Literature DB >> 2894755

Frequent alterations of visual pigment genes in adrenoleukodystrophy.

P R Aubourg1, G H Sack, H W Moser.   

Abstract

Both adrenoleukodystrophy (ALD) and red/green color blindness have been mapped to the distal long arm of the human X chromosome (Xq28). Color-vision defects are frequently associated with ALD, and study of the red and green visual pigment genes in eight ALD kindreds has shown frequent structural changes including deletions and possible intragenic recombinations. Such changes may reflect chromosomal events underlying both ALD and the associated visual defects and should help define both the structural gene responsible for ALD and physical genetic relationships in the Xq28 region.

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Year:  1988        PMID: 2894755      PMCID: PMC1715151     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  16 in total

1.  Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes.

Authors:  I H PORTER; J SCHULZE; V A MCKUSICK
Journal:  Ann Hum Genet       Date:  1962-11       Impact factor: 1.670

2.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

3.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

4.  Molecular genetics of inherited variation in human color vision.

Authors:  J Nathans; T P Piantanida; R L Eddy; T B Shows; D S Hogness
Journal:  Science       Date:  1986-04-11       Impact factor: 47.728

5.  Amplification and characterization of a beta-globin gene synthesized in vitro.

Authors:  T Maniatis; S G Kee; A Efstratiadis; F C Kafatos
Journal:  Cell       Date:  1976-06       Impact factor: 41.582

6.  Characterization of five partial deletions of the factor VIII gene.

Authors:  H Youssoufian; S E Antonarakis; S Aronis; G Tsiftis; D G Phillips; H H Kazazian
Journal:  Proc Natl Acad Sci U S A       Date:  1987-06       Impact factor: 11.205

7.  Assignment of the gene for dyskeratosis congenita to Xq28.

Authors:  J M Connor; D Gatherer; F C Gray; L A Pirrit; N A Affara
Journal:  Hum Genet       Date:  1986-04       Impact factor: 4.132

8.  Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.

Authors:  B R Migeon; H W Moser; A B Moser; J Axelman; D Sillence; R A Norum
Journal:  Proc Natl Acad Sci U S A       Date:  1981-08       Impact factor: 11.205

9.  Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.

Authors:  J Nathans; D Thomas; D S Hogness
Journal:  Science       Date:  1986-04-11       Impact factor: 47.728

10.  Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy.

Authors:  H W Moser; A E Moser; I Singh; B P O'Neill
Journal:  Ann Neurol       Date:  1984-12       Impact factor: 10.422

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  14 in total

1.  Adrenoleucodystrophy: a molecular genetic study in five families.

Authors:  R G Del Mastro; S Bundey; M W Kilpatrick
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

2.  Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis.

Authors:  B A van Oost; P M van Zandvoort; W Tünte; H G Brunner; A J Hoogeboom; P D Maaswinkel-Mooy; J Bakkeren; B Hamel; H H Ropers
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

Review 3.  Inherited peroxisomal disorders involving the nervous system.

Authors:  J B Stephenson
Journal:  Arch Dis Child       Date:  1988-07       Impact factor: 3.791

4.  Gonadal mosaicism in a family with adrenoleukodystrophy: molecular diagnosis of carrier status among daughters of a gonadal mosaic when direct detection of the mutation is not possible.

Authors:  G E Graham; P M MacLeod; D P Lillicrap; P J Bridge
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

5.  Normal and abnormal color-vision genes.

Authors:  A G Motulsky
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

6.  Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.

Authors:  G H Sack; M Alpern; T Webster; R P Feil; J C Morrell; G Chen; W Chen; C T Caskey; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

Review 7.  DNA diagnosis of X-linked adrenoleukodystrophy.

Authors:  S Seneca; W Lissens
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

Review 8.  Adrenoleukodystrophy: phenotypic variability and implications for therapy.

Authors:  H W Moser; A B Moser; K D Smith; A Bergin; J Borel; J Shankroff; O C Stine; C Merette; J Ott; W Krivit
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

9.  Color vision defects in adrenomyeloneuropathy.

Authors:  G H Sack; M B Raven; H W Moser
Journal:  Am J Hum Genet       Date:  1989-06       Impact factor: 11.025

10.  Carrier detection in X-linked adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis.

Authors:  L D Notarangelo; O Parolini; G Baiguini; F Buzi; C Paterlini; A Perini; M Rimoldi; S Tiberti; G Uziel; L Notarangelo
Journal:  Eur J Pediatr       Date:  1992-10       Impact factor: 3.183

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