Literature DB >> 2692240

Genomic imprinting and genetic disorders in man.

W Reik.   

Abstract

In a considerable number of genetic disorders in the human, the phenotypic expression of the disease can depend on maternal or paternal inheritance of the mutation. It is suggested that genomic imprinting, an epigenetic process that marks maternal and paternal chromosomes in mammals, is involved in such parental effects.

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Year:  1989        PMID： 2692240     DOI： 10.1016/0168-9525(89)90138-8

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


  36 in total

Review 1.  Chromosome imbalance, normal phenotype, and imprinting.

Authors:  L Bortotto; E Piovan; R Furlan; H Rivera; O Zuffardi
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

2.  Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.

Authors:  H G Harley; K V Walsh; S Rundle; J D Brook; M Sarfarazi; M C Koch; J L Floyd; P S Harper; D J Shaw
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

3.  Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.

Authors:  R Tupler; L Bortotto; E M Bühler; M Alkan; N J Malik; N Bösch-Al Jadooa; L Memo; P Maraschio
Journal:  J Med Genet       Date:  1992-01       Impact factor: 6.318

4.  Triploidy after in vitro fertilization: cytogenetic analysis of human zygotes and embryos.

Authors:  M H Pieters; J C Dumoulin; R C Ignoul-Vanvuchelen; M Bras; J L Evers; J P Geraedts
Journal:  J Assist Reprod Genet       Date:  1992-02       Impact factor: 3.412

5.  2005 Curt Stern Award address. Exploring along a crooked path.

Authors:  Patrick O Brown
Journal:  Am J Hum Genet       Date:  2006-09       Impact factor: 11.025

Review 6.  Biological aspects of cytosine methylation in eukaryotic cells.

Authors:  M Hergersberg
Journal:  Experientia       Date:  1991-12-01

Review 7.  Chromosomal changes: radiation sensitive sites on chromosome 2 and their role in radiation myeloid leukaemogenesis in the mouse.

Authors:  R Cox; G Breckon; A R Silver; W K Masson; A M George
Journal:  Radiat Environ Biophys       Date:  1991       Impact factor: 1.925

8.  Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome.

Authors:  O W Quarrell; R G Snell; M A Curtis; S H Roberts; P S Harper; D J Shaw
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

9.  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

10.  Gametic imprinting effects on rate and composition of pig growth.

Authors:  A G de Vries; R Kerr; B Tier; T Long; T H Meuwissen
Journal:  Theor Appl Genet       Date:  1994-09       Impact factor: 5.699
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