Literature DB >> 8314593

Exon structure of the human dystrophin gene.

R G Roberts1, A J Coffey, M Bobrow, D R Bentley.   

Abstract

Application of a novel vectorette PCR approach to defining intron-exon boundaries has permitted completion of analysis of the exon structure of the largest and most complex known human gene. We present here a summary of the exon structure of the entire human dystrophin gene, together with the sizes of genomic HindIII fragments recognized by each exon, and (where available) GenBank accession numbers for adjacent intron sequences.

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Year:  1993        PMID: 8314593     DOI: 10.1006/geno.1993.1225

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  41 in total

1.  Deletional mutations of dystrophin gene and carrier detection in eastern India.

Authors:  Jayasri Basak; Uma B Dasgupta; Subhash Chandra Mukherjee; Shyamal Kumar Das; Asit Kumar Senapati; Tapas Kumar Banerjee
Journal:  Indian J Pediatr       Date:  2009-11-12       Impact factor: 1.967

Review 2.  [Molecular pathogenesis of muscular diseases].

Authors:  K Ohlendieck
Journal:  Naturwissenschaften       Date:  1996-12

3.  Stability of the human dystrophin transcript in muscle.

Authors:  C N Tennyson; Q Shi; R G Worton
Journal:  Nucleic Acids Res       Date:  1996-08-01       Impact factor: 16.971

4.  A muscle-specific enhancer within intron 1 of the human dystrophin gene is functionally dependent on single MEF-1/E box and MEF-2/AT-rich sequence motifs.

Authors:  H J Klamut; L O Bosnoyan-Collins; R G Worton; P N Ray
Journal:  Nucleic Acids Res       Date:  1997-04-15       Impact factor: 16.971

5.  IRBIS: a systematic search for conserved complementarity.

Authors:  Dmitri D Pervouchine
Journal:  RNA       Date:  2014-08-20       Impact factor: 4.942

6.  Analysis of the functional consequences of targeted exon deletion in COL7A1 reveals prospects for dystrophic epidermolysis bullosa therapy.

Authors:  Olivier Bornert; Tobias Kühl; Jeroen Bremer; Peter C van den Akker; Anna Mg Pasmooij; Alexander Nyström
Journal:  Mol Ther       Date:  2016-05-09       Impact factor: 11.454

Review 7.  Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.

Authors:  N Cohen; F Muntoni
Journal:  Heart       Date:  2004-08       Impact factor: 5.994

8.  Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.

Authors:  E Pegoraro; R N Schimke; K Arahata; Y Hayashi; H Stern; H Marks; M R Glasberg; J E Carroll; J W Taber; H B Wessel
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

9.  Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophy.

Authors:  D J Bunyan; D O Robinson; A L Collins; A E Cockwell; H M Bullman; P A Whittaker
Journal:  Hum Genet       Date:  1994-05       Impact factor: 4.132

10.  Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter.

Authors:  H Nishio; Y Takeshima; N Narita; H Yanagawa; Y Suzuki; Y Ishikawa; Y Ishikawa; R Minami; H Nakamura; M Matsuo
Journal:  J Clin Invest       Date:  1994-09       Impact factor: 14.808

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