Zobrazeno 1 - 10
of 28
pro vyhledávání: '"J. M. Gonzalez-Redondo"'
Autor:
K. McKie, Abdullah Kutlar, E. Baysal, Virgil McKie, Ferdane Kutlar, Titus H.J. Huisman, J. M. Gonzalez-Redondo
Publikováno v:
American journal of hematology. 38(1)
An extension of previous reports describing the molecular defects and hematological abnormalities in black patients with Hb S(C) beta-thalassemia living in the Southeastern United States is presented. As many as 58 patients with Hb S-beta(+)-thalasse
Autor:
J. M. Gonzalez-Redondo, O. Josifovska, Titus H.J. Huisman, N. Nikolov, J. F. Codrington, Georgi D. Efremov, C. Oner
Publikováno v:
British journal of haematology. 75(2)
Hb Icaria-Hb H disease was observed in a Yugoslavian teenager who exhibited moderate anaemia with severe microcytosis and hypochromia and 16% Hb H. Four of his relatives were Hb Icaria heterozygotes; their haematological data were comparable to those
Autor:
Abdullah Kutlar, A. L. Reese, Titus H.J. Huisman, G. Cheng, Ferdane Kutlar, Christos Kattamis, H. Hu, J. M. Gonzalez-Redondo
Publikováno v:
British journal of haematology. 74(3)
The mutations producing beta-thalassaemia in 174 Greek patients with thalassaemia major were investigated by dot-blot hybridization of oligonucleotide probes to genomic DNA amplified by the polymerase chain reaction procedure, by direct sequencing of
Publikováno v:
Annals of the New York Academy of Sciences. 565:398-401
Publikováno v:
Biochemical and Biophysical Research Communications. 163:8-13
Hemoglobin Malay (alpha 2 beta 2 19 Asn----Ser) has been observed in a few Malaysian patients with thalassemia intermedia. The beta Malay substitution increases the homology of the cryptic splice site at codons 17/18/19 of the beta-globin gene to the
Publikováno v:
Biochemical Genetics. 26:207-211
We have cloned and sequenced the human θ1-globin gene. The nucleotide sequence and organization of the human θ1 gene (exons, introns, promoter, and polyadenylation signals) are similar to those reported for the orangutan θ1-globin gene. If these g
Autor:
Kenneth D. Lanclos, Abdullah Kutlar, T. A. Stoming, B Deng, Ferdane Kutlar, Y.C. Gu, T. Nakatsuji, Virgil McKie, J. M. Gonzalez-Redondo, I. S. Han
Publikováno v:
Blood. 72:1007-1014
The presence of various substitutions and deletions resulting in beta- thalassemia was studied in 19 black patients with homozygous beta- thalassemia and in numerous relatives; all patients were from Georgia, South Carolina, and Alabama. Methodology
Autor:
H. Hu, Titus H.J. Huisman, Ferdane Kutlar, J. B. Wilson, Abdullah Kutlar, T. A. Stoming, J. M. Gonzalez-Redondo
Publikováno v:
Hemoglobin. 13:67-74
Autor:
Abdullah Kutlar, J. M. Gonzalez Redondo, J. B. Wilson, Titus H.J. Huisman, Ferdane Kutlar, Brooke B. Webber
Publikováno v:
Hemoglobin. 11:185-188
Autor:
M. I. Balda-Aguirre, J. J. Malcorra-Azpiazu, J. C. Diaz-Chico, Titus H.J. Huisman, J. M. Gonzalez-Redondo
Publikováno v:
British Journal of Haematology. 70:459-463
A new deletion of more than 27 kb, removing the psi zeta 1, psi alpha 2, psi alpha 1, alpha 2, alpha 1 and theta 1 globin genes has been found in four members of a Spanish family, including two patients with Hb H disease. The 5' end point of the dele