Literature DB >> 9643300

Microsatellite markers for the cone-rod retinal dystrophy gene, CRX, on 19q13.3.

J Bellingham, C Y Gregory-Evans, K Gregory-Evans.   

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Year:  1998        PMID： 9643300      PMCID： PMC1051356          DOI： 10.1136/jmg.35.6.527

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  12 in total

1.  Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.

Authors:  R Fujita; M Buraczynska; L Gieser; W Wu; P Forsythe; M Abrahamson; S G Jacobson; P A Sieving; S Andréasson; A Swaroop
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

2.  Yeast artificial chromosome libraries containing large inserts from mouse and human DNA.

Authors:  Z Larin; A P Monaco; H Lehrach
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-15       Impact factor: 11.205

3.  A comprehensive genetic map of the human genome based on 5,264 microsatellites.

Authors:  C Dib; S Fauré; C Fizames; D Samson; N Drouot; A Vignal; P Millasseau; S Marc; J Hazan; E Seboun; M Lathrop; G Gyapay; J Morissette; J Weissenbach
Journal:  Nature       Date:  1996-03-14       Impact factor: 49.962

4.  Refinement of the cone-rod retinal dystrophy locus on chromosome 19q.

Authors:  C Y Gregory; K Evans; J L Whittaker; A Fryer; J Weissenbach; S S Bhattacharya
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

5.  Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.

Authors:  T Furukawa; E M Morrow; C L Cepko
Journal:  Cell       Date:  1997-11-14       Impact factor: 41.582

6.  Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.

Authors:  C L Freund; C Y Gregory-Evans; T Furukawa; M Papaioannou; J Looser; L Ploder; J Bellingham; D Ng; J A Herbrick; A Duncan; S W Scherer; L C Tsui; A Loutradis-Anagnostou; S G Jacobson; C L Cepko; S S Bhattacharya; R R McInnes
Journal:  Cell       Date:  1997-11-14       Impact factor: 41.582

7.  Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypes.

Authors:  S D Wijesuriya; K Evans; M R Jay; C Davison; B H Weber; A C Bird; S S Bhattacharya; C Y Gregory
Journal:  Genome Res       Date:  1996-02       Impact factor: 9.043

8.  Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion.

Authors:  K Evans; A Fryer; C Inglehearn; J Duvall-Young; J L Whittaker; C Y Gregory; R Butler; N Ebenezer; D M Hunt; S Bhattacharya
Journal:  Nat Genet       Date:  1994-02       Impact factor: 38.330

9.  Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype.

Authors:  K Evans; J Duvall-Young; F W Fitzke; G B Arden; S S Bhattacharya; A C Bird
Journal:  Arch Ophthalmol       Date:  1995-02

10.  A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3).

Authors:  A Meindl; K Dry; K Herrmann; F Manson; A Ciccodicola; A Edgar; M R Carvalho; H Achatz; H Hellebrand; A Lennon; C Migliaccio; K Porter; E Zrenner; A Bird; M Jay; B Lorenz; B Wittwer; M D'Urso; T Meitinger; A Wright
Journal:  Nat Genet       Date:  1996-05       Impact factor: 38.330
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