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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

76 related articles for article (PubMed ID: 1752248)

  • 21. The esterase D polymorphism by ultrathin layer isoelectric-focusing: frequency of the EsD5 allele in the population of Rome.
    Ranalletta D; Destro-Bisol G; Fucci N
    Anthropol Anz; 1987 Jun; 45(2):153-7. PubMed ID: 3619413
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A new method for FXIIIA genetic variants determination using isoelectric focusing in 1 M urea. Evidence for three structural gene loci, FXIIIA1, FXIIIA2, and FXIIIA3.
    Sebetan IM
    Hum Genet; 1988 Dec; 81(1):95-7. PubMed ID: 2904408
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Activity and levels of factor XIII in a Venezuelan admixed population: association with rs5985 (Val35Leu) and STR F13A01 polymorphisms.
    Vívenes M; Castro de Guerra D; Rodríguez-Larralde A; Arocha-Piñango CL; Guerrero B
    Thromb Res; 2012 Nov; 130(5):729-34. PubMed ID: 22909824
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic polymorphism of coagulation factor XIII B subunit in the Japanese population: description of three new rare alleles.
    Nakamura S; Ohue O; Abe K
    Hum Genet; 1986 Jun; 73(2):183-5. PubMed ID: 3721505
    [TBL] [Abstract][Full Text] [Related]  

  • 25. C3 polymorphism and NADH diaphorase types in Sardinia (Italy).
    Floris Masala R; Mameli GE; Succa V; Vona G
    Gene Geogr; 1990 Apr; 4(1):35-41. PubMed ID: 2278901
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Distribution of ORM1, C6, C7 and APO C-II allele frequencies in populations from mainland Italy and Sardinia.
    Scacchi R; Corbo RM; Cossu G; Mureddu L; Mulas G; Pascone R
    Hum Hered; 1992; 42(5):309-15. PubMed ID: 1459576
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic heterogeneity of factor XIII deficiency: first description of unstable A subunits.
    Castle S; Board PG; Anderson RA
    Br J Haematol; 1981 Jun; 48(2):337-42. PubMed ID: 7236530
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Variability of the CD4 and F13A1 short tandem repeats in Corsicans, Sardinians and Piaroa Indians.
    Vona G; Calò CM; Mameli GE; Marini E; Morelli L; Succa V; Casula S; Ristaldi MS
    Gene Geogr; 1996 Apr; 10(1):51-63. PubMed ID: 8913722
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Improved coagulation factor XIII B (FXIIIB) phenotyping after neuraminidase treatment of plasma and first description of the FXIIIB 2 phenotype.
    Kreckel P; Kühnl P
    Blut; 1982 Nov; 45(5):337-45. PubMed ID: 7139131
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic and phenotypic polymorphisms of the A subunit of Coagulation factor XIII in Japanese population.
    Taniguchi M; Ayabe T; Ashida T; Fujimoto Y; Kohgo Y
    Biochem Genet; 2002 Oct; 40(9-10):339-49. PubMed ID: 12392171
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The effect of the Val34Leu polymorphism in the factor XIII gene in infants with a birth weight below 1500 g.
    Göpel W; Kattner E; Seidenberg J; Kohlmann T; Segerer H; Möller J;
    J Pediatr; 2002 Jun; 140(6):688-92. PubMed ID: 12072871
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Polymorphisms of serum proteins in Japanese patients with vascular diseases. I. Factor XIIIB, plasminogen and complement types in primary varicose veins.
    Mizutani K; Nishimukai H; Yasugi T; Iwahashi K; Tsunekawa K; Shinomiya T
    Hum Hered; 1991; 41(4):270-5. PubMed ID: 1783414
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hemopoietic origin of factor XIII A subunits in platelets, monocytes, and plasma. Evidence from bone marrow transplantation studies.
    Poon MC; Russell JA; Low S; Sinclair GD; Jones AR; Blahey W; Ruether BA; Hoar DI
    J Clin Invest; 1989 Sep; 84(3):787-92. PubMed ID: 2569478
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic polymorphism of coagulation factor XIIIB subunit in Japanese.
    Nakamura S; Abe K
    Ann Hum Genet; 1982 Jul; 46(3):203-7. PubMed ID: 7125593
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic polymorphism of the A subunit of human coagulation factor XIII in Japanese.
    Nishigaki T; Omoto K; Juji T
    Jinrui Idengaku Zasshi; 1981 Sep; 26(3):237-41. PubMed ID: 6121068
    [No Abstract]   [Full Text] [Related]  

  • 36. Alpha 2 HS-glycoprotein phenotype and allele distribution in continental Italy and Sardinia.
    Scacchi R; Lucarelli P; Corbo RM
    Hum Hered; 1989; 39(1):52-4. PubMed ID: 2759626
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic studies of low-abundance human plasma proteins. X. Coagulation factor XIIIB variants in blacks.
    Kamboh MI; Ferrell RE
    Electrophoresis; 1989 Jan; 10(1):53-7. PubMed ID: 2714240
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Population genetics and the coagulation factor XIII A polymorphism].
    Rittner C; Wolf T
    Z Rechtsmed; 1984; 91(3):225-9. PubMed ID: 6702319
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic polymorphism of the A subunit of human coagulation factor XIII in Japanese.
    Kera Y; Nishimukai H
    Hum Hered; 1982; 32(3):216-8. PubMed ID: 6125470
    [No Abstract]   [Full Text] [Related]  

  • 40. Molecular basis for subtypic differences of the "a" subunit of coagulation factor XIII with description of the genesis of the subtypes.
    Suzuki K; Iwata M; Ito S; Matsui K; Uchida A; Mizoi Y
    Hum Genet; 1994 Aug; 94(2):129-35. PubMed ID: 7913909
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.