These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
87 related items for PubMed ID: 7554360
1. A recombination event in the closely linked plasminogen and apolipoprotein(a) gene loci. Magnaghi P, Agazzi A, Semino O, Ferrari M, Barbui T, D'Angelo A, Taramelli R. Clin Genet; 1995 Jun; 47(6):285-9. PubMed ID: 7554360 [Abstract] [Full Text] [Related]
6. Variation in the size of human apolipoprotein(a) is due to a hypervariable region in the gene. Lindahl G, Gersdorf E, Menzel HJ, Seed M, Humphries S, Utermann G. Hum Genet; 1990 May; 84(6):563-7. PubMed ID: 1970974 [Abstract] [Full Text] [Related]
9. DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster. Antonarakis SE, Oettgen P, Chakravarti A, Halloran SL, Hudson RR, Feisee L, Karathanasis SK. Hum Genet; 1988 Nov; 80(3):265-73. PubMed ID: 2903847 [Abstract] [Full Text] [Related]
10. The gene for the Lp(a)-specific glycoprotein is closely linked to the gene for plasminogen on chromosome 6. Lindahl G, Gersdorf E, Menzel HJ, Duba C, Cleve H, Humphries S, Utermann G. Hum Genet; 1989 Jan; 81(2):149-52. PubMed ID: 2521477 [Abstract] [Full Text] [Related]
13. A novel missense mutation in two families with congenital plasminogen deficiency: identification of an Ala675 to Thr675 substitution. Mima N, Azuma H, Shigekiyo T, Saito S. Thromb Haemost; 1996 Jan; 75(1):96-100. PubMed ID: 8713786 [Abstract] [Full Text] [Related]
15. Characterization by yeast artificial chromosome cloning of the linked apolipoprotein(a) and plasminogen genes and identification of the apolipoprotein(a) 5' flanking region. Malgaretti N, Acquati F, Magnaghi P, Bruno L, Pontoglio M, Rocchi M, Saccone S, Della Valle G, D'Urso M, LePaslier D. Proc Natl Acad Sci U S A; 1992 Dec 01; 89(23):11584-8. PubMed ID: 1454851 [Abstract] [Full Text] [Related]
16. Two restriction fragment length polymorphisms at the apolipoprotein AIV (apoAIV) locus. Martín I, Añíbarro C, Cenarro A, Polanco JI, Pocoví M, Rodríguez-Rey JC. Mol Cell Probes; 1995 Oct 01; 9(5):371-2. PubMed ID: 8569779 [No Abstract] [Full Text] [Related]
20. A K19E missense mutation in the plasminogen gene is a common cause of familial hypoplasminogenaemia. Tefs K, Tait CR, Walker ID, Pietzsch N, Ziegler M, Schuster V. Blood Coagul Fibrinolysis; 2003 Jun 01; 14(4):411-6. PubMed ID: 12945885 [Abstract] [Full Text] [Related] Page: [Next] [New Search]