Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Andrée M. Dozy"'
Autor:
Yuet Wai Kan, Andrée M. Dozy
Publikováno v:
Clinical Genetics. 45:221-227
Of the many methods which have been devised to detect point mutations, we use reverse dot blot for beta-thalassemia in our laboratory. In any mutation detection program, rare or new mutations outside of a laboratory's repertoire will be encountered.
Publikováno v:
Advanced Drug Delivery Reviews. 17:227-234
The development of retroviral vectors that target specific cell types could have important implications for the design of gene therapy strategies. A chimeric protein containing the polypeptide hormone erythropoietin and part of the env protein of eco
Publikováno v:
Science (New York, N.Y.). 266(5189)
The development of retroviral vectors that target specific cell types could have important implications for the design of gene therapy strategies. A chimeric protein containing the polypeptide hormone erythropoietin and part of the env protein of eco
Publikováno v:
Human mutation. 3(4)
Publikováno v:
Annals of the New York Academy of Sciences. 612
Publikováno v:
British Journal of Haematology. 46:557-564
The presence of Hb New York was confirmed in a Chinese family in which affected members have occasional red cells with Hb-H-like inclusions and a relative decrease in alpha chain synthesis, suggestive of a coexisting alpha thalassaemia trait. However
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
Publikováno v:
Annals of the New York Academy of Sciences. 344:141-150
Autor:
Andrée M. Dozy, Yuet Wai Kan
Publikováno v:
Science. 209:388-391
A polymorphic HpaI endonuclease recognition site on the 3' side of the beta-globin gene was used to analyze the evolution of the beta-globin gene mutants S and C. Study of the world wide distribution of the normal and variant HpaI sites showed that t
Publikováno v:
Proceedings of the National Academy of Sciences. 72:5140-5144
In two Chinese patients with homozygous beta(0)-thalassemia, messenger RNAs from peripheral blood reticulocytes and the bone marrow failed to direct beta-chain synthesis in vivo and in vitro in a cell-free system. Molecular hybridization showed that