Literature DB >> 12402273

Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation.

Esther M Maier1, Stefan Kammerer, Ania C Muntau, Maria Wichers, Andreas Braun, Adelbert A Roscher.   

Abstract

Skewing of X inactivation may contribute to the manifestation of symptoms in adrenoleukodystrophy carriers. We observed highly skewed X inactivation in 32% of 22 symptomatic and asymptomatic carriers but not in 7 related and 35 unrelated controls. Skewing of X inactivation correlated with clinical neurological scores but not with the extent of very long-chain fatty acid accumulation. Transcript analysis in cultured fibroblasts revealed that skewing could occur both in favor of the mutant and the wild-type allele. Adrenoleukodystrophy carriers are more susceptible to develop skewing of X inactivation in favor of the mutant allele being associated with the manifestation of symptoms.

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Year:  2002        PMID: 12402273     DOI: 10.1002/ana.10376

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  29 in total

1.  IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features.

Authors:  Erin L Youngs; Rebecca Henkhaus; Jessica A Hellings; Merlin G Butler
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Review 2.  X chromosome inactivation in clinical practice.

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3.  Levodopa response reveals sepiapterin reductase deficiency in a female heterozygote with adrenoleukodystrophy.

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4.  X chromosome inactivation in women with alcoholism.

Authors:  Ann M Manzardo; Rebecca Henkhaus; Brandon Hidaka; Elizabeth C Penick; Albert B Poje; Merlin G Butler
Journal:  Alcohol Clin Exp Res       Date:  2012-02-29       Impact factor: 3.455

5.  X-chromosome inactivation patterns in females with Prader-Willi syndrome.

Authors:  Merlin G Butler; Mariana F Theodoro; Douglas C Bittel; Paul J Kuipers; Daniel J Driscoll; Zohreh Talebizadeh
Journal:  Am J Med Genet A       Date:  2007-03-01       Impact factor: 2.802

6.  Brief report: non-random X chromosome inactivation in females with autism.

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Journal:  J Autism Dev Disord       Date:  2005-10

7.  Comparison of X-chromosome inactivation patterns in multiple tissues from human females.

Authors:  D C Bittel; M F Theodoro; N Kibiryeva; W Fischer; Z Talebizadeh; M G Butler
Journal:  J Med Genet       Date:  2007-12-21       Impact factor: 6.318

Review 8.  Expression of the disease on female carriers of X-linked lysosomal disorders: a brief review.

Authors:  Louise L C Pinto; Taiane A Vieira; Roberto Giugliani; Ida V D Schwartz
Journal:  Orphanet J Rare Dis       Date:  2010-05-28       Impact factor: 4.123

9.  Is gestation in Prader-Willi syndrome affected by the genetic subtype?

Authors:  Merlin G Butler; Jennifer Sturich; Susan E Myers; June-Anne Gold; Virginia Kimonis; Daniel J Driscoll
Journal:  J Assist Reprod Genet       Date:  2009-09-17       Impact factor: 3.412

Review 10.  Dominant versus recessive: molecular mechanisms in metabolic disease.

Authors:  Johannes Zschocke
Journal:  J Inherit Metab Dis       Date:  2008-10-21       Impact factor: 4.982

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