Literature DB >> 2901730

NcoI RFLP at the creatine kinase-muscle type gene locus (CKMM, chromosome 19).

M Coerwinkel-Driessen1, J Schepens, P van Zandvoort, B van Oost, E Mariman, B Wieringa.   

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Year:  1988        PMID： 2901730      PMCID： PMC338621          DOI： 10.1093/nar/16.17.8743

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

1.  Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome.

Authors:  T Hulsebos; B Wieringa; R Hochstenbach; D Smeets; J Schepens; F Oerlemans; J Zimmer; H H Ropers
Journal:  Cytogenet Cell Genet       Date:  1986
  1 in total
  12 in total

1.  Muscle-specific creatine kinase gene polymorphism and running economy responses to an 18-week 5000-m training programme.

Authors:  D Q Zhou; Y Hu; G Liu; L Gong; Y Xi; L Wen
Journal:  Br J Sports Med       Date:  2006-09-25       Impact factor: 13.800

2.  Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy.

Authors:  H J Smeets; H G Brunner; H H Ropers; B Wieringa
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

3.  Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms.

Authors:  J Bailly; A E MacKenzie; S Leblond; R G Korneluk
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

4.  Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).

Authors:  H G Brunner; R G Korneluk; M Coerwinkel-Driessen; A MacKenzie; H Smeets; H M Lambermon; B A van Oost; B Wieringa; H H Ropers
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

5.  A molecular and cytogenetic study in Finnish Prader-Willi patients.

Authors:  H Kokkonen; M Kähkönen; J Leisti
Journal:  Hum Genet       Date:  1995-05       Impact factor: 4.132

6.  Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish population.

Authors:  A Cobo; D Grinberg; S Balcells; L Vilageliu; R Gonzàlez-Duarte; M Baiget
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

7.  The 1.5-Mb region spanning the myotonic dystrophy locus shows uniform recombination frequency.

Authors:  G G Shutler; A E MacKenzie; R G Korneluk
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

8.  A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes.

Authors:  H Smeets; L Bachinski; M Coerwinkel; J Schepens; J Hoeijmakers; M van Duin; K H Grzeschik; C A Weber; P de Jong; M J Siciliano
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

9.  The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.

Authors:  A E MacKenzie; R G Korneluk; F Zorzato; J Fujii; M Phillips; D Iles; B Wieringa; S Leblond; J Bailly; H F Willard
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

10.  A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.

Authors:  K Johnson; P Shelbourne; J Davies; J Buxton; E Nimmo; M J Siciliano; L L Bachinski; M Anvret; H Harley; S Rundle
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025
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