Zobrazeno 1 - 10
of 702
pro vyhledávání: '"Barton James C"'
Autor:
Barton, James C.1,2,3 (AUTHOR) bartonjames336@gmail.com, Barton, J. Clayborn2 (AUTHOR), Bertoli, Luigi F.2,3 (AUTHOR), Acton, Ronald T.2,4 (AUTHOR)
Publikováno v:
PLoS ONE. 5/14/2024, Vol. 19 Issue 5, p1-14. 14p.
Publikováno v:
BMC Medical Genetics, Vol 7, Iss 1, p 22 (2006)
Abstract Background In age-matched cohorts of screening study participants recruited from primary care clinics, mean serum transferrin saturation values were significantly lower and mean serum ferritin concentrations were significantly higher in Nati
Externí odkaz:
https://doaj.org/article/937fa75b7860489eaa7273c0f7ae2339
Publikováno v:
BMC Medical Genetics, Vol 5, Iss 1, p 29 (2004)
Abstract Background Homozygosity or compound heterozygosity for coding region mutations of the hemojuvelin gene (HJV) in whites is a cause of early age-of-onset iron overload (juvenile hemochromatosis), and of hemochromatosis phenotypes in some young
Externí odkaz:
https://doaj.org/article/86387fd752cc4a79921e068983843358
Autor:
Hollowell William W, Barton Ellen H, Acton Ronald T, Dreibelbis Amy L, Go Rodney CP, Barton James C
Publikováno v:
BMC Cancer, Vol 4, Iss 1, p 47 (2004)
Abstract Background We sought to evaluate the hypothesis that the high incidence of cutaneous melanoma in white persons in central Alabama is associated with a predominance of Irish and Scots descent. Methods Frequencies of country of ancestry report
Externí odkaz:
https://doaj.org/article/5b4d7b8ea7054f198e97f59c09f6a2ed
Publikováno v:
BMC Cancer, Vol 4, Iss 1, p 6 (2004)
Abstract Background We sought to compare frequencies of HFE C282Y and H63D alleles and associated odds ratios (OR) in 100 consecutive unrelated white adults with malignancy to those in 318 controls. Methods Data from patients with more than one malig
Externí odkaz:
https://doaj.org/article/f5a7ec3521b24c7cad065ae580614241
Publikováno v:
BMC Medical Genetics, Vol 4, Iss 1, p 3 (2003)
Abstract Background We wanted to quantify HLA-A and -B phenotype and haplotype frequencies in Alabama index patients with common variable immunodeficiency (CVID) and selective IgG subclass deficiency (IgGSD), and in control subjects. Methods Phenotyp
Externí odkaz:
https://doaj.org/article/84f1b68b414e463d99fedf77be8b095e
Autor:
Barton, James C.1,2 (AUTHOR) bartonjames336@gmail.com, Barton, J. Clayborn2 (AUTHOR), Acton, Ronald T.2,3 (AUTHOR)
Publikováno v:
Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-11. 11p.
Publikováno v:
Platelets. Dec2023, Vol. 34 Issue 1, p1-7. 7p.
Autor:
Barton James C, Acton Ronald T
Publikováno v:
BMC Medical Genetics, Vol 3, Iss 1, p 9 (2002)
Abstract Background We wanted to quantify HLA-A and -B allele and haplotype frequencies in Alabama hemochromatosis probands with HFE C282Y homozygosity and controls, and to compare results to those in other populations. Methods Alleles were detected
Externí odkaz:
https://doaj.org/article/a64c2690ba69429bba0cbef0239b2141