Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M G Hadjiminas"'
Autor:
George Stamatoyannopoulos, Yuet Wai Kan, M. G. Hadjiminas, Michel Goossens, Andrée M. Dozy, Stephen H. Embury, Z. Zachariades
Publikováno v:
Proceedings of the National Academy of Sciences. 77:518-521
We have identified 12 individuals who are heterozygous for a chromosome with three alpha-globin genes. We determined the presence of the third alpha-globin locus by restriction endonuclease digestion and hybridization with alpha-globin cDNA probes. T
Autor:
Antonio Cao, C. Rosatelli, George Stamatoyannopoulos, Mario Furbetta, Andrέe M. Dozy, Mario Pirastu, Z. Zachariades, M. G. Hadjiminas, A Angius, Kathleen Y. Lee, Yuet Wai Kan
Publikováno v:
Scopus-Elsevier
We used restriction endonuclease analysis to determine the incidence of alpha-thalassemia in two Mediterranean islands. In a random population sample, the gene frequency of deletion-type alpha-thalassemia-2 (- alpha) was 0.18 in Sardinians and 0.07 i
Autor:
Yuet Wai Kan, Mario Furbetta, M. G. Hadjiminas, A.M. Dozy, Antonio Cao, Z. Zachariades, George Stamatoyannopoulos
Publikováno v:
Blood. 54:1434-1438
We investigated the molecular basis of hemoglobin-H disease by hybridization and restriction endonuclease mapping of the DNA in the Mediterranean populations. Of the 12 patients studied from Cyprus and Sardinia, 8 had the typical deletion defect with
Autor:
M G Hadjiminas, B. Aldridge, David J. Weatherall, Doug Higgs, J. B. Clegg, Antonio Cao, C Kattamis, L. Pressley, E A Rachmilewitz, A Metaxatou-Mavromati, T Sophocleous
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 78(9)
Restriction endonuclease mapping of nondeletion alpha-thalassemia determinants from a variety of racial groups showed no detectable abnormalities within a 40-kilobase region of the zeta-alpha globin gene cluster. By using a zeta-specific probe, we de
Autor:
M, Pirastu, K Y, Lee, A M, Dozy, Y W, Kan, G, Stamatoyannopoulos, M G, Hadjiminas, Z, Zachariades, A, Angius, M, Furbetta, C, Rosatelli, A, Cao
Publikováno v:
Blood. 60(2)
We used restriction endonuclease analysis to determine the incidence of alpha-thalassemia in two Mediterranean islands. In a random population sample, the gene frequency of deletion-type alpha-thalassemia-2 (-alpha) was 0.18 in Sardinians and 0.07 in
Autor:
Y W, Kan, A M, Dozy, G, Stamatoyannopoulos, M G, Hadjiminas, Z, Zachariades, M, Furbetta, A, Cao
Publikováno v:
Blood. 54(6)
We investigated the molecular basis of hemoglobin-H disease by hybridization and restriction endonuclease mapping of the DNA in the Mediterranean populations. Of the 12 patients studied from Cyprus and Sardinia, 8 had the typical deletion defect with
Publikováno v:
Pediatric Research. 24:412-412
Y. enterocolitica requires iron for growth making thalassaemic chilren susceptible to infections with this organism. In order to investigate the hypothesis that a common mucosal immune system exists in man, serum and salivary antibodies to Y.enteroco