Literature DB >> 9735381

A catalogue of imprinted genes and parent-of-origin effects in humans and animals.

I M Morison1, A E Reeve.   

Abstract

Parent-of-origin effects were first recorded >3000 years ago by mule breeders in Asia Minor. There are now several different types of evidence suggesting the presence of a large number of imprinted genes, many of which have not yet been identified. Here, we catalogue a wide range of evidence and phenomena which indicate or suggest the presence of genomic imprinting in animals. This evidence includes: the direct documentation of parent-of-origin-specific gene transcription; human disease inheritance patterns which suggest the involvement of imprinted genes; and older, less well studied animal models which may show parent-of-origin effects.

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Year:  1998        PMID: 9735381     DOI: 10.1093/hmg/7.10.1599

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  54 in total

1.  Bivalent 15 regularly associates with the sex vesicle in normal male meiosis.

Authors:  C Metzler-Guillemain; C Mignon; D Depetris; M R Guichaoua; M G Mattei
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

2.  The imprinted gene and parent-of-origin effect database.

Authors:  I M Morison; C J Paton; S D Cleverley
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

Review 3.  The impact of genomic imprinting for neurobehavioral and developmental disorders.

Authors:  R D Nicholls
Journal:  J Clin Invest       Date:  2000-02       Impact factor: 14.808

Review 4.  Genomic imprinting: implications for human disease.

Authors:  J G Falls; D J Pulford; A A Wylie; R L Jirtle
Journal:  Am J Pathol       Date:  1999-03       Impact factor: 4.307

5.  Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation.

Authors:  A A Wylie; S K Murphy; T C Orton; R L Jirtle
Journal:  Genome Res       Date:  2000-11       Impact factor: 9.043

Review 6.  Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.

Authors:  M P Hitchins; P Stanier; M A Preece; G E Moore
Journal:  J Med Genet       Date:  2001-12       Impact factor: 6.318

Review 7.  Mechanisms of genomic imprinting.

Authors:  K Pfeifer
Journal:  Am J Hum Genet       Date:  2000-09-05       Impact factor: 11.025

Review 8.  The genetics of the Silver-Russell syndrome.

Authors:  Michael A Preece
Journal:  Rev Endocr Metab Disord       Date:  2002-12       Impact factor: 6.514

9.  A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q.

Authors:  Yoichi Yamada; Hidemi Watanabe; Fumihito Miura; Hidenobu Soejima; Michiko Uchiyama; Tsuyoshi Iwasaka; Tsunehiro Mukai; Yoshiyuki Sakaki; Takashi Ito
Journal:  Genome Res       Date:  2004-02       Impact factor: 9.043

10.  Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion.

Authors:  Sami Tsukishiro; Qing Ying Li; Mitsuyo Tanemura; Mayumi Sugiura-Ogasawara; Kaoru Suzumori; Shin-Ichi Sonta
Journal:  J Hum Genet       Date:  2005-03-04       Impact factor: 3.172

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