S Langlois; I Barrett; I Yam; D R Wilson; P N Howard-Peebles; M P Johnson; E Giorgiutti
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025
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