Literature DB >> 8032205

Parental imprinting of autosomal mammalian genes.

A Efstratiadis1.   

Abstract

The molecular mechanisms introducing epigenetic modifications that lead to differential silencing of some autosomal alleles depending on their parental legacy are still largely unknown, but recent results from studies of endogenously imprinted genes and particular transgenes make DNA methylation a strong candidate. At the same time, these results have raised new questions about the details of the imprinting process.

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Year:  1994        PMID: 8032205     DOI: 10.1016/s0959-437x(05)80054-1

Source DB:  PubMed          Journal:  Curr Opin Genet Dev        ISSN: 0959-437X            Impact factor:   5.578


  43 in total

1.  H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19.

Authors:  M Srivastava; S Hsieh; A Grinberg; L Williams-Simons; S P Huang; K Pfeifer
Journal:  Genes Dev       Date:  2000-05-15       Impact factor: 11.361

2.  Genetic conflicts in genomic imprinting.

Authors:  A Burt; R Trivers
Journal:  Proc Biol Sci       Date:  1998-12-22       Impact factor: 5.349

3.  The causes of synonymous rate variation in the rodent genome. Can substitution rates be used to estimate the sex bias in mutation rate?

Authors:  N G Smith; L D Hurst
Journal:  Genetics       Date:  1999-06       Impact factor: 4.562

4.  Phenotypic variation in a genetically identical population of mice.

Authors:  K Weichman; J R Chaillet
Journal:  Mol Cell Biol       Date:  1997-09       Impact factor: 4.272

5.  Genomic imprinting controls matrix attachment regions in the Igf2 gene.

Authors:  Michaël Weber; Hélène Hagège; Adele Murrell; Claude Brunel; Wolf Reik; Guy Cathala; Thierry Forné
Journal:  Mol Cell Biol       Date:  2003-12       Impact factor: 4.272

6.  Asynchronous replication timing of telomeres at opposite arms of mammalian chromosomes.

Authors:  Ying Zou; Sergei M Gryaznov; Jerry W Shay; Woodring E Wright; Michael N Cornforth
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-20       Impact factor: 11.205

Review 7.  Epigenetics and developmental programming of adult onset diseases.

Authors:  Lee O'Sullivan; Alexander N Combes; Karen M Moritz
Journal:  Pediatr Nephrol       Date:  2012-12       Impact factor: 3.714

8.  Gtl2lacZ, an insertional mutation on mouse chromosome 12 with parental origin-dependent phenotype.

Authors:  K Schuster-Gossler; D Simon-Chazottes; J L Guenet; J Zachgo; A Gossler
Journal:  Mamm Genome       Date:  1996-01       Impact factor: 2.957

9.  No evidence for uniparental disomy as a common cause of Sotos syndrome.

Authors:  M Smith; P Fullwood; Y Qi; S Palmer; M Upadhyaya; T Cole
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

10.  MBD-seq as a cost-effective approach for methylome-wide association studies: demonstration in 1500 case--control samples.

Authors:  Karolina A Aberg; Joseph L McClay; Srilaxmi Nerella; Lin Y Xie; Shaunna L Clark; Alexandra D Hudson; Jozsef Bukszár; Daniel Adkins; Christina M Hultman; Patrick F Sullivan; Patrik K E Magnusson; Edwin J C G van den Oord
Journal:  Epigenomics       Date:  2012-12       Impact factor: 4.778

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