Literature DB >> 3014445

NcoI RFLP at the human apolipoprotein CII gene locus.

P M Frossard, R T Coleman, G Assmann.   

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Year:  1986        PMID: 3014445      PMCID: PMC311522          DOI: 10.1093/nar/14.12.5120

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


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  1 in total

1.  Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.

Authors:  C L Jackson; G A Bruns; J L Breslow
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

  1 in total
  6 in total

1.  A polymorphic PstI site in intron 2 of the human apolipoprotein C-II gene detected by polymerase chain reaction.

Authors:  B R Zysow; C R Pullinger; J P Kane
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  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

3.  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

4.  Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides.

Authors:  B Smeets; J Poddighe; H Brunner; H H Ropers; B Wieringa
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

5.  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

6.  Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.

Authors:  P Nokelainen; L Alanen-Kurki; R Winqvist; B Falck; H Somer; J Leisti; K Johnson; M L Savontaus; L Peltonen
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

  6 in total

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