Literature DB >> 8270261

Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32.

J Fitzgibbon1, B Appukuttan, S Gayther, D Wells, J Delhanty, D M Hunt.   

Abstract

Blue cone pigment (BCP) is one of three types of cone photoreceptors responsible for normal colour vision. In this study, the BCP gene has been localised to chromosome 7q31.3-32 by fluorescent in situ hybridisation of cosmid clones containing the gene. This is consistent with previous mapping of the BCP gene to chromosome 7q31-35.

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Year:  1994        PMID： 8270261     DOI： 10.1007/bf00218919

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  12 in total

1.  Autosomal dominantly inherited macular dystrophy with preferential short-wavelength sensitive cone involvement.

Authors:  G H Bresnick; V C Smith; J Pokorny
Journal:  Am J Ophthalmol       Date:  1989-09-15       Impact factor: 5.258

2.  Late onset dominant cone dystrophy with early blue cone involvement.

Authors:  L N Went; M J van Schooneveld; J A Oosterhuis
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

3.  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

4.  A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

Authors:  T P Dryja; T L McGee; E Reichel; L B Hahn; G S Cowley; D W Yandell; M A Sandberg; E L Berson
Journal:  Nature       Date:  1990-01-25       Impact factor: 49.962

5.  An electroretinographic and molecular genetic study of X-linked cone degeneration.

Authors:  E Reichel; A M Bruce; M A Sandberg; E L Berson
Journal:  Am J Ophthalmol       Date:  1989-11-15       Impact factor: 5.258

6.  A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.

Authors:  C F Inglehearn; R Bashir; D H Lester; M Jay; A C Bird; S S Bhattacharya
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

7.  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

8.  Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

Authors:  C H Sung; C M Davenport; J C Hennessey; I H Maumenee; S G Jacobson; J R Heckenlively; R Nowakowski; G Fishman; P Gouras; J Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

9.  Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

Authors:  D Pinkel; T Straume; J W Gray
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

10.  Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q.

Authors:  S A Jordan; G J Farrar; P Kenna; M M Humphries; D M Sheils; R Kumar-Singh; E M Sharp; N Soriano; C Ayuso; J Benitez
Journal:  Nat Genet       Date:  1993-05       Impact factor: 38.330
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  2 in total

Review 1.  Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.

Authors:  P J Rosenfeld; V A McKusick; J S Amberger; T P Dryja
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

2.  Localization of the human RGR opsin gene to chromosome 10q23.

Authors:  X N Chen; J R Korenberg; M Jiang; D Shen; H K Fong
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132
  2 in total

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