Literature DB >> 1975676

RsaI polymorphism in von Willebrand factor (vWF) at codon 789.

G R Kunkel1, J B Graham, D M Fowlkes, S T Lord.   

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Year:  1990        PMID： 1975676      PMCID： PMC332029          DOI： 10.1093/nar/18.16.4961-a

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


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  1 in total

1.  The Malmö polymorphism of factor IX: establishing the genotypes by rapid analysis of DNA.

Authors:  J B Graham; G R Kunkel; G S Tennyson; S T Lord; D M Fowlkes
Journal:  Blood       Date:  1989-06       Impact factor: 22.113
  1 in total
  9 in total

1.  Testing the feasibility of DNA typing for human identification by PCR and an oligonucleotide ligation assay.

Authors:  C Delahunty; W Ankener; Q Deng; J Eng; D A Nickerson
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Severe von Willebrand disease due to a defect at the level of von Willebrand factor mRNA expression: detection by exonic PCR-restriction fragment length polymorphism analysis.

Authors:  W C Nichols; S E Lyons; J S Harrison; R L Cody; D Ginsburg
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-01       Impact factor: 11.205

3.  The varying frequencies of five DNA polymorphisms of X-linked coagulant factor IX in eight ethnic groups.

Authors:  J B Graham; G R Kunkel; N K Egilmez; A Wallmark; D M Fowlkes; S T Lord
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

4.  Linkage disequilibrium patterns vary with chromosomal location: a case study from the von Willebrand factor region.

Authors:  W S Watkins; R Zenger; E O'Brien; D Nyman; A W Eriksson; M Renlund; L B Jorde
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

5.  Polymorphisms of PAI-1 and platelet GP Ia may associate with impairment of renal function and thrombocytopenia in Puumala hantavirus infection.

Authors:  Outi Laine; Lotta Joutsi-Korhonen; Satu Mäkelä; Jussi Mikkelsson; Tanja Pessi; Sari Tuomisto; Heini Huhtala; Daniel Libraty; Antti Vaheri; Pekka Karhunen; Jukka Mustonen
Journal:  Thromb Res       Date:  2011-11-30       Impact factor: 3.944

Review 6.  [Possible genetic causes for late complications of diabetes mellitus].

Authors:  T Klemm; R Paschke
Journal:  Med Klin (Munich)       Date:  2000-01-15

7.  Classification of exon 18 linked variants of VWF gene in von Willebrand disease.

Authors:  Shirin Shahbazi; Sara Alavi; Reza Mahdian
Journal:  Int J Mol Epidemiol Genet       Date:  2012-02-29

8.  Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.

Authors:  Jill M Johnsen; Paul L Auer; Alanna C Morrison; Shuo Jiao; Peng Wei; Jeffrey Haessler; Keolu Fox; Sean R McGee; Joshua D Smith; Christopher S Carlson; Nicholas Smith; Eric Boerwinkle; Charles Kooperberg; Deborah A Nickerson; Stephen S Rich; David Green; Ulrike Peters; Mary Cushman; Alex P Reiner
Journal:  Blood       Date:  2013-05-20       Impact factor: 22.113

9.  Identification of a candidate missense mutation in a family with von Willebrand disease type IIC.

Authors:  R Schneppenheim; K B Thomas; S Krey; U Budde; U Jessat; A H Sutor; B Zieger
Journal:  Hum Genet       Date:  1995-06       Impact factor: 4.132
  9 in total

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